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2015v1.0
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Brian Kloss, DO, JD, PA-C
Associate Professor
Department of Emergency Medicine
SUNY Upstate Medical University
Syracuse, New York
No part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical,
including photocopying, recording, or any information storage and retrieval system, without permission in writing from
the publisher. Details on how to seek permission, further information about the Publisher’s permissions policies and our
arrangements with organizations such as the Copyright Clearance Center and the Copyright Licensing Agency, can be
found at our website: www.elsevier.com/permissions.
This book and the individual contributions contained in it are protected under copyright by the Publisher (other than as
may be noted herein).
Notices
Knowledge and best practice in this field are constantly changing. As new research and experience broaden our
understanding, changes in research methods, professional practices, or medical treatment may become necessary.
Practitioners and researchers must always rely on their own experience and knowledge in evaluating and using
any information, methods, compounds, or experiments described herein. In using such information or methods they
should be mindful of their own safety and the safety of others, including parties for whom they have a professional
responsibility.
With respect to any drug or pharmaceutical products identified, readers are advised to check the most current
information provided (i) on procedures featured or (ii) by the manufacturer of each product to be administered,
to verify the recommended dose or formula, the method and duration of administration, and contraindications.
It is the responsibility of practitioners, relying on their own experience and knowledge of their patients, to make
diagnoses, to determine dosages and the best treatment for each individual patient, and to take all appropriate
safety precautions.
To the fullest extent of the law, neither the Publisher nor the authors, contributors, or editors, assume any liability
for any injury and/or damage to persons or property as a matter of products liability, negligence or otherwise, or
from any use or operation of any methods, products, instructions, or ideas contained in the material herein.
Printed in China
The authors would like to thank our friends, family, and all the staff at Elsevier for their support.
Thanks to Alex Seldes and Sabre Mrkva for being great friends and permitting us to draw Cleo with all those pediatric illnesses.
Thanks to Karen Cyndari, MD/PhD candidate, for website development and support. Thanks to Kara Welch and David
Rothman for assistance with the references and suggested reading section.
Very special thanks to Zubin Damania, MD, a.k.a. ZDoggMD, for making a cameo in our Zika Fever illustration; Mike Cadogan,
MD, from the Life in the Fastlane Emergency Medicine website and blog for making a cameo in our Melioidosis illustration;
and Jawad Kassem, MD, for making a cameo in our Middle Eastern Respiratory Syndrome illustration. Lastly, many thanks to
Rob Guillory, Eisner Award-winning comic book artist for Chew, for his support and serving as a guest illustrator for our Avian
Flu illustration. The guest appearances, celebrity cameos, and pop culture references contained in this textbook are intended to
be works of satire and parody.
vii
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INTRODUCTION
Kloss and Bruce combine real medical education with comic book–style illustrations to create beautiful artistic images that
enhance learning. Realizing that many medical professionals are visual learners, Kloss and Bruce enhance learning by breaking
down complex medical conditions and diseases into illustrated scenes. As children of the eighties and with a passion for comic
books, pop culture, nostalgia, and humor, their illustrations exceed boundaries set by other medical illustrations. Irreverent,
provocative, and unconventional are terms that have been used to describe their campy, tongue-in-cheek approach to medical
education. Their visual aids are colorful, comical, and boundary pushing, all of which make learning more fun and memorable.
Dr. Brian Kloss, a professor and emergency medicine physician, and Travis Bruce, a talented illustrator and designer, aim to
educate physicians, physician assistants, nurses, medical students, and other healthcare providers using humor and comic
book–style illustrations.
Their process is simple. First, Dr. Kloss pencils a rough draft of a medical syndrome, disease, or illness and hands it over to
Travis. Travis then draws out the illustration and adds clarity and color. The end result is a helpful educational tool that is both
comical and informative.
The dynamic duo has been collaborating since connecting at a house party in Brooklyn during the turn of the century. Their
first educational product, Toxicology in a Box, was published by McGraw-Hill in 2013 and is available in Kindle version
on Amazon.com. Toxicology in a Box is a set of 150 full-color flashcards geared toward teaching medical providers how to
recognize and treat various toxic exposures ranging from the bizarre to the mundane.
Kloss and Bruce, in collaboration with Elsevier, are pleased to present their latest work: Graphic Guide to Infectious Disease. This
body of text and illustrations represents 4 years of late nights, highly caffeinated beverages, deadline extensions, revisions, and
more deadline extensions. While they’re admittedly no Rick and Morty, they needed a few deadline extensions.
Their only request is that you loosen your collar, sit back, relax, and enjoy learning high-yield medicine via a truly unique
medium. Welcome to Kloss and Bruce: Medical Education Through Comic Illustration.
ix
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ABOUT THE AUTHORS
Brian Kloss, DO, JD, PA-C, is an Emergency Medicine Physician and Associate Professor at the SUNY Upstate Medical
University and VA Medical Center in Syracuse, New York. He holds a Certificate in Radiologic Technology from Morristown
Memorial Hospital in New Jersey, an Associate of Science in Chemistry from the County College of Morris, a Bachelor of Science
in Physician Assistant Studies from Gannon University, a Juris Doctor for the University at Buffalo School of Law, and a
Doctor of Osteopathic Medicine from UMDNJ-SOM (Rowan). He completed a postgraduate Physician Assistant Fellowship
in Gastroenterology, is Board Certified in Emergency Medicine, and completed a Wilderness Medicine Fellowship at SUNY
Upstate. Brian likes vintage video games, comic books, action figures, and old-school hip hop.
Travis Bruce is an artist, illustrator, and designer living in Queens, New York. He graduated with a BFA in illustration from
the School of Visual Arts, with a focus on graphic narratives and children’s books. Along with illustration, he has designed
tabletop products and giftware for the past 15 years.
xi
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TABLE OF CONTENTS
xiii
xiv TABLE OF CONTENTS
Reservoir: Humans
Description: HAV is a vaccine-preventable fecal-orally transmitted RNA virus that causes acute
hepatitis. Hepatitis A is never chronic, is often asymptomatic in younger patients,
and causes fulminant hepatic failure in ,1% of cases. Risk factors include travel to
endemic regions, ingestion of contaminated food or water (raw shellfish), work in
day care centers (exposure to feces/diaper changing), close contact with infected
patients, and men who have sex with men.
Signs and Symptoms: Typically, the younger the patient, the fewer symptoms he or she exhibits. Most infants
will show little to no signs of infection, whereas most adults become symptomatic.
Symptomatic patients experience nausea, vomiting, malaise, abdominal pain, and fever
followed by scleral icterus and jaundice several days later. Symptoms often last for less
than 2 months; however, the disease may be prolonged or can relapse over a 6-month
period. Infection confers lifelong immunity.
Diagnostic Testing: Labs will reveal a hepatocellular pattern with ALT/AST elevations ,1000, rising
before an increase in bilirubin and alkaline phosphatase is seen. ALT, being more
specific to the liver, is often higher than AST. IgM rises in acute infection, and IgG
begins to rise in convalescence. Fulminant hepatic failure, a serious consequence of
infection characterized by altered mental status (hepatic encephalopathy) and
elevations of PT/INR, is more common in older patients and those with preexisting
liver disease (chronic hepatitis B and/or C).
Treatments: Supportive. The disease is preventable by two doses of a vaccine given at least
6 months apart. Depending on the manufacturer, the second dose of the vaccine
can be given up to 12 or 18 months after the first dose. Postexposure vaccine can
be given in healthy persons aged 1–40 years within 14 days to prevent infection.
Postexposure immune globulin is recommended within 14 days for unvaccinated
patients with immunodeficiency, chronic liver disease, adults .41 years, and
children ,12 months old.
Pearls: There have been several food-related outbreaks of hepatitis A in the United States.
Five hundred people became ill in 2003 after consuming salsa made with green
onions at a now-bankrupt Mexican food chain restaurant.
2
CHAPTER 1 HEPATITIS A
Hepatitis A
IgM IgG
3
PART 1 VIRAL HEPATITIS
Reservoir: Humans
Description: HBV is a double-stranded DNA virus that causes acute and chronic hepatitis. The
disease can be transmitted vertically at birth or through contact with infected
bodily fluids, such as blood, semen, and vaginal secretions. Hepatitis B can be
transmitted sexually and through IV drug use. Healthcare workers are at risk of
infection from needlestick injuries.
Signs and Symptoms: Acute: Most infants and young children with acute infections are asymptomatic. Older
patients are more likely to show symptoms, which include fever, malaise, anorexia,
nausea, vomiting, abdominal pain, and jaundice. Approximately 70% of acutely infected
adults will have symptoms. Symptoms can last for several weeks. The incidence of
fulminant hepatic failure is ,1%. Chronic: Chronic hepatitis B is often asymptomatic
but patients can have symptomatic flairs. If untreated, the disease can be spread to
others, cause cirrhosis, and predispose patients to hepatocellular carcinoma. The
likelihood of developing chronic hepatitis B is inversely proportional to age at time of
infection. The risk of vertical transmission is very high and is dependent on the mother’s
HBeAg/HBeAb status. Those women who are HBeAg1 and HBeAb2 are more likely
to pass on the infection. The Centers for Disease Control and Prevention report that
infected newborns develop chronic hepatitis B approximately 90% of the time,
whereas children infected between the ages of 1 and 5 years have a 25%–50% chance
of developing chronic disease. Older children and adults are more likely to clear the
disease and have a 5%–10% chance of chronicity.
Diagnostic Testing: Acute and chronic hepatitis B are diagnosed by specific serum markers and HBV
viral load testing using PCR. Chronic hepatitis B is defined as the presence of HBsAg
detectable in serum for 6 months or longer after symptom onset. Please see our
summary of hepatitis B markers for more information.
Treatments: Treatment of acute disease is supportive, except in cases of fulminant hepatic failure,
wherein nucleoside/nucleotide analog medications are indicated. In chronic hepatitis
B infections, treatment options and the decision to treat are highly dependent on
individual patient factors, such as viral load, presence/absence of cirrhosis or
hepatocellular cancer, HBeAg/HBeAb status, pregnancy status, patient age, and
biochemical markers. Treatment options for chronic hepatitis B include PEGylated
interferon or nucleoside/nucleotide analogs. Nucleoside/nucleotide analogs include
lamivudine, adefovir, entecavir, telbivudine, and tenofovir. The authors recommend
referencing current American Association for the Study of Liver Diseases (AASLD)
and/or European Association for the Study of the Liver (EASL) guidelines prior to
initiating treatment. Hepatitis B is vaccine preventable, and infection after acute
exposure can be prevented with vaccination and immune globulin.
4
CHAPTER 2 HEPATITIS B
Hepatitis B
5
PART 1 VIRAL HEPATITIS
Hepatitis B e Antigen HBeAg is associated with viral replication and is detectable within 6–14 weeks after
(HBeAg): exposure. In chronic hepatitis B, HBeAg serves as a marker of both disease activity
and infectivity. Patients who are HBeAg+ (HBeAb2) have higher viral loads and
greater disease activity and are more infectious. In pregnancy, HBsAg+ women are
more likely to pass the infection on to their infants. Any infant born to a mother
with chronic HBV should be vaccinated and given immune globulin, ideally within
12 hours.
Hepatitis B Virus Core HBcAb is the first antibody to be detected via serum. Although there is a core
Antibody (HBcAb): antigen, it is intracellular and cannot be detected in serum. HBcAb exists as both
IgM (signifying acute infection or significant reactivation of chronic disease) and IgG
(indicating a past exposure to the hepatitis B disease). Because HBcAb can only exist
in those exposed to the disease, it is used when screening donated blood and/or
distinguishing whether a person is immune from disease exposure or vaccination.
Because the HBV vaccine consists only of HBsAg, those patients who have been
successfully vaccinated will test HBsAb1 and HBcAb2. This indicates that they have
antibodies to the hepatitis B surface antigen but have never been exposed to the full
virus. Patients who are HBsAb1 and HBcAb1 have been exposed to the full hepatitis B
virus, had the disease to some extent, and are now immune.
Hepatitis B e Antibody Antibodies to the e antigen are associated with decreased viral loads and herald
(HBeAb): convalescence. Seroconversion to HBeAb occurs early in acute disease but can be
delayed for years in chronic infection. Those patients with chronic hepatitis B that
are HBeAb2 seroconvert to HBeAb1 at a rate of approximately 0.5% per year.
HBsAb: HBsAb confirms immunity, either via vaccination or resolved infection. HBsAb begins
to elevate after HBsAg levels taper off. Again, presence of HBsAg and absence of
HBsAb at 6 months indicates chronic infection. In some cases, there is a window when
neither HBsAg nor HBsAb can be detected. In this case an HBcAb IgM level can be
obtained to evaluate for acute infection.
Hepatitis B Serum DNA: PCR can be used in either a qualitative (yes or no) or quantitative (How much?)
fashion when determining the presence or absence of HBV DNA in serum samples.
In patients who contract HBV infection and seroconvert to an HBsAb1 state, HBV
DNA should be 100% cleared from their serum. Those patients with chronic hepatitis
B will have detectable HBV DNA in their serum, the amount highly dependent on
their HBeAg/HBeAb status. HBV DNA quantitative studies, HBeAg/HBeAb status,
and liver biopsy results (to grade liver damage) are important in determining
treatment eligibility and options.
6
CHAPTER 3 HEPATITIS B SERUM MARKERS
Hepatitis B Markers
C
(Core) He
pB
eAb
E sAb
(Earth) pB
He
S
(Surface)
7
PART 1 VIRAL HEPATITIS
Reservoir: Humans
Description: HCV is a single-stranded RNA virus responsible for both acute and chronic viral
hepatitis, with up to 85% of infections becoming chronic. Risk factors for HCV
transmission include IV drug use, blood transfusions and organ transplantation
before July 2012, receiving clotting factors before 1987, intranasal drug use (cocaine),
long-term hemodialysis, unsterile tattoos (e.g., prison), and vertical transmission.
Sexual and household transmission can occur but is low.
Signs and Symptoms: Acute: Approximately 85% of acute infections are asymptomatic, and about 85% of
hepatitis C infections become chronic. Acute symptoms can include malaise, fatigue,
nausea, vomiting, abdominal pain, and jaundice. Chronic: Often asymptomatic but
can cause malaise and fatigue. People with chronic HCV infections can develop
cirrhosis and are predisposed to developing primary hepatocellular carcinoma.
Extrahepatic manifestations of chronic HCV can include diabetes, cryoglobulinemia,
and glomuleronephritis.
Diagnostic Testing: People with chronic hepatitis C may have normal liver enzymes. Hepatitis C antibody
testing screens for the disease, and positive results should be followed by PCR testing
for viral load and genotype. Positive HCV antibody tests with negative viral load
may indicate a false-positive antibody test or identify a patient who previously had
hepatitis C and cleared the virus either spontaneously or via treatment.
Treatments: Since the treatment for hepatitis C is continuously evolving, the authors recommend
consulting the American Association for the Study of Liver Disease (AASLD) and/or the
Infectious Disease Society of America (IDSA) for current guidelines. Initially, PEGylated
interferon combined with oral ribavirin provided about 50% sustained virologic response
(SVR) or “cure” rate. Direct-acting antivirals (DAAs) are now the preferred treatment and
include oral agents: elbasvir/grazoprevir, ledipasvir/sofosbuvir, simeprevir/sofosbuvir, and
sofosbuvir/velpatasvir.
Treatment is often based on genotype, viral load, presence/absence of cirrhosis,
previous treatment failures, and insurance formularies. New drugs are constantly
entering the development pipeline, and many patients may be offered enrollment
in clinical trials. All patients with chronic hepatitis C should be vaccinated against
hepatitis A virus and hepatitis B virus to prevent additional liver disease from these
infections.
8
CHAPTER 4 HEPATITIS C
Hepatitis C
Simplified Testing Algorithm
HCV Risk Factors
ALT
HCV Ab
6 Main
Genotypes
HCV Viral Load Quant Consider 1–6
HCV Genotype Repeating in
3-6 Months
= 2% Vertical Transmission
Blood Clotting
Transfusion Factors
< July 1992 < 1987
Intranasal
Cocaine
1992
Genotype 2
Genotype 3
10%
10%
type
Geno
4,5,6
Genotype 1
75%
1a 60%
1b 15%
Genotype
9
PART 1 VIRAL HEPATITIS
Geographic Regions Affected: Worldwide; Higher incidences where hepatitis B is endemic. Hepatitis D is rare in
the United States.
Description: Hepatitis D is a “defective” single-stranded RNA virus that requires the machinery
and assistance of hepatitis B to replicate. HDV is acquired as either a coinfection
(simultaneously acquired with hepatitis B) or as a superinfection (acquired by a
person who already has chronic hepatitis B).
Signs and Symptoms: When acquired as a coinfection, HDV can increase the likelihood of severe illness and
fulminant hepatic failure. Coinfections are less likely to result in chronic hepatitis D.
Superinfections are more likely to cause chronic hepatitis D and can worsen preexisting
liver disease.
Diagnostic Testing: Since patients cannot have hepatitis D without hepatitis B, patients will test positive
for hepatitis B serum markers. IgM and IgG anti-HDV antibody testing is available
in the United States, and an elevated anti-HDV IgG titer can be seen in chronic
hepatitis D infections. Patients testing positive for HDV antibodies can be followed
up with HDV viral levels via PCR technology.
Pearls: HDV infections cannot exist without hepatitis B. The incubation period for
hepatitis D coinfection is identical to that of acute hepatitis B (the HDV infection
occurs concurrently with HBV). The presence of HBsAg and IgM anti-HBc is
essential for the diagnosis of HDV infections.
10
CHAPTER 5 HEPATITIS D
Hepatitis D
Co-infection occurs
when Hep B + D
arrive simultaneously.
It’s indistinguishable
from acute Hep B.
Super-infection occurs
when D is introduced into a
chronic HBsAg carrier and
presents as severe acute
hepatitis or exacerbation of a
chronic hepatitis.
Miss B, may I
super-infect you
with D?
11
PART 1 VIRAL HEPATITIS
Geographic Regions Affected: Central America, Africa, Middle East, India, and Asia
Description: HEV is a fecal-oral (genotype 1 and 2) and foodborne (genotype 3 and 4) single-stranded
RNA virus responsible for acute viral hepatitis. There are four major viral genotypes,
each associated with specific regions and unique clinical presentations. Genotype 3
is found in developed countries, tends to affect those patients .40 years old or
immunocompromised, and can cause chronic infections. Genotypes 1, 2, and
4 more commonly affect younger adults. HEV infections can occur as sporadic
outbreaks affecting many people or as isolated cases affecting isolated individuals.
Signs and Symptoms: Most cases are asymptomatic, with fewer than 5% of patients showing signs of acute
infection. When symptomatic, patients may exhibit malaise, fever, nausea, vomiting,
abdominal pain, arthralgia, and jaundice. Fulminant hepatic failure can occur in up
to 3% of infections and is more common in pregnant females and in those with
preexisting liver disease.
Diagnostic Testing: There are no commercially approved tests for HEV in the United States. Some
countries have access to IgM, IgG, and HEV PCR testing capabilities. Acute
infection would be determined by a positive IgM and HEV PCR viral load. IgM
is elevated in the acute setting and indicates recent exposure to the HEV virus,
whereas IgG increases during convalescence and confirms past exposure. In
chronic HEV infections, HEV RNA will be detectable via PCR in serum or stool
more than 6 months after initial infection.
Treatments: Supportive. Ribavirin may be beneficial in the treatment of chronic HEV infection.
There is an HEV vaccine that is licensed in China.
Pearls: Acute hepatitis E infection during pregnancy has a high mortality rate (up to 25%).
12
CHAPTER 6 HEPATITIS E
Hepatitis E
NA Virus
ssR
4G
enot ypes
25%
Mortality
13
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PART 2
INFECTIOUS
DIARRHEA
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1
PART 2
Section
BACTERIAL
PART 2 INFECTIOUS DIARRHEA
Causative Agent: Four serogroups of Shigella, broken down into group A: S. dysenteriae; group B:
S. flexneri; group C: S. boydii; and group D: S. sonnei.
Transmission: Transmission is fecal-oral. Because a very small inoculum of bacteria (10–100 organisms)
is required for transmission, infected food handlers can easily spread the disease.
Person-to-person transmission is common. Consumption of contaminated water,
food, or produce grown where sewage is used as fertilizer often results in illness.
Given the low inoculum required for transmission, there can be rapid spread in
closed quarters such as military campaigns, refugee camps, day care centers, and
households.
Description: An acute bacterial hemorrhagic diarrheal illness caused by any one of four Shigella
serogroups. Key symptoms include bloody diarrhea, abdominal pain, and fever.
Severe dehydration is uncommon.
Signs and Symptoms: Diarrhea, fever, abdominal pain and cramps, tenesmus, malaise, nausea, and
vomiting. Diarrhea is initially watery and nonbloody then becomes mucoid and
bloody as the infection transitions into the large bowel. Symptoms typically last
5–7 days without treatment. Complications can include hemolytic uremic
syndrome (HUS), seizures in children, and reactive arthritis.
Diagnostic Testing: Shigella should be suspected in patients presenting with bloody diarrhea, abdominal
pain, fever, and small, frequent stool volumes. Stool can be cultured or tested using
PCR.
Treatments: Antibiotics can reduce the duration of symptoms in infected patients. Because
antibiotic resistance to TMP/SMX and ampicillin is commonplace, current
recommendations call for either azithromycin or ciprofloxacin. However, providers
should be aware of emerging resistance to these antibiotics as well. Antispasmodics
should be avoided.
Pearls: Shigella is the most infectious bacterial diarrheal disease, commonly passed via
person-to-person transmission. S. dysenteriae serotype 1 (formerly Shigella shigae)
tends to be a more aggressive pathogen, whereas S. sonnei tends to cause milder
disease. S. sonnei is more common in developed nations, and S. flexneri is more
common in less-developed nations.
18
CHAPTER 7 SHIGELLOSIS
Shigellosis
Shigella
BACTERIAL
(Bacillary Dysentery) 4 Serogroups
A: S. dysenteriae
B: S. flexneri
C: S. boydii
D: S. sonnei
Incubation: 1-7 Days
Average: 3 Gram Rod
Diarrhea: 5-7 Days
Military Street meats!
Campaigns Handmade,
hand served!
Fever
Nausea Food
Vomiting
19
PART 2 INFECTIOUS DIARRHEA
Description: An acute, febrile, bacterial diarrheal illness often transmitted by undercooked poultry
(chicken/raw eggs) and characterized by watery and/or bloody diarrhea.
Signs and Symptoms: Typical symptoms include fever, malaise, nausea, vomiting, abdominal pain/cramps,
tenesmus, and diarrhea. Bloody diarrhea can also occur and is more common in
children. The illness is often self-limiting, and symptoms typically resolve within
3–7 days. More severe infections are seen with larger bacterial inoculums, in young
children and older adults, and the immunocompromised. Salmonella may become
invasive and can cause bacteremia, meningitis, septic arthritis, and osteomyelitis (sickle
cell patients are at increased risk). Postinfectious irritable bowel syndrome and reactive
arthritis may occur in some patients.
Treatments: The mainstay of treatment is often supportive and consists of fluids and a gentle diet.
Antibiotics are indicated in cases of severe illness, persistent fever, high-risk patients
(extremes of age, weakened immune systems), and those with invasive disease.
Treatment options may include fluoroquinolones (ciprofloxacin or levofloxacin),
macrolides (azithromycin), or cephalosporins (ceftriaxone or cefotaxime). Resistance
to TMP/SMX and other antibiotics is on the rise.
Pearls: The Food and Drug Administration has banned the sale of pet turtles less than 4 inches
in length since 1975 to reduce the incidence of salmonellosis in children. The Centers
for Disease Control and Prevention estimates that 100,000 cases of the disease have been
prevented as a result of this ban.
20
CHAPTER 8 SALMONELLOSIS
Salmonellosis
BACTERIAL
(Non-typhoidal Salmonella)
Salmonella
2 species High Risk:
Incubation:
S. bongori
12-48 Hours
S. enterica
Diarrhea: 3-7 Days
Gram rod
Sickle Cell =
Fever Osteomyelitis
Nausea
Vomiting
Non-typhoidal Salmonella
Abdominal (NTS)
Pain/Cramps
Tenesmus Reactive Arthritis
S. bongori
Diarrhea: Watery/Bloody
1994
2008
21
PART 2 INFECTIOUS DIARRHEA
Geographic Regions Affected: Resource-poor countries, mostly in Africa, Asia, the Caribbean, and Central and
South America. Peaks are seen before and after rainy seasons.
Description: An acute, afebrile, painless, bacterial diarrheal illness characterized by profound fluid
loss and the passage of “rice water stools.” Severe cases can cause severe electrolyte
abnormalities, renal failure, acidosis, hypovolemic shock, circulatory collapse, and
death.
Signs and Symptoms: Cholera is a spectrum disease with diarrheal symptoms ranging from asymptomatic
or mild to severe. Severe illness causes hypovolemic shock and death. After a brief
incubation period, patients develop nausea, vomiting, painless diarrhea, and lethargy.
Fever is uncommon. Diarrhea is nonbloody, may contain flecks of mucus (rice water
stools), and has a fishy odor. Volume losses of 10–20 liters per day can occur in
adults, resulting in hypovolemic shock, sunken eyes, and loss of skin turgor and
elasticity (washerwoman hands). Severe acidosis secondary to bicarbonate loss can
trigger Kussmaul respirations.
Diagnostic Testing: Clinical signs and symptoms, specifically in the setting of an outbreak of watery
diarrhea, should raise suspicions to the diagnosis. Darkfield microscopy may show
motile Vibrio bacteria. Rapid diagnostic tests can identify the O1 and/or O139
antigens in stool samples. Labs from severely ill patients will reflect the electrolyte,
pH, and renal abnormalities associated with severe dehydration and acidosis.
Ultimately, a positive stool culture is considered the gold standard for diagnosis.
Treatments: The mainstay of treatment consists of IV fluid resuscitation with lactated Ringer’s
solution followed by transition to oral rehydration salts once tolerated. Antibiotics can
shorten the duration of illness in severe disease and include doxycycline, azithromycin,
tetracycline, or erythromycin. Vaccines are available in endemic areas of the world
and for those U.S. travelers headed to endemic regions (relief workers, extended
medical missions, etc.).
Pearls: There was a significant outbreak of cholera in Haiti after a major earthquake in
2010. Patients with blood group O may have worse disease. Cholera epidemics are
associated with O1 and O139 serogroups; O139 is only found in Asia.
22
CHAPTER 9 CHOLERA
Cholera ibr
io cholera
BACTERIAL
V
e
(Blue Death) Rice
Water
Incubation: Gr
am Rod
1-5 Days
Diarrhea: 4-6 Days
Severe Cholera = Peaks before and
Shock w/i 24 Hours after rainy seasons
Lethargy
Sunken Eyes
Fever
Massive IVF Uncommon
Washerwoman Hands
Nausea (Very Thin Fingers)
Vomiting
Hypotension
Kussmaul
Respirations
Oral Rehydration
Painless Diarrhea Cholera Toxin
(CT)
Rice Water
Fishy Odor
Stools
V. cholerae O1
Epidemics
V. cholerae O139
23
PART 2 INFECTIOUS DIARRHEA
Reservoir: Gastrointestinal tract of animals and livestock; poultry is the most common. Domestic
dogs and cats may also be colonized.
Description: An acute, febrile, bacterial diarrheal illness characterized by watery diarrhea that
frequently becomes bloody after a few days.
Signs and Symptoms: Patients may have a febrile prodrome before the diarrhea occurs. Typical symptoms
include fever, malaise, abdominal pain/cramps, tenesmus, and watery diarrhea that
often becomes bloody. Nausea and vomiting may occur in some patients. The illness
is often self-limiting and symptoms typically resolve within 7 days. In the acute
setting, some patients may develop right lower quadrant abdominal pain prior to
the onset of diarrhea (pseudoappendicitis). Postinfectious complications can include
Guillain-Barré syndrome and reactive arthritis.
Diagnostic Testing: Stool culture is the gold standard for diagnosis. Darkfield or phase-contrast microscopy
may reveal the motile, gram-negative, curved/helical-shaped rods. There are some stool
antigen and PCR tests available as well.
Treatments: The mainstay of treatment is often supportive and consists of fluids and a gentle diet.
Antibiotics will decrease the duration of illness and options include azithromycin
500 mg daily 3 3 days or erythromycin 500 mg four times daily 3 5 days. There is
worldwide emerging campylobacter resistance to fluoroquinolones, specifically in
Southeast Asia.
24
CHAPTER 10 CAMPYLOBACTERIOSIS
Campylobacteriosis
BACTERIAL
lobacter
py lobact je
py e
Cam
ju coli
ni
r
Cam
Incubation: 1-7 Days
Gra m
Average: 3 Days
Rod
Diarrhea 7 Days e
d
He
lical-shap
C. jejuni is in my guts
and I don’t get sick!
Cook me!
Fever
Nausea
Vomiting
Guillain-Barré
Syndrome
Tenesmus
Reactive Arthritis
Watery/Bloody
Diarrhea
Pseudoappendicitis
25
PART 2 INFECTIOUS DIARRHEA
Causative Agent: Escherichia coli bacteria strains capable of producing Shiga toxin, known as “Shiga
toxin–producing E. coli” (STEC). Strains identified in significant outbreaks have
included E. coli O157:H7 (most common in North America, Jack in the Box in 1993),
O104:H4 (Germany and Europe in 2011), and O26 (Chipotle in 2015).
Reservoir: Ruminant animals: Cattle, goats, sheep, deer, and elk. Cattle are the main reservoir.
Description: An acute bacterial hemorrhagic diarrheal illness caused by STEC. Key symptoms
include bloody diarrhea, abdominal pain, cramps, leukocytosis, and absence of
fever.
Signs and Symptoms: Bloody diarrhea, abdominal pain, cramps, tenesmus, malaise, and anorexia. Fever
is notably absent. Symptoms typically resolve over 5–7 days without intervention.
Hemolytic uremic syndrome (HUS), a triad of hemolytic anemia, renal failure, and
thrombocytopenia, occurs in 5%–10% of cases. HUS is more common in children
under 10 years old (affecting about 15%) and those treated with antibiotics (up to
25% of children). HUS typically occurs 5–10 days after the onset of diarrhea, just
as the diarrhea is becoming less frequent.
Diagnostic Testing: STEC should be suspected in patients presenting with bloody diarrhea, abdominal
pain, and absence of fever. Stool can be cultured using sorbitol-MacConkey agar.
Enzyme-linked immunosorbent assays for Shiga toxin 1 and 2. PCR for Shiga toxin
gene, anti-LPS (anti-lipopolysaccharide) IgM and IgG antibodies can also be obtained.
Pearls: There have been several infamous outbreaks of STEC in the United States associated
with fast food restaurants, including Jack in the Box in 1993 and Chipotle in 2015.
26
CHAPTER 11 ENTEROHEMORRHAGIC ESCHERICHIA COLI
Enterotohemorrhagic E. coli
BACTERIAL
(EHEC)
erichia c
ch
ol
Es
i
Incubation: 3-8 Days
Average: 3-4 Days
Diarrhea: 5-7 Days Gr
am Ro
d
1993
Abdominal Pain/Cramps
Shiga Toxin 1&2
O157:H7
Tenesmus O104:H4
O26
Anorexia
ABX HUS
in Children
27
PART 2 INFECTIOUS DIARRHEA
Causative Agent: Escherichia coli bacteria strains capable of producing one of two toxins: heat-stable
(ST) enterotoxin, which increases intracellular cGMP, and heat-labile (LT) enterotoxin,
which increases intracellular cAMP. These toxins stimulate the intestines to increase
fluid secretion, causing non-bloody diarrhea. Enterotoxigenic Escherichia coli (ETEC)
bacteria may produce either or both toxins.
Description: An acute, profuse watery diarrheal illness caused by ST or LT toxin producing strains
of E. coli (ETEC) bacteria. Key symptoms include watery diarrhea, abdominal pain,
cramps, malaise, anorexia, and absence of fever.
Signs and Symptoms: Profuse watery diarrhea, abdominal pain and cramps, tenesmus, malaise, and
anorexia. Fever is notably absent. Symptoms typically resolve over 3–4 days without
intervention.
Diagnostic Testing: ETEC or “traveler’s diarrhea” is often diagnosed based on patient’s symptoms and
history of recent travel. Often, by the time the patient comes to a healthcare provider’s
attention, symptoms have begun to resolve. Since both bacterial and viral causes of
“traveler’s diarrhea” have very short incubation periods, giardia or other parasites
should strongly be considered in those patients who develop diarrhea 1–2 weeks
after returning from travel.
Treatments: The mainstay of treatment is supportive and consists of fluids and a gentle diet.
Handwashing, drinking bottled water, and avoiding street meats/street vendors, iced
drinks, salads (uncooked vegetables), and fruits may reduce risk of transmission.
Bismuth subsalicylate taken prophylactically may reduce likelihood of infection.
Azithromycin 1000 mg as a single dose or 500 mg daily 3 3 days, ciprofloxacin
750 mg twice daily for 1–3 days, or levofloxacin 500 mg daily for 1–3 days can be
prescribed to travelers to take if they develop diarrhea while abroad. Since the actual
cause of “traveler’s diarrhea” cannot be determined in the field, while the traveler is
abroad, azithromycin is the preferred antibiotic—it covers campylobacter, a bacterium
with emerging resistance to fluoroquinolones, specifically in Southeast Asia.
28
CHAPTER 12 ENTEROTOXIGENIC ESCHERICHIA COLI
Enterotoxigenic E. coli
BACTERIAL
(ETEC/Traveler’s Diarrhea/Montezuma’s Revenge)
erichia c
ch
ol
Es
i
Incubation: 8-72 Hours
Diarrhea: 3-4 Days Gr
am Ro
d
Fever Uncommon
Malaise
Heat-Stable
Abdominal Pain/Cramps Enterotoxin (ST)
Activates cGMP
Heat-Labile
Enterotoxin (LT)
Tenesmus Activates cAMP
Watery Diarrhea
Contaminated Water Anorexia
Non-bloody
29
PART 2 INFECTIOUS DIARRHEA
Reservoir: Pigs, rodents, rabbits, sheep, horses, dogs, and cats. Pigs are the most important.
Description: Yersiniosis may have a variety of presentations. Y. enterocolitica often causes an acute,
febrile, bacterial diarrheal illness characterized by nausea, vomiting, abdominal pain,
and bloody diarrhea. Y. pseudotuberculosis often presents as pseudoappendicitis,
occasionally without diarrhea.
Signs and Symptoms: Infants and children often have worse disease than adults. Infants may develop
necrotizing enterocolitis. Typical symptoms in children and adults include fever,
malaise, abdominal pain, cramps, tenesmus, nausea, vomiting, and bloody diarrhea.
The illness is often self-limiting, and symptoms typically resolve within 1–3 weeks.
Y. enterocolitica may present as pharyngitis without diarrhea. Some patients may
develop right lower quadrant abdominal pain secondary to mesenteric lymphadenitis
and present as pseudoappendicitis. Bacteremia and hematogenous spread can occur
and is more common in infants and the immunocompromised. Postinfectious
complications include erythema nodosum and reactive arthritis.
Diagnostic Testing: Culture from the source of infection (stool, pharynx, blood, etc.) is the gold standard
for diagnosis. Serologic testing is used in Europe and Japan, but it is not widely
available in the U.S.
Treatments: For diarrheal illness, the mainstay of treatment is often supportive and consists of
fluids. Antibiotics are indicated for severe infections and include doxycycline
combined with an aminoglycoside, TMP/SMX, or fluoroquinolones.
Pearls: Hemochromatosis and iron overload states predispose patients to yersinia infections.
Desferrioxamine therapy increases disease severity and should be discontinued in
infected patients.
30
CHAPTER 13 YERSINIOSIS
Yersiniosis
BACTERIAL
Yersinia enterocolitica
Yersinia pseudotuberculosis
Incubation: 1–14 Days
Average: 4–6 Days
Diarrhea: 1–3 Weeks
Gram Rod
Nausea
Vomiting Diarrhea can be
absent in
Y. pseudotuberculosis
Abdominal Pain/ Reactive
Cramps Arthritis
Tenesmus
Watery/Bloody
Symptoms in Infants
Diarrhea
& Children > Adults
Pseudoappendicitis
31
PART 2 INFECTIOUS DIARRHEA
Incubation: Varied
Description: Clostridium difficile is a gram-positive spore and toxin-forming bacteria that can
colonize the human gastrointestinal tract and causes antibiotic-associated diarrhea.
The infection is a spectrum disorder, with symptoms ranging from asymptomatic
colonization to severe colitis. The disease is more common in elderly patients and is
associated with antibiotic use. Antibiotics decrease normal colonic flora and can
allow for C. diff overgrowth and symptom manifestation. The antibiotics most
associated with C. diff include clindamycin, fluoroquinolones, and second-generation
(and above) cephalosporins.
Signs and Symptoms: Watery diarrhea beginning during or after recent antibiotic use is the classic disease
manifestation. Other symptoms include fever, malaise, abdominal pain, cramps, and
tenesmus. Severe disease can cause profound dehydration, hypotension, shock, acidosis,
abdominal distension, and toxic megacolon (which may lead to perforation).
Diagnostic Testing: Leukocytosis is common. Leukocytosis, elevated creatinine, decreased albumin, and
elevated lactate are markers for disease severity. Fecal leukocytes will be positive.
Stool can be cultured and/or sent for PCR analysis and/or EIA testing for Toxin A
and B. Since only Toxin B is associated with diarrheal illness, PCR and EIA testing
may be limited to that toxin in some institutions.
Treatments: Discontinue the offending antibiotics if possible. Treatment of C. diff can be with oral
metronidazole, vancomycin, or fidaxomicin. Severe disease requires intravenous (IV)
metronidazole. IV vancomycin is not effective for C. diff. Fecal microbial transplant
is being investigated as another treatment option.
Pearls: Proton-pump inhibitors (PPIs) and H2 acid blockers are associated with increased
risk of C. diff. If colonoscopy is performed, mucosal friability, edema, inflammation,
and pseudomembranes will be visualized. Only liquid stool is sent for culture/PCR
testing, as diarrhea with solid/semi-solid stool is not consistent with C. diff infection.
32
CHAPTER 14 CLOSTRIDIUM DIFFICILE INFECTION
BACTERIAL
(Pseudomembranous Colitis)
idiu m diffi
str c
Clo
ile
Spore-Forming
WBC
Creatinine = BAD
Albumin Gr
am + Rods
+
Clindamycin
Fluoroquinolones = Worst Offenders
Pseudomembrane 2nd-Gen + Cephalosporins
Fever
Stop the offending
antibiotics!
>6 cm
Toxic Megacolon Perforation
Risk
Abdominal Pain/
Cramps Diarrhea +
Recent ABX Use = C. diff
Fecal Tenesmus
Transplant >3 Watery Stools <24 Hrs.
Toxin A Toxin B
PCR
Stool Culture
Fecal Leukocytes
33
PART 2 INFECTIOUS DIARRHEA
Description: Vibrio bacteria are common to marine and brackish waters (estuaries, saltwater
marshlands), and shellfish living in these waters concentrate the bacteria, making
vibrio a common cause of shellfish-associated diarrhea. Since bacterial concentration
increases as water temperatures rise, highest disease incidence is noted in the United
States between April and September. In addition to causing gastrointestinal illness,
vibrio can also cause significant wound infections and/or septicemia. Vibrio
infection tends to be worse in the immunocompromised, those with chronic
liver disease, and alcoholics.
Signs and Symptoms: Gastroenteritis: Vibriosis should be suspected when watery diarrhea begins shortly
after recent raw or undercooked shellfish consumption (oysters and clams are most
common). Other symptoms include abdominal pain, cramps, nausea, and vomiting.
Diarrhea may become bloody. Soft Tissue Infection: Wound exposure to vibrio can
occur if cut while swimming in marine or brackish waters or when handling infected
shellfish. In severe cases, cellulitis can expand rapidly, cause hemorrhagic bullae and/or
necrotizing fasciitis. Septicemia: High-risk patients exposed to vibrio may develop
bacteremia and sepsis after consumption of infected shellfish or secondary from a
wound infection. Shock rapidly follows the onset of sepsis and patients have an
extremely high mortality. This pathologic process is most common in those with
compromised immune systems and/or chronic liver disease.
Treatments: Gastroenteritis: Mild to moderate disease can be treated with intravenous or oral
hydration. Antibiotics may shorten the duration of illness in more-severe cases. Soft
Tissue Infections and/or Septicemia: Doxycycline or minocycline 100 mg twice daily
1 ceftriaxone 2 grams IV daily is the suggested regimen for severe infections.
Intravenous cefotaxime 1 ciprofloxacin and fluoroquinolone monotherapy are
alternatives. Aggressive treatment is necessary in soft tissue infections and sepsis.
Pearls: While either species can present in any of the above scenarios, V. parahaemolyticus is
more commonly associated with gastroenteritis and V. vulnificus is more commonly
implicated in severe soft tissue infections and septicemia. Most restaurant menus
warn consumers with chronic liver disease and/or immunodeficiency to avoid raw
shellfish for this reason.
34
CHAPTER 15 VIBRIOSIS
Vibriosis
h a e m ol y
aravulnificu ti
BACTERIAL
.
V. p
cu
V
s
s
Incubation: 24–72 Hours
Peak: April–October Gra s
m Rod
Gastroenteritis
Nausea/Vomiting Septicemia
Diarrhea
Abdominal Pain/Cramps High Fever/Chills
Soft Tissue High Mortality
Infections
Cellutitis Rapid Progression
Hemorrhagic Bullae
Chronic Liver Disease =
Worse Infections
Diarrhea
(Potentally Bloody)
Cellulitis with
Hemorrhagic Bullae
35
2
PART 2
Section
VIRAL
PART 2 INFECTIOUS DIARRHEA
Transmission: Fecal-oral transition, typically spread via contact with contaminated surfaces, the
consumption of contaminated food or water, or aerosolized virus from vomitus. The
virus can live outside the body for long periods of time and can be shed for weeks
after symptoms have resolved.
Description: Norovirus is an extremely contagious virus responsible for up to 1/5 of all cases of
gastroenteritis worldwide. It is known for causing outbreaks on cruise ships and in
daycare centers, nursing homes, and schools.
Signs and Symptoms: Norovirus infections typically present acutely with generalized malaise, headache,
myalgia, nausea, vomiting, watery diarrhea, abdominal cramping, and low-grade
fever. The disease is self-limiting, and symptoms tend to resolve over 1–3 days.
VIRAL
Diagnostic Testing: Norovirus infections are often diagnosed based on clinical presentation alone. PCR
testing of stool samples is not routinely done or recommended since asymptomatic
shedding is common. However, if PCR testing is pursued, stool samples should be
obtained within 48–72 hours of symptom onset.
Treatments: Supportive.
Pearls: The Centers for Disease Control (CDC) investigates and tracks outbreaks of
gastroenteritis on cruise ships, and, not surprisingly, most are caused by NoV.
38
CHAPTER 16 NOROVIRUS
Norovirus
o rovirus NoV
(Norwalk Virus) N
(Winter Vomiting Bug)
(Stomach Flu)
ig
s!
u
H
hly
Incubation: 12–48 Hours I nfec tio
Diarrhea: 1–3 Days
Most Common
in Winter
Outbreaks on
Cruise Ship! Generalized
Malaise Mild
Headache
Anchors Aerosolized Virus
from the Vomit
Aweigh!
VIRAL
Low-Grade
Fever
Nausea
Vomiting
Abdominal
Cramping
Watery
Diarrhea
Fecal-Oral
39
PART 2 INFECTIOUS DIARRHEA
Transmission: Fecal-oral transmission, typically spread via contact with contaminated surfaces, the
consumption of contaminated food or water, or aerosolized virus. The virus can live
outside the body in water for several days.
Geographic Regions Affected: Worldwide. Greater morbidity and mortality is noted in less-developed nations.
Description: Rotavirus causes viral gastroenteritis and is the common cause of diarrhea in infants
and young children.
Signs and Symptoms: Rotavirus is a spectrum diarrheal illness, with symptoms ranging from mild to
severe. The disease has the most profound impact on children 6–24 months old and
rarely affects adults. Symptoms include malaise, nausea, vomiting, watery diarrhea,
and low-grade fever. With significant fluid loss, severe dehydration and even death
can occur. Signs of dehydration in infants include decreased tears, decreased urine
output, decreased skin turgor, and irritability or lassitude. When profound dehydration
is not an issue, the disease is self-limiting, and symptoms tend to resolve over 4–8 days.
VIRAL
Most people have been infected by rotavirus at least once before the age of 5 years.
Reinfection can occur throughout life; subsequent illnesses are less severe.
Diagnostic Testing: Diagnosis is often based on clinical suspicion. ELISA testing can be used to detect
viral antigens in stool samples. PCR can also be performed on stool samples and is
the most sensitive technique for rotavirus detection.
Treatments: Supportive. There are two licensed vaccines available in the United States.
Pearls: After the introduction of safe and effective vaccines, the number and severity of cases
and subsequent hospitalizations in the United States and other developed nations has
trended down dramatically. Diarrheal illness is still a leading cause of death in children
under the age of 5 worldwide.
40
CHAPTER 17 ROTAVIRUS
Rotavirus tavirus
Ro
dsR
e
NA
da
Diarrhea: 4–8 Days ri
Reovi
6 m–2 y/o Most
Severe Symptoms
Severe Dehydration
Nausea
VIRAL
Vomiting Low-
Grade
Fever
Stool ELISA
Stool PCR
41
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3
PART 2
Section
PROTOZOAN
PART 2 INFECTIOUS DIARRHEA
Geographic Regions Affected: Worldwide—It is the number 1 intestinal parasite disease in the United States.
Description: Giardia is a flagellated intestinal protozoan responsible for acute and chronic outbreaks
of gastrointestinal (GI) and diarrheal illnesses worldwide. It is contracted via the
ingestion of infectious cysts through the fecal-oral route, often from consuming
contaminated food or water.
Signs and Symptoms: The disease may be asymptomatic, acute and self-limiting, or chronic. Acutely,
patients may have abdominal pain and cramping, malaise, upper GI upset, and
diarrhea. The diarrhea is often described as green, frothy, foul smelling, and often
floats, indicating malabsorption. Chronically, patients may develop anorexia, weight
loss, malabsorption, B12 deficiency, postinfectious irritable bowel syndrome, and
lactose intolerance.
Diagnostic Testing: Ovum and parasite stool studies 33 can be obtained. Stool antigen and nucleic acid
amplification testing (NAAT) are also available.
Treatments: Tinidazole 2 grams by mouth once, nitazoxanide 500 mg twice a day 3 3 days, or
metronidazole 250 mg three times a day 3 5 days.
Prevention: Proper sanitation and handwashing limits spread. Water can be boiled, filtered, or
halogenated (chlorine or iodine) to eliminate and/or decrease the number of cysts.
Pearls: The disease is more common in children and middle-aged adults. Backpackers,
campers, international travelers, people in child care centers, and men who have sex
with men (MSM) are at higher risk of acquiring giardiasis. Giardia, given its incubation
period, delayed onset, and potential for chronicity, should be considered in the
returned traveler presenting with diarrheal illness. This is in contrast to acute-onset
“traveler’s diarrhea,” which is often self-limiting and bacterial or viral in nature.
PROTOZOAN
44
CHAPTER 18 GIARDIASIS
Giardiasis
ia lamb
ard li
(Beaver Fever) Gi
a
Anaero
zoa
oto
ic
Pr
b
Fl a g d
Incubation: 1–3 Weeks ellate
Diarrhea: 2–6 Weeks
Burping
Abdominal
Bloating
NAAT,
Stool Antigen,
or O&P PROTOZOAN
Fecal-Oral Green, Frothy,
Foul-Smelling
Diarrhea
3 Stool Samples
45
PART 2 INFECTIOUS DIARRHEA
Signs and Symptoms: Symptoms of intestinal disease include malaise, fatigue, low-grade fever, abdominal
pain, cramps, and watery diarrhea. Diarrhea in immunocompetent patients often
resolves within 2 weeks. Immunocompromised (HIV/AIDS) patients have more
significant disease and biliary tree involvement (cholecystitis, cholangitis) and are more
likely to have chronic diarrhea and associated weight loss. Respiratory cryptosporidiosis
can occur, is rare, and is more common in immunocompromised patients.
Diagnostic Testing: Up to three stool samples may be required to make the diagnosis via microscopy.
PCR is the diagnostic method of choice. Serologic antigen tests are also available.
Treatments: Oral nitazoxanide 500 mg twice a day orally for 3 days is effective for immunocompetent
patients. For those with HIV/AIDS, the best means of treatment is to maximize the
HAART antiretroviral therapy.
Pearls: Exposure to fecal matter, such as work in child care centers or sexual activity, increases
risk of infection. Outbreaks in community pools are not uncommon in the United
States and have been linked to infants swimming while wearing diapers.
PROTOZOAN
46
CHAPTER 19 CRYPTOSPORIDIOSIS
Cryptosporidiosis oridium
t osp idium par v
(Crypto) yp spo r ho
um in i s
o
Cr y Cr
m
pt
Incubation: 2–28 Days
5–10 Days Average
Diarrhea: 2 Weeks
Pro tozo a
HIV/AIDS = Worse
Malaise/Fatigue
Associated with Intestinal Variant
Low-
Grade
Fever
Upper Respiratory
Rhinorrhea
Hoarseness
Watery
Diarrhea
Can be:
PROTOZOAN
Fecal-Oral
Chlorine Resistant
PCR,
Antigen Stool
Test, or O&P
3 Stool Samples
47
PART 2 INFECTIOUS DIARRHEA
Transmission: Fecal-oral transmission of infectious cysts. Cysts can survive outside the human body
for weeks to months and are transmitted via person-to-person contact or the ingestion
of contaminated food or water. Once ingested, cysts mature into trophozoites and
typically invade the colonic mucosa.
Geographic Regions Affected: Worldwide, more common in tropics and developing nations with poor sanitation.
Description: Amebiasis is a spectrum diarrheal illness ranging from asymptomatic carrier states to
hemorrhagic colitis and dysentery. Hematogenous spread may cause extraintestinal
disease.
Signs and Symptoms: Symptom onset tends to be gradual and includes fever, malaise, abdominal pain,
weight loss, and bloody diarrhea. These invasive amebas can cause characteristic
flask-shaped ulcers in the colonic mucosa and rarely, large granulomatous masses
(amebomas) resembling cancerous tumors may form. Toxic megacolon and
perforation are potential complications of severe acute disease. There is also a
potential for invasive, extraintestinal disease secondary to hematogenous spread
to the liver, brain, or lungs. Amebic liver abscesses are the most common
extraintestinal manifestation and cause fever, chills, weight loss, and right upper
quadrant pain. Abscesses may enlarge to the point of rupture.
Diagnostic Testing: Microscopy may identify cysts and/or trophozoites of amebas, but it cannot differentiate
between pathologic and nonpathologic species. Stool antigen and PCR testing
confirm the diagnosis. Serology is helpful in the diagnosis of amebic liver abscess
and extraintestinal disease. Imaging for liver abscess includes CT, US, and/or MRI.
Abscesses may be aspirated by interventional radiology and sent for microscopy,
antigen, and/or PRC testing.
Treatments: Asymptomatic patients should be treated to prevent disease progression and transmission
to others. Luminal agents, such as paromomycin, iodoquinol, and diloxanide, are poorly
absorbed from the GI tract and are effective at cyst eradication. Mild to moderate
disease can be treated with oral metronidazole or tinidazole, followed by paromomycin
or iodoquinol to kill luminal-dwelling cysts. More-severe diarrheal disease and
extraintestinal disease should be treated with intravenous metronidazole or tinidazole
PROTOZOAN
48
CHAPTER 20 AMEBIASIS
Amebiasis
Ameba
En
a
tic
mo ly
ta
Incubation: 2–4 Weeks eba histo
Hematogenous Spread
to Brain/Lungs (Rare)
Flask-shaped
Ulcers
Granulomatous Mass
(Ameboma)
PROTOZOAN
10% Cases are
Invasive
Dysentery
49
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PART 3
CHILDHOOD
ILLNESSES
PART 3 CHILDHOOD ILLNESSES
Signs and Symptoms: Following a 7- to 21-day incubation period, patients develop prodromal symptoms,
including high fever (up to 40°C), malaise, conjunctivitis, coryza (runny nose), and
cough. Koplik spots, small white to gray spots on the buccal mucosa opposite the lower
molars, are pathognomonic and may appear 2–3 days before the viral exanthem. Koplik
spots have been described as “grains of salt on a red background.” After 3–4 days
(range 1–7 days) of prodromal symptoms, patients enter the exanthem phase of the
disease, characterized by the development of a red, maculopapular rash that starts
at the head and proceeds in a cephalocaudal (head to toe) and outward progression.
The rash persists for up to 7 days and fades in the same order it appeared. As the
rash resolves, patients enter the recovery phase and may continue to have a mild
cough for 1–2 weeks. Complications of measles include diarrhea, otitis media,
pneumonia, encephalitis, seizures, and death. Infection with measles confirms
lifelong immunity.
Diagnostic Testing: Serum IgM and IgG levels can be checked. IgM will become elevated in the acute phase
of the illness and remain elevated for 1–2 months. Polymerase chain reaction can be
used to detect the MV in serum, urine, and oropharyngeal and nasopharyngeal
secretions.
Pearls: Koplik spots are a temporary viral enanthem and are pathognomonic for measles.
Fever is high grade and tends to last for about 4 days and occurs concurrently with
conjunctivitis, coryza, and cough. Subacute sclerosing panencephalitis is a rare and
fatal degenerative disease of the central nervous system that occurs in some patients
7–10 years after initial infection.
52
CHAPTER 21 MEASLES
Measles
asles Virus
(Rubeola) Me
MV
ssRNA
Incubation: 7–21 Days
Average: 10–14 Days Pa s
ra my xovi ru
4 Ds
3 Cs
RASH
Koplik Spots on
4 Ds Buccal Mucosa
(Four Days)
Pathognomonic
s p r e a ds f ro m head
Red
Maculopapular
Rash Early 2015 outbreak
at a Famous California
to feet
Theme Park!!
53
PART 3 CHILDHOOD ILLNESSES
Description: Mumps is a vaccine-preventable, viral illness known to cause parotitis. The virus
reproduces in the upper respiratory tract and is spread via saliva, oropharyngeal
secretions, and respiratory droplets. Patients with mumps are considered contagious
and should be isolated, with droplet precautions for at least 5 days after the onset of
parotitis.
Signs and Symptoms: After a 12- to 25-day incubation period, patients develop prodromal symptoms,
including low-grade fever, headache, malaise, fatigue, and myalgia, followed by
parotitis. Parotid swelling is often bilateral (75%) and progresses over the next
72 hours. Glands remain swollen for about 1 week. While most cases of mumps are
self-limiting, complications, including orchitis, oophoritis (ovarian inflammation),
infertility, pancreatitis, meningitis, and/or deafness, can occur.
Diagnostic Testing: Diagnosis is often based on history and clinical presentation. Serology can reveal an
acute rise of IgM or a fourfold rise of IgG in the convalescence phase. IgG is of no
value in previously vaccinated patients. Serum and buccal/oral swabs can be tested
for mumps using PCR.
Treatments: Treatment is mostly supportive. Vaccination is the best way to prevent mumps.
54
CHAPTER 22 MUMPS
Mumps um
ps Vir
u
M
(Epidemic Parotitis)
s
RNA
ar
us
amyxovir
P
Incubation: 12–25 Days
Average: 16–18 Days
Peak: Winter–Spring
Headache
Malaise
Meningitis
Low-Grade
Fever
Pancreatitis
Orchitis
Ovarian Inflammation
Possible Infertility
55
PART 3 CHILDHOOD ILLNESSES
Signs and Symptoms: Many cases are asymptomatic, and children exhibit milder disease than adults.
Following a 12- to 23-day incubation period, patients develop a low-grade fever,
lymphadenopathy, and a mild maculopapular rash that proceeds in a cephalocaudal
(head to toe) and outward progression. Lymphadenopathy tends to affect the posterior
auricular, suboccipital, and posterior lymph nodes. Fever and lymphadenopathy may
precede the rash by a few days or occur concurrently. The rash is fainter than in
measles and lasts about 3 days; hence, the term “3-day measles.” Headache, malaise,
conjunctivitis, coryza, and cough may occur as part of the prodrome, more commonly
in older patients. Up to 70% of adolescents and adult females develop arthralgia and
arthritis that may persist for several months. Complications are more common in
older patients and may include thrombocytopenic purpura and encephalitis. Rubella
during pregnancy—specifically the first trimester—can cause stillbirth or birth defects.
Congenital rubella syndrome causes cataracts, heart defects, and deafness.
Diagnostic Testing: Serum IgM and IgG levels can be obtained. IgM will be elevated in the acute phase
of the illness, and a fourfold rise in IgG in convalescence will confirm recent infection.
PCR testing can be performed on oropharyngeal or nasopharyngeal swabs and urine.
Obtaining samples from both sources will increase the likelihood of detecting the
virus.
Pearls: Rubella and measles are similar but have some distinct differences. Rubella is
characterized by low-grade fever, lymphadenopathy, and rash. Measles is characterized
by high-grade fever, cough, coryza, conjunctivitis, and rash. The rash in rubella is
fainter (pink vs. red) and lasts for a shorter duration (3 days vs. 7 days). Rubella is a
milder disease but can cause congenital defects in pregnancy. Forchheimer spots are
transient erythematous petechiae seen as enanthem on the hard palate in about 20% of
patients with rubella. Since these spots can also be seen in measles and scarlet fever,
they are not pathognomonic for rubella. Koplik spots, however, small white to gray
spots on the buccal surface opposite the lower molars, are a pathognomonic
enanthem for measles.
56
CHAPTER 23 RUBELLA
57
PART 3 CHILDHOOD ILLNESSES
Peak Incidence: Late Winter—Early Spring. Peak incidence is in children 5–15 years old.
Description: Erythema infectiosum (EI) is a self-limiting febrile viral illness that produces a
characteristic “slapped cheek” facial rash followed by a lace-like reticular rash of the
trunk and extremities. Patients are most infectious prior to the development of the
rash.
Signs and Symptoms: After a 4- to 14-day incubation period, most patients experience a prodrome of
low-grade fever, malaise, headache, and rhinorrhea. After 2–5 days, a “slapped cheek”
facial rash develops followed 1–4 days later by a lacelike reticular rash on the trunk
and extremities. The rash can be pruritic, worsens with sunlight, and spares the
palms and soles. The rash typically lasts for 5–10 days and may periodically return
with exposure to sunlight, heat, exertion, or stress. Older children, adolescents, and
adults, particularly females, may develop a mild polyarthritis of the hands, wrists,
ankles, and knees that can last for several weeks or become chronic in some patients.
Diagnostic Testing: EI is typically diagnosed based on history and clinical presentation. IgM/IgG
serology and nucleic acid detection can be performed, but they should be
reserved for pregnant women with known exposure (risk of congenital defects)
and immunocompromised patients.
Treatments: Supportive. Ibuprofen or acetaminophen as needed for fever, myalgia, and arthralgia.
58
CHAPTER 24 ERYTHEMA INFECTIOSUM
Erythema Infectiosum
(Fifth Disease) ar v
ovirus B1
9
(Slap Face)
RASH
Headache
Rhinorrhea
Low-Grade
Fever
(Adolescents)
Mild Arthritis
59
PART 3 CHILDHOOD ILLNESSES
Causative Agent: Human Herpes Virus 6 (HHV 6) is the most frequent cause, but can also be caused
by Human Herpes Virus 7 (HHV 7), enteroviruses, or adenoviruses.
Peak Incidence: Occurs year round, mostly affecting children less than 2 years old.
Description: Exanthem subitum is an acute viral illness characterized by 3–5 days of high
fever followed by defervescence and the appearance of a blanching macular or
maculopapular centrifugal rash.
Signs and Symptoms: After an incubation period, children develop a high fever (up to 40°C) lasting for
3–5 days. During the febrile phase, children may have some irritability, malaise, and
anorexia; however, most children are unphased. Within 24 hours of defervescence a
blanching, nonpruritic, macular or maculopapular rash appears on the trunk and
later spreads to the face and extremities. The disease is self-limiting and results in
few complications. Occasionally, infants may experience febrile seizures.
60
CHAPTER 25 EXANTHEM SUBITUM
(Roseola)
ds
D N A V ir us
Incubation: 5–15 Days
3–5 Days
High Fever RASH
Fever Resolves
High
Fever
Centrifugal
Rash
61
PART 3 CHILDHOOD ILLNESSES
Signs and Symptoms: Primary infection occurs after an incubation period averaging 14–16 days. Initial
symptoms include a prodrome of fever and malaise (more common in adults)
1–2 days before the onset of a characteristic rash. The rash is pruritic and first
appears on the head, chest, and back before spreading to the extremities. Lesions
rapidly progress from macules and papules to vesicles before scabbing over. New
crops of lesions occur over the next 3–4 days, and most lesions crust over within a
week. Scabs remain for about 2 weeks before falling off. It is typical to have crops of
lesions at various stages; this is how the disease is diagnosed clinically. Chickenpox
tends to be a mild illness in young children and causes more severe presentations and
complications in adolescents, adults, and the immunocompromised. Complications
can include secondary bacterial skin infections, pneumonia, and encephalitis.
Pregnant women who develop chickenpox can pass the infection on to the fetus or
neonate, causing congenital varicella syndrome or neonatal varicella, respectively.
Diagnostic Testing: Chickenpox is often a clinical diagnosis. Polymerase chain reaction (PCR) testing of
blister fluid can be done in pregnant females to diagnose acute infections.
Treatments: Supportive. Calamine lotion can be applied to soothe the lesions and make them less
itchy. Acyclovir may have some benefit in the treatment of varicella pneumonia and
encephalitis. There are vaccines to prevent both primary infection (chickenpox) and
the reactivation of VZV (shingles).
Pearls: After a single dose of vaccine, some patients exposed to a wild strain of VZV may
develop a mild form of chickenpox referred to as “breakthrough disease.” These
patients will have a lower-grade fever, atypical rash pattern, and fewer lesions and
are less likely to develop complications. Although “breakthrough disease” could
potentially occur after the second dose of vaccine, it would be rare.
62
CHAPTER 26 CHICKENPOX
Chickenpox
a - zo ster
ell
Va r i c
Vir
us
Incubation: 10–21 Days dsDNA
Average: 14–16 Days VZ
V / H H V-3
Peak: Winter & Spring
Airborne
Airb Droplets
orne
Dise
ase
Blist
is Co
er Fl
u Descending
ntag id
ious Pattern
Rash
Ove rogreP
r 10– ss
12 H es
Not ours
Con
t
Only agiou
Scab s Onc
s Re e
main
Can
Cau
Pne se Var
Poss umonia icella
ible
Enc and
in A ephalit
dult is
s
In Pr
egn
Can a es
Ca nt Fem
Varic use Con ales Papul d
ella g es an
Synd enital
rom Vesicl s
e
Scab
Dew Drops on
Rose Petal
63
PART 3 CHILDHOOD ILLNESSES
C—Chickenpox: Varicella can be passed on to the child in utero, during the perinatal period, or just after
birth. In utero transmission, particularly early in pregnancy (,20 weeks), can cause
congenital varicella syndrome (CVS). This syndrome is characterized by one or more
abnormalities, including low birth weight, hypoplastic limbs, ocular defects, neurologic
defects (mental retardation, microcephaly, hydrocephalus), and/or cutaneous scars that
follow dermatomal patterns. Neonatal varicella, an early infection not associated with
birth defects, can occur via placental transmission in late pregnancy or via exposure to
maternal respiratory droplets shortly after birth.
H—Hepatitis: Both hepatitis B and C are concerns during pregnancy and can be transmitted
whether the child is born vaginally or via C-section. Hepatitis B is more likely to
be transmitted if the mother has an acute infection or a chronic infection and is
HBeAg1 (lacks antibodies to the e antigen). Infants born to mothers infected with
hepatitis B should receive hepatitis B immunoglobulin and the first dose of the
hepatitis B vaccine within hours of birth to decrease the likelihood of infection.
Those infants infected with hepatitis B during childbirth have a higher likelihood
(about 90%) of becoming chronically infected themselves. Women with chronic
hepatitis C have about a 4% chance of passing the infection on to their children.
E—Enterovirus: Non-polio enteroviruses are very common, specifically in the summer and fall.
Mothers infected shortly before delivery can potentially pass the infection on to the
infant. Infected infants will most likely have mild disease. According to the Centers
for Disease Control and Prevention (CDC), there is no clear evidence that infection
during pregnancy increases the risk of miscarriage, stillbirth, or congenital defects.
A—AIDS: HIV transmission can occur anytime during pregnancy, labor and delivery, or during
breastfeeding. Prior to the use of antiretroviral therapy (ART) in pregnancy, risk of
transmission to the infant was .90%. Risk of transmission is determined by several
factors, including the mother’s HIV viral load and use of or lack of antepartum or
intrapartum antiretroviral drugs. The CDC recommends that maternal ART should
be initiated as early in pregnancy as possible and continued by the infant for at least
4–6 weeks. Those infants born to HIV-positive mothers who did not receive
intrapartum ART should be initiated on ART prophylaxis within hours after birth.
With proper HIV treatment during pregnancy and after, risk of transmission can be
reduced to ,1%.
P—Parvovirus B-19: Parvovirus B-19 causes erythema infectiosum (slap face); fortunately, most women
are immune prior to pregnancy. Infection during pregnancy can cause a severe fetal
aplastic anemia and resultant complications (hydrops fetalis) leading to miscarriage.
64
CHAPTER 27 CONGENITAL AND PERINATAL INFECTIONS
O—Other: This is the catch-all for the mnemonic and includes: Group B Strep (GBS), Listeria,
Lyme, and Zika. Others may be added over time.
Group B Strep: GBS is a bacteria that can be passed to the infant during childbirth. Since 25% of
women carry GBS in their reproductive tract (are carriers/are colonized), the CDC
recommends routine screening of pregnant women for GBS between 35 and 37 weeks
of pregnancy. Those women who test positive or have an unknown GBS status are
treated with intravenous (IV) antibiotics during delivery to decrease the risk of
transmission to the infant. Infants that contract GBS during childbirth may become
ill and develop pneumonia, sepsis, and/or meningitis.
Listeria: Pregnant women are at a greater risk than the general population at contracting
an infection with Listeria monocytogenes, specifically during the third trimester.
Infection can manifest as flulike symptoms and can cause miscarriage or premature
delivery. About 20% of perinatal listeria infections will result in stillbirth or neonatal
death. Neonatal infections can cause sepsis, meningitis, and/or granulomatous
infantisepticemia. Foods to avoid during pregnancy include pate, young cheeses,
raw milk, and unwashed fruits and vegetables.
Lyme Disease: The CDC reports that untreated Lyme disease during pregnancy may potentially
cause brain, nerve, spinal cord, and cardiac defects. Avoidance of tick exposure during
pregnancy and early treatment of pregnant females is highly recommended. Since
doxycycline is contraindicated in pregnancy, treatment would consist of either
amoxicillin or cefuroxime in penicillin-allergic patients.
Zika: The CDC reports that Zika infection during pregnancy may cause congenital Zika
syndrome, a pattern of birth defects that includes microcephaly, decreased brain
development and mental retardation, ocular abnormalities, club foot, and/or
increased muscle tone at birth.
65
PART 3 CHILDHOOD ILLNESSES
C—Cytomegalovirus: Cytomegalovirus (CMV) can be passed to the fetus via the placenta if the mother has
an active infection. The CDC has recognized that most congenital CMV infections
are asymptomatic and/or never cause any long-term consequences. However, CMV
may cause spontaneous abortion or stillbirth. Signs of congenital CMV infection
include premature birth, low birth weight, microcephaly, seizures, mental retardation,
or hearing and/or vision loss. Hearing loss may be present at birth or may manifest
later in life.
E—Everything Sexually Another catch-all for the mnemonic. Both gonorrhea and chlamydia can be con-
Transmitted: tracted by the infant via vaginal delivery or in C-section if there has been premature
rupture of membranes. Both infections typically present as conjunctivitis (ophthalmia
neonatorum). A purulent conjunctival discharge 2–5 days after birth is classic for
gonorrhea, while a more watery (eventually progressing to purulent) discharge
occurring 5–14 days after birth is classic for chlamydia. Erythromycin ophthalmic
ointment can be used as prophylaxis in the infant against gonorrheal conjunctivitis,
but it has no effect on chlamydial conjunctivitis. Gonorrhea contracted at birth can
also cause infection in an infant’s pharynx, urethra, anus, and/or vagina, as well as
disseminated infections presenting as sepsis, meningitis, and/or arthritis. Chlamydial
infections contracted at birth can cause neonatal pneumonia.
S—Syphilis: Congenital syphilis occurs when the spirochete Treponema pallidum is passed to
the fetus via the placenta during pregnancy and may result in prematurity, LBW,
miscarriage, congenital infection, stillbirth, or neonatal death. The likelihood of the
mother passing the infection on to the fetus is highest in primary and secondary
syphilis and lowest in the tertiary stage. The CDC reports the risk of stillbirth or
neonatal death is near 40% for pregnant women with untreated syphilis. Of those
born with congenital infection, the disease is characterized as either early (diagnosed
before 2 years of age) or late (diagnosed after 2 years of age).
Early congenital syphilis presents with jaundice, hepatosplenomegaly,
lymphadenopathy, rhinitis (snuffles), a characteristic maculopapular rash, and
radiographic long bone abnormalities. Late congenital syphilis can present with
notched upper incisors (Hutchinson teeth), perioral fissures (rhagades), interstitial
keratitis, deafness, frontal bossing, saddle nose deformity, short maxilla and
protruding mandible, anterior bowing of the lower legs (saber shins), and arthritis
of the knees (Clutton joints). Hutchinson triad consists of deafness, Hutchinson
teeth, and interstitial keratitis. Children with congenital syphilis should be treated
with penicillin.
66
CHAPTER 27 CONGENITAL AND PERINATAL INFECTIONS
Chickenpox
Hepatitis
Enteroviruses
AIDS
pARvOVIRUS b-19
Toxoplasmosis
Other
(GBS, LIsteria, Lyme)
Rubella
CMV
Herpes Simplex
Everything
Sexually Trasmitted
syphillis
67
PART 3 CHILDHOOD ILLNESSES
Signs and Symptoms: Pertussis is divided into three stages. The Catarrhal Stage presents like most upper
respiratory infections with rhinorrhea, sneezing, low-grade temperature, and a
mild cough. These symptoms persist for about 7–10 days until the cough becomes
progressively worse. The Paroxysmal Stage is characterized by coughing spells or
paroxysms, the classic inspiratory whoop, and posttussive vomiting. Paroxysms
occur more frequently at night, increase in frequency for the first few weeks, remain
at a constant frequency for several weeks, and then gradually decrease in frequency.
Complications can include exhaustion, rib fractures, subconjunctival hemorrhages,
pneumonia, cyanosis, and apnea in children. The paroxysmal phase lasts 1–6 weeks,
but sometimes as long as 10. The Convalescent Stage is a gradual recovery associated
with less frequent and less persistent paroxysms. This stage lasts about 7–10 days
but can persist for as long as 21 days. Subsequent upper respiratory infections may
trigger paroxysmal coughing spells months after pertussis has resolved.
Diagnostic Testing: A nasopharyngeal swab should be used to obtain patient samples for both culture
and polymerase chain reaction (PCR) testing. Culture and PCR specimens can be
obtained immediately at the onset of cough and provide accurate results if obtained
in the first 2 weeks (culture) or 4 weeks (PCR) of symptoms. Serology can be
obtained between 2 to 8 weeks after cough onset and are of greater value later in
disease presentation.
68
CHAPTER 28 PERTUSSIS
Pertussis
tella pertu
(Whooping Cough) de
ss
Bo
is
(100-Day Cough)
am
Gr
c
bi
Co Aero
Incubation: 4–21 Days cco b a cill us
Average Incubation: 5–10 Days
Catarrhal Stage: 1–2 Weeks
Paroxysmal Cough Stage: 1–6 Weeks
Convalescence: Weeks to Months
Paroxysmal Stage
Coughing Spells/Paroxysms
Catarrhal Stage
Runny Nose
Sneezing Inspiratory Whoop
Low-grade Temperature Posttussive Vomiting
Mild Cough Cyanosis
Apnea in Infants
Subconjunctival Hemorrhage
Cough Becomes Worse
Rib Fractures/PTX
Cough, cough Pneumonia
WHOOP!
Paroxysms are
worse at night!
69
PART 3 CHILDHOOD ILLNESSES
Peak Incidence: Spring–Fall, Occasional outbreaks in day care centers and elementary schools
Brief Description: Hand, foot, and mouth disease (HFMD) is a self-limiting febrile viral enanthem of the
mouth with associated papular, maculopapular, or vesicular rash of the hands and
feet. The disease is most common in children under the age of 10, with most cases
occurring in children younger than 5 years of age.
Signs and Symptoms: HFMD classically presents as a low-grade fever, headache, and malaise for 1–3 days,
followed by an oral enanthem with a papular, maculopapular, or vesicular rash of
the hands and feet. The rash may occasionally involve the legs and buttocks. The
sores in the mouth may cause poor feeding and irritability. The disease is self-limiting
and tends to resolve after 7–10 days. Fingernail and toenail loss can occur in some
children 4–8 weeks after infection with HFMD.
Diagnostic Testing: HFMD tends to be a clinical diagnosis based on history, symptoms, and characteristic
exam findings.
Prevention: Handwashing. Enteroviruses tend to be transmitted via the fecal-oral route. HFMD
can be transmitted via oral and nasal secretions, as well as via the fecal-oral route.
70
CHAPTER 29 HAND, FOOT, AND MOUTH DISEASE
En o
16 1
C
7
Incubation: 3–6 Days
Fever 1–3 Days Rash
ssRNA
Common: <5 Years Old
Self-Limiting: 7–10 Days
Peak: Spring–Fall
Fever
Headache
Sore Throat Malaise
Poor Feeding
Rash Occasionally
on Legs/Buttocks
71
PART 3 CHILDHOOD ILLNESSES
Description: Bronchiolitis is an acute viral lower respiratory tract infection most commonly caused
by RSV in children less than 2 years old. Bronchiolitis peaks in infants 3–6 months old
and is the most common cause for hospitalization in children younger than 1 year old.
Infants with higher risk for severe disease include preemies, low–birth weight infants,
and those born with congenital heart defects.
Signs and Symptoms: RSV affects both children and adults, often presenting as a typical viral upper
respiratory infection with possible wheezing in the latter. In young children,
bronchiolitis initially presents with rhinorrhea and then progresses to the lower
respiratory tract after a few days. Inflammation of the smaller airways (bronchioles)
causes cough, wheezing, and rhonchi. Severe disease is characterized by lethargy,
poor feeding, tachypnea, nasal flaring, retractions, hypoxia, cyanosis, apnea, and
respiratory failure. Infants younger than 4 weeks of age and smaller, low birth–weight,
premature infants (preemies) are at higher risk of central apnea. Symptoms tend to
resolve after 7–10 days.
Diagnostic Testing: Diagnosis is often based on history and clinical presentation. Chest x-ray may show
hyperinflation and peribronchial cuffing. Nasopharyngeal swabs can be used to
obtain samples for polymerase chain reaction (PCR) testing in the acute setting.
IgM/IgG serology exists but is of limited value in the acutely ill patient.
Treatment: Treatment is mostly supportive. Management and disposition is based on patient age,
past medical history, risk factors for apnea, and severity of illness. Nasal suctioning
helps clear secretions. Supplemental oxygen and a trial of bronchodilators are
beneficial. Steroids, antibiotics, and/or ribavirin have no proven benefits. Intravenous
fluids may be necessary given insensible losses and decreased oral intake.
72
CHAPTER 30 BRONCHIOLITIS
Bronchiolitis
RSV #1
Metapneumovirus
Incubation: 3–5 Days Influenza/Parainfluenza
Children <2 Years Old Adeno/Corona/Rhino
Most 3–6 Months Old
Viruses
Risk: Preemies/LBW
Congenital Heart Disease
Winter Peak
#1 Cause of Hospitalization
<1 Years Old
Cough
Wheezing Lethargy
Poor Nasal
Feeding Flaring
Tachypnea
Apnea
Retractions
Cyanosis
73
PART 3 CHILDHOOD ILLNESSES
Incubation: Unknown
Geographic Regions Affected: Worldwide, with greatest incidence in Japan and East Asian countries. Children of
East Asian and Pacific Island descent living worldwide are affected to a greater
degree than Caucasians.
Signs and Symptoms: The disease begins with irritability and a high fever that tends to be unresponsive to
traditional antipyretics. Children will likely next develop bilateral conjunctivitis and
inflammation of the oral mucosa, including cracked red lips, inflamed “strawberry
tongue,” and/or oropharyngeal erythema. Rash, typically occurring 1–2 days after
fever onset, is polymorphic and can be erythematous, macular, maculopapular,
desquamating, or target-like and involves the trunk and extremities. Hand and foot
erythema and edema are the last symptoms to appear. Periungal desquamation can
occur in the convalescent phase of the disease. Lymphadenopathy, when it occurs, is
limited to the anterior cervical chain. Without treatment, the disease resolves within
10–12 days. Coronary artery aneurysms can develop in untreated patients as the
disease resolves, thus early diagnosis and treatment with intravenous immunoglobulin
(IVIG) is paramount.
Diagnostic Testing: Labs will reveal elevated CRP and SED rates, leukocytosis with a left shift (increased
neutrophils), increased platelets, and normocytic anemia.
Diagnostic criteria established by Tomisaku Kawasaki require the presence of a
fever .5 days’ duration and four of the five following criteria: (1) bilateral conjunctival
injection, (2) polymorphous rash, (3) cervical lymphadenopathy with one node at
least .15 mm, (4) strawberry tongue, cracked lips, or injected pharynx, (5) hand or
foot erythema, edema, or periungal desquamation.
Treatments: IVIG is the standard treatment and is ideally initiated within 7–10 days to decrease
the likelihood of coronary artery aneurysms. High-dose aspirin tapered down over
time is still a part of some treatment protocols.
Pearls: Diagnostic criteria for KD can be remembered by the mnemonic: Fever .5 Days
and CRASH: Conjunctivitis, Rash, Adenopathy, Strawberry tongue, Hands and Feet.
74
CHAPTER 31 KAWASAKI DISEASE
Kawasaki Disease
Fever >5 Days
C Conjunctivitis
(Bilateral)
I nfe
e
un
tio
us/Autoi mm
R
c
Rash
(Trunk/Polymorphic)
A Adenopathy
(>15 mm cervical)
S Strawberry Tongue
(Red throat) Conjunctivitis
High Fever
>5 Days
Polymorphous
Periungual Rash
Desquamation
(Convalescent)
Hand/Foot
Edema &
Erythema
75
PART 3 CHILDHOOD ILLNESSES
Causative Agents: ssRNA Parainfluenza virus is the most common cause. Other viral causes can include
influenza virus, respiratory syncytial virus, human metapneumovirus, adenovirus,
and rhinovirus.
Peak Incidence: Fall–Winter. Most common in children 6 months to 3 years old, with a peak
incidence at age 2.
Description: Croup is a viral infection of the upper airway that causes stridor, hoarseness, and a
characteristic bark-like cough, often worse at night.
Signs and Symptoms: Croup is often preceded by a prodrome of several days of malaise, rhinorrhea, and
a low-grade fever before the onset of hoarseness, stridor, and the characteristic
seal-like barking cough. The Westley Croup Score categorizes the severity of
illness on the basis of five criteria: chest wall retractions, stridor, cyanosis, level of
consciousness, and air entry. Fortunately, most cases are mild and can be managed
as an outpatient or with overnight observation. Symptoms often resolve in most
patients within 3–7 days.
Diagnostic Testing: Croup tends to be a clinical diagnosis based on history, symptoms, and characteristic
exam findings. An anterior-posterior (AP) soft tissue neck x-ray will likely reveal
the “steeple sign,” a tapering of the upper trachea resembling a church steeple.
Astute clinicians need to consider epiglottitis (drooling and high fever) and bacterial
tracheitis (toxic appearance and high fever) in their differential.
Treatments: Supportive. Steam or humidified mist may be of some benefit in providing calm for
both the infant and family. Nebulized epinephrine can be given every 20 minutes
and decrease upper airway edema and stridor. Oral corticosteroids (dexamethasone)
take effect within 6 hours of administration, decrease the frequency of nebulized
epinephrine treatments, and shorten the emergency department/hospital lengths
of stay.
76
CHAPTER 32 CROUP
Croup fluenza V
ain i
(Laryngotracheobronchitis)
ru
Pa
s
ssRNA
Bark!
Bark!
Bark!
Bark!
Bark!
Bark!
Steeple Sign
77
PART 4
TICK-BORNE
ILLNESSES
PART 4 TICK-BORNE ILLNESSES
Relapsing Fever: • Causative Agent: Borrelia hermsii, Borrelia parkeri, Borrelia duttoni, Borrelia
miyamotoi
• Vector: Ornithodoros species (soft body ticks)
• Region: Africa, Spain, Middle East, Western United States, and Canada
• Symptoms: relapsing fevers, headaches, myalgia, cough, rash
• Treatment: doxycycline, tetracycline, erythromycin
80
CHAPTER 33 TICK-BORNE ILLNESS AND TICKS AS VECTORS
Colorado Tick Fever: • Causative Agent: Colorado tick fever virus (CTFV)
• Vector: Dermacentor andersoni (Rocky Mountain wood tick)
• Region: Western U.S.
• Symptoms: Two phases of disease. Initially fever, chills, headache, malaise, myalgia,
nausea, vomiting, splenomegaly, rash. In the second phase, symptoms intensify.
• Treatment: supportive
81
PART 4 TICK-BORNE ILLNESSES
Tick-Borne Illnesses
Tick-Borne
Meningoencephalitis
Relapsing Fever
Rocky Mountain
Spotted Fever
e on
It’s m nee
k
the
Lyme
Disease
Tularemia
Tick Paralysis
82
CHAPTER 33 TICK-BORNE ILLNESS AND TICKS AS VECTORS
Ticks as Vectors
Ixodes Scapularis
• Lyme Ixodes Pacificus
• Tick-Borne Meningoencephalitis • Lyme
• Babesiosis • Babesiosis
• Anaplasmosis • Anaplasmosis
Ornithodoros
American • Relapsing Fever Ixodes Ricinus
Dog/Wood • Lyme
(D. variabilis) Lone Star • Tick-Borne Meningoencephalitis
• Tularemia • Ehrlichiosis • Helvetica Spotted Fever
R.M. Wood • Ehrlichiosis • Tularemia • Babesiosis
(D. andersoni) • Tick Paralysis • Anaplasmosis
• RMSF • RMSF
• Tularemia
• Tick Paralysis
• Colorado Tick Fever
83
PART 4 TICK-BORNE ILLNESSES
Vector: United States: American dog tick (Dermacentor variabilis), Rocky Mountain wood
tick (D. andersoni), brown dog tick (Rhipicephalus sanguineus). Central and South
America: Cayenne tick (Amblyomma cajennense). Female ticks pass the infection to
their eggs in a process called transovarial transmission.
Geographic Regions Affected: North Atlantic and South Central regions of the United States, North America, Central
America, and South America.
Signs and Symptoms: Patients with mild disease have fever, malaise, myalgia, nausea, vomiting, headache,
arthralgia, and rash. The characteristic rash of RMSF is a centripetal “inward”
spreading macular rash, beginning on the wrist, forearm, and ankles and spreading
inward toward the trunk. The palms and soles are involved in up to 80% of patients.
Patients with severe disease may have skin necrosis, digit gangrene, acute respiratory
distress syndrome, pulmonary edema, nausea, vomiting, abdominal pain, diarrhea,
confusion, acute renal failure, meningoencephalitis, ataxia, blindness, retinal
hemorrhages, papilledema, disseminated intravascular coagulation, jaundice,
rhabdomyolysis, hepatomegaly, stupor, circulatory shock, and death.
Diagnostic Testing: The disease should be considered in patients presenting with fever, rash, and history of tick
exposure/bite. Labs will reveal hyponatremia, thrombocytopenia, elevated liver enzymes,
increased bilirubin, and increased BUN. Serologic detection of a fourfold rise in IgG
antibodies against R. rickettsii by indirect immunofluorescence assay; Western blot with
cross-absorption; detection of rickettsial nucleic acids by PCR in blood, skin biopsy, and
eschar biopsy or swab; immunohistochemical detection of R. rickettsia in skin biopsy.
Treatments: Doxycycline 100 mg twice a day for 7–10 days. Chloramphenicol can be used as an
alternative in pregnancy, but has a wide range of side effects and requires blood
monitoring.
Pearls: Prevention by avoidance of tick exposures and early removal of attached ticks.
Early therapy improves outcomes and prevents severe complications or sequelae.
More-severe infections are seen in males, alcoholics, the elderly, African Americans,
the immunocompromised, and patients with G6PD deficiency. Fever without rash can
occur in the elderly and African Americans.
84
CHAPTER 34 ROCKY MOUNTAIN SPOTTED FEVER
R ic
tsi
i
Incubation:
2–14 Days Gram Obligate
Intracellular
Bacteria
Transmission in
American
6–10 Hours of Bite Dog/Wood Tick
Headache
Rocky Mountain
Wood Tick
Centripetal
Rash Nausea
Vomiting Brown
Dog Tick
Myalgia
Fever
Malaise
Myalgia
Nausea
Headache
Arthralgia
RASH
in 3–5 Days
of Fever
85
PART 4 TICK-BORNE ILLNESSES
Causative Agents: Borrelia burgdorferi in North America; B. afzelii and B. garinii in Europe
Vector: Deer tick (Ixodes scapularis) in Eastern U.S., black-legged tick (Ixodes pacificus) in Western
U.S., sheep tick (Ixodes ricinus) in Europe, taiga tick (Ixodes persulcatus) in parts of Asia
Geographic Regions Affected: Northern latitudes of North America, Europe, and Asia
Peak Incidence: Spring through fall, with peaks in summer months, in accordance with the activity of
nymph stage of Ixodes spp. ticks. Nymphs are more likely than adult ticks to transmit
Lyme disease.
Description: Lyme disease is a tick-borne spirochetal zoonosis that may affect the skin, joints,
nervous system, and heart. The disease is broken down into three stages of infection:
early localized, early disseminated, and late disseminated.
Signs and Symptoms: Early localized infection is characterized by a circular, outwardly-expanding bull’s-eye
rash known as erythema migrans (EM), occurring in 70%–80% of patients. Flulike
symptoms, including fatigue, malaise, headache, myalgia, and fever, may be present
or delayed. Early disseminated infection occurs within several days to weeks of
the initial EM lesion and can present as multiple areas of EM. Within months,
patients may develop neurologic symptoms, including facial palsy (can be bilateral),
photosensitivity, polyneuropathy, vertigo, ataxia, insomnia, memory loss, psychosis,
meningitis, and encephalitis. Cardiac symptoms can also present that include
myopericarditis and heart block. Late disseminated infection is characterized by
chronic arthritis and joint effusions, usually involving the knee.
Treatments: For early infection: doxycycline 100 mg orally twice a day, amoxicillin 500 mg orally
three times a day, or cefuroxime 500 mg orally twice a day for 14–21 days. Treatment for
cardiac, nervous system, or joint involvement: ceftriaxone 2 g intravenously once a day
for 28 days can be used. Treatment regiments may vary based on severity of disease.
Pearls: Prevention by avoidance of tick exposure and early removal of attached tick.
Transmission rarely occurs unless the tick has been attached for .24 to 36 hours.
Early therapy improves outcomes and prevents severe complications or sequelae.
When an engorged nymph is found attached, a single dose of 200 mg of oral
doxycycline given within 72 hours of the tick bite can prevent Lyme disease.
Multiple EM indicates spirochetemia and not multiple tick bites. Coinfection with
Babesia microti can occur. Lyme disease is the most common vector-borne infection
in the United States and is very common in the Northeast and upper Midwest U.S.
86
CHAPTER 35 LYME DISEASE
Lyme Disease
Spring–Fall
Incubation:
3–30 Days
Peak: Summer
Headache
Conjunctivitis
Transmission
in 24–36 Hr
of Bite
Facial Droop
Multiple EM =
Spirochetemia
Cardiomyopathy
AV Block
Joint
Effusion
Ixodes
scapularis
87
PART 4 TICK-BORNE ILLNESSES
Vector: Lone star tick (Amblyomma americanum), dog tick/wood tick (Dermacentor variabilis)
Signs and Symptoms: Many cases are thought to be asymptomatic. In mild disease, fever, chills, headache,
malaise, myalgia, nausea, vomiting, diarrhea, conjunctivitis, and rash can occur.
Unlike HGA, rash occurs in about 30% of adults and up to 60% of children
with HME. In severe disease, septic shock-like syndrome, respiratory distress,
meningoencephalitis, renal failure, and death can occur. Severe disease is more
common in immunosuppressed, HIV-positive, elderly, or asplenic patients.
Diagnostic Testing: Labs will reveal leukopenia, thrombocytopenia, anemia, elevated liver enzymes,
increased LDH. Serologic detection of a fourfold rise in antibodies against Ehrlichia
chaffeensis by immunofluorescence assay; detection of bacterial DNA in blood or
cerebrospinal fluid by PCR; and peripheral blood smear examination for morulae in
monocytes.
Pearls: Prevention by avoidance of tick exposure and early removal of attached ticks.
Diagnosis is often based on history and clinical suspicion. Consider the diagnosis
in patients presenting with fever, leukocytosis, thrombocytopenia, abnormal liver
enzymes, elevated LDH, and a history of tick bite. Early therapy improves outcomes
and prevents severe complications or sequelae. Treatment response is expected
within 48 hours and failure to respond within 3 days suggests infection with a
different agent. Doxycycline is indicated for use in children of any age, according
to the CDC and American Academy of Pediatrics. There can be coinfection with
Rickettsia rickettsii.
88
CHAPTER 36 EHRLICHIOSIS
Ehrlichiosis - HME
A n a p l a s ma
is I nt ra c
a te e
ph u la r
O bl n
e
chaffe
ago
ig
ll
Spring & Summer
c y to p h i
cytes
ch ia
o
Leuk
li
lu
hr
m
E
Incubation:
7–14 Days
Headache
Fever
DX: Fever (Common)
+
Tick Bite Myalgia
+
WBC/ Plt
ALT/AST/ALP
LDH
Rash
HME = Uncommon
HGA = Rare
Arthralgia
Vector: Deer tick (Ixodes scapularis) in Eastern United States; black-legged tick (Ixodes
pacificus) in Western United States; sheep tick (Ixodes ricinus) in Europe; taiga tick
(Ixodes persulcatus) in parts of Asia; cattle tick (Haemaphysalis longicornis) in China
Geographic Regions Affected: Northern latitudes of North America, Europe, and Asia
Signs and Symptoms: Many cases are thought to be asymptomatic. When symptomatic, about two thirds of
patients develop fever, chills, malaise, headache, nausea, vomiting, diarrhea, cough,
arthralgia, stiff neck, and myalgia. Rash is a rare finding in HGA. One third of patients
can have severe disease with respiratory insufficiency, septic shock-like illness,
rhabdomyolysis, renal failure, meningoencephalitis, hemorrhage, and opportunistic
viral and fungal infections that can lead to death. Severe disease is more common in
immunosuppressed, HIV, elderly, or asplenic patients.
Diagnostic Testing: Labs will reveal leukopenia, thrombocytopenia, anemia, elevated liver enzymes,
and elevated LDH. Peripheral blood smear examination for morulae in circulating
neutrophils; detection of bacterial DNA in blood by PCR; serologic detection of a
fourfold rise in IgG antibodies against Anaplasm phagocytophilum.
Treatments: Doxycycline 100 mg twice a day for 10 days; rifampin has been successfully used in
children and during pregnancy.
Pearls: Prevention by avoidance of tick exposure and early removal of attached ticks.
Diagnosis is often based on history and clinical suspicion. Consider the diagnosis
in patients presenting with fever, leukocytosis, thrombocytopenia, abnormal liver
enzymes, elevated LDH, and a history of tick bite. Early therapy improves outcomes
and prevents severe complications or sequelae. There can be coinfection with
Borrelia burgdorferi or Babesia microti.
90
CHAPTER 37 ANAPLASMOSIS
Anaplasmosis - HGA
A n a p l a s ma
is I nt ra c
a te e
ph u la r
O bl n
e
chaffe
ago
ig
ll
Spring & Summer
c y to p h i
cytes
ch ia
o
Leuk
li
lu
hr
m
E
Incubation:
7–14 Days
Headache
Fever
DX: Fever (Common)
+
Tick Bite Myalgia
+
WBC/ Plt
ALT/AST/ALP
LDH
Rash
HME = Uncommon
HGA = Rare
Arthralgia
Vector: Deer tick (Ixodes scapularis); black-legged tick (Ixodes pacificus), sheep tick (Ixodes
ricinus) in Europe
Geographic Regions Affected: Northeastern United States and Upper Midwest (Babesia microti), Pacific Northwest
(Babesia duncani), and parts of Europe (Babesia divergens)
Peak Incidence: May through September. The initial infection occurs in late spring to early summer,
in accordance with the activity of nymph stage of Ixodes spp. ticks. Since there is a
1- to 6-week incubation period, 50% of the cases are seen in July and 25% in August.
Adult ticks may cause infection in late summer or early fall.
Description: Babesiosis is a tick-borne protozoan zoonosis that causes the lysis of host erythrocytes.
The disease can range from mild to severe and has symptoms resembling malaria.
Signs and Symptoms: Mild Disease: weakness, fatigue, malaise, fever, chills, night sweats, headache, myalgia,
anorexia, cough, arthralgia, nausea, vomiting, diarrhea, neck stiffness, and hemolytic
anemia. Severe Disease: ARDS, CHF, DIC, liver failure, splenic infarct and rupture,
and kidney injury. Coma and death can ensue.
Diagnostic Testing: Labs will reveal hemolytic anemia, elevated liver enzymes, increased bilirubin,
thrombocytopenia, and leukopenia. Giemsa-stained peripheral blood smear
examination for ring trophozoites or Maltese cross-shaped tetrads of merozoites in
erythrocytes; detection of parasitic 18S rRNA gene by PCR serologic detection of
IgM and IgG antibodies.
Pearls: Prevention by avoidance of tick exposures and early removal of attached ticks. Early
therapy improves outcomes and prevents severe complications or sequelae. There
can be coinfection with Borrelia burgdorferi or Anaplasm phagocytophilum. It can be
transmitted by blood transfusion and via the placenta. Immunosuppressed, asplenic,
and patients older than 50 years of age are at increased risk for severe disease. While
B. divergens, B. odocoilei, B. venatori, and B. bigemina are more commonly associated
with various animals, human infection can occur but is rare.
92
CHAPTER 38 BABESIOSIS
ot
Ba
May–September
i
Pr
otozo
a
Ba
be
ni
s i a d u n ca
Incubation:
1–6 Weeks
Night
Sweats
Fever ARDS
Chills
CHF
DIC
Liver
Failure
Malaise
Weakness AKI
Splenic
Maltese Cross Infarct
Babesia
Thin Smear
Wright’s or Giemsa Stain
93
PART 4 TICK-BORNE ILLNESSES
Vector: American dog/wood tick (Dermacentor variabilis), Rocky Mountain wood tick
(Dermacentor andersoni), lone star tick (Amblyomma americanum), and deer flies
(Chrysops callidus). Mosquitoes in Europe.
Reservoir: Lagomorphs: rabbits, hares, and pikas; aquatic rodents: beavers and muskrats
Peak Incidence: April through October, with a peak in June and July due to ticks
Description: Tularemia is a gram-negative zoonotic bacterial disease associated with rabbits that
presents as one of six clinical variants. It is transmitted by tick or deerfly bites or
from contact with infected host animals.
Signs and Symptoms: Ulceroglandular: Painful skin ulcer at the site of insect bite or animal exposure
with associated regional tender lymphadenopathy. The lymph nodes may become
suppurative.
Glandular: Regional lymphadenopathy without evidence or recall of skin ulceration.
Oropharyngeal: Fever and sore throat predominate, with cervical, preparotid,
and retropharyngeal lymphadenopathy. Nausea, vomiting, and diarrhea can occur.
The source of infection is associated with the ingestion of contaminated water or
undercooked contaminated animal meat.
Pneumonic: Fever, dyspnea, and pneumonia predominate and are caused by the
direct inhalation of aerosolized bacteria or from hematogenous spread.
Oculoglandular: Often unilateral and caused by conjunctival exposure to the bacteria.
Presenting symptoms include conjunctivitis and preauricular lymphadenopathy.
Typhoidal: Febrile illness without lymphadenopathy. Symptoms can include fever,
chills, malaise, anorexia, headache, myalgia, nausea, vomiting, diarrhea, and
abdominal pain. Illness can progress to cause meningoencephalitis, hepatosplenomegaly,
cholangitis, hepatitis, liver abscess, necrotic bowel, shock, kidney failure, rhabdomyolysis,
pneumonia, and death.
Diagnostic Testing: Specimens from swabs or scraping of skin lesions, lymph node aspirates or
biopsies, pharyngeal washings, sputum, or gastric aspirates can be used for culture,
immunostaining, and PCR. Acute and convalescent serologic titers can be followed.
Treatments: Mild disease can be treated with oral doxycycline 100 mg or ciprofloxacin 500 mg
twice a day for 14 days. Moderate to severe disease requires streptomycin or
gentamicin, with the addition of doxycycline or chloramphenicol when meningitis
is present.
94
CHAPTER 39 TULAREMIA
ns
Fra
is
t
ill r
m ra c e ll ul c
In
us
Incubation: 1–14 Days American
Gra
a
Average 3–5 Days Dog Tick co cco ba
Typhoidal
+ Febrile Illness
- Lymphadenopathy
Oculoglandular
Oropharyngeal
Ulceroglandular
Glandular
Fever/Chills
Pneumonic
Oropharyngeal:
Hunters
Pharyngitis with Cervical
Trappers Lymphadenopathy
or
Butchers GI Symptoms
Farmers
95
PART 4 TICK-BORNE ILLNESSES
Reservoir: Many wild and domestic animals including cattle, goats, sheep, hares, and ostriches.
Incubation Period: Tick bite: 1–3 days; exposure to infected blood: 5–6 days
Geographic Regions Affected: Africa, the Balkans, Eastern Europe, Middle East, and Asia
Peak Incidence: Between March and May and a second peak between August and October.
Description: CCHF is a tick-borne zoonotic viral hemorrhagic fever spread via the Hyalomma
spp. ticks and/or exposure to infected blood via the slaughter and butchering of
domestic livestock. Human-to-human transmission is possible via contact with
infected blood or surgical instruments.
Signs and Symptoms: After the incubation period, there is a 3-day–long prehemorrhagic phase characterized
by the sudden onset of facial flushing, malaise, myalgia, dizziness, diarrhea, nausea,
vomiting, headache, high fever, back pain, arthralgia, stomach pain, conjunctivitis,
pharyngitis, and petechiae on the palate. The hemorrhagic phase occurs next, between
days 3 and 5 and lasts for up to 2 weeks. The hemorrhagic phase is characterized by
gingival bleeding, ecchymosis, epistaxis, mucosal bleeding, hematemesis, melena,
hematuria, hemoptysis, and abdominal muscle hematomas. Females can have vaginal
and uterine bleeding. There may be hepatosplenomegaly, massive liver necrosis,
hemorrhagic pneumonia, cardiovascular disturbances, changes in mood and sensory
perception, multisystem organ failure, cerebral hemorrhage, shock, and death between
the days 5 and 14 of illness. Fatality rate averages 30% and ranges between 5% and 80%.
Diagnostic Testing: Polymerase chain reaction (PCR), serology for IgM and IgG antibodies, and viral
recovery in cell cultures.
Treatments: Supportive care. Ribavirin and platelet transfusion may be useful. Recovery is slow.
Pearls: Ticks can serve as both vectors and reservoirs. Livestock serve as amplifying hosts of
the disease and, if infected, put herders and butchers at risk of infection, specifically
through exposure to infected animal blood.
96
CHAPTER 40 CRIMEAN-CONGO HEMORRHAGIC FEVER
Incubation: ssRNA
Incubation
Prehemorrhagic
Days 1–3
RIP
Hemorrhagic
Days 3–5 30%
Recovery Death Hyalomma
97
PART 4 TICK-BORNE ILLNESSES
Causative Agents: Colorado tick fever virus, Coltivirus (Colorado tick virus)
Geographic Regions Affected: Rocky Mountain region of the United States at altitudes from 4000 to 10,000 feet
with rocky outcroppings. Also found in Europe and China.
Description: Colorado tick fever is a tick-borne viral zoonosis that infects erythrocytes and is
characterized by flu-like symptoms and a saddleback fever pattern.
Signs and Symptoms: Saddleback (biphasic) fever pattern with an initial 3-day phase with abrupt onset of
fever, chills, headaches, pharyngitis, retro-orbital pain, photophobia, conjunctivitis,
myalgia, generalized malaise, abdominal pain, splenomegaly, nausea, vomiting,
diarrhea, and rash; remittance of symptoms for 1–3 days followed by a second 2-day
phase with high fever, worsening of symptoms, generalized weakness, lethargy,
aseptic meningitis, encephalitis, and hemorrhagic fever. It may rarely cause
myocarditis, pericarditis, pneumonitis, and hepatitis. Children are at risk of death
from hemorrhagic shock, meningoencephalitis, or disseminated intravascular
coagulation. Full resolution of symptoms typically occurs within 1 week.
Diagnostic Testing: Labs will reveal leukopenia, thrombocytopenia, and elevated liver enzymes. PCR
testing of blood or CSF is diagnostic in the first few days of infection, while serology
is often negative in the first 2 weeks after symptom onset.
Treatments: Supportive. Avoid aspirin in children due to increased risk of Reye syndrome, and
avoid nonsteroidal antiinflammatory drugs due to risk of bleeding secondary to
thrombocytopenia.
Pearls: Prevention by avoidance of tick exposures and early removal of attached ticks. Must
use gloves and tweezers close to the head of the tick for removal and wash the wound
with soap and water. Infection can occur even with brief tick attachment. It can be
transmitted by blood transfusion. Intrauterine transmission can lead to miscarriage
and congenital anomalies. Viremia may persist for up to 4 months.
98
CHAPTER 41 COLORADO TICK FEVER
s
sR
Incubation: 1–14 Days iru
s
d
NA
R eo -V
Average: 3–5 Days
Peak: June
Fever/Chills
Headache
Myalgia
Malaise “Biphasic”/”Saddleback”
Fever
99
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PART 5
WORMS
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1
PART 5
Section
ROUNDWORMS
PART 5 WORMS
Lifecycle: Immature eggs are passed in the feces to soil where they embryonate for 2–4 weeks
before becoming infectious. Infectious eggs can be consumed through poor
handwashing and sanitation or through ingestion of unwashed vegetables, particularly
where human waste is used as fertilizer. Once ingested, eggs hatch in the small
intestine, they invade intestinal mucosa, and are carried through the portal and
systemic circulatory systems to the lungs. Once in the lungs, the larvae mature over
2 weeks and penetrate the alveolar walls. Mature larvae are coughed up the bronchial
tree and are swallowed. Once swallowed, they migrate to the small intestine where
they mature into adult worms. The entire cycle takes 2–3 months and once mature,
worms live 1–2 years. Adult females produce about 200,000 eggs per day.
Geographic Regions Affected: Worldwide. There is a higher prevalence in underdeveloped, tropical nations with
poor sanitation, including parts of Asia, the Western Pacific, South America, and
Africa.
Signs and Symptoms: Most infections are asymptomatic unless there is significant worm burden. Shortness
of breath, cough, and fever may be present in the early phase of the disease followed
by abdominal pain, nausea, and diarrhea. Loffler syndrome can occur in early infections
with significant worm burden. Children with chronic infection can have malabsorption
of protein, fats, vitamin A, and iodine leading to malnutrition, and growth and
developmental delays. Individual worms may migrate to and potentially obstruct the
common bile duct, gallbladder, pancreatic duct, and appendix, causing organ-specific
symptoms. Significant worm burden may cause small bowel obstruction requiring
surgical removal.
Diagnostic Testing: Eosinophilia may be present on labs. Stool samples 33 to identify eggs.
Pearls: Ascariasis eggs are quite hardy and can survive up to 5–6 years, specifically in moist,
warm, shady soil. The hardiness of the eggs and large numbers released daily by
females leads to a high prevalence of the disease.
104
CHAPTER 42 ASCARIASIS
Ascariasis is
lumbric
ROUNDWORMS
oi
r
Asca
des
Ectopic Ascariasis
Ne
matode
Pancreas
GB
Appendix
Nasal Oropharyngeal
MOIST
SOIL WARM Fertilized Eggs
Unfertilized
Egg Dies
SHADE Develop in Soil
105
PART 5 WORMS
Subcutaneous Filariasis: Loiasis is caused by Loa loa (the eye worm) and is transmitted by female day-feeding
horse or deer flies of the genus Chrysops. The disease is common in West Africa and
is often asymptomatic unless there is a large worm burden. Calabar swellings are
localized patches of pruritic angioedema that correlate to worm migration. The Loa
loa worm can migrate to the conjunctiva of the eye and be visualized, giving rise to
its name. Treatment: DEC, which can also be given weekly as chemoprophylaxis to
travelers to endemic areas. Albendazole can also be used. The Loa loa worm is unique
among filarial worms as it does not harbor the Wolbachia symbiotic bacteria.
Onchocerciasis or River Blindness is caused by Onchocerca volvulus and is transmitted
by the female day-feeding black fly. The disease is common in West Africa, East
Africa, Arabian Peninsula, and South America. It is characterized by specific acute
and chronic cutaneous manifestations and is the second most common cause of
infectious blindness. Treatment: Ivermectin and doxycycline.
Streptocerciasis is caused by Mansonella streptocerca and is transmitted by the
midge. It is common in Central African rain forests and is often asymptomatic.
Pruritus and dermatitis are the predominant symptoms, and a cultured skin biopsy
will reveal microfilaria. Treatment: DEC or ivermectin.
Serous Cavity Filariasis: Two members of the Mansonella species are considered to reside within deeper
tissues, including the pleural and peritoneal cavities of humans. Most infections are
asymptomatic. Mansonella ozzardi can be found in northern parts of South America
and Central America. Symptoms can include pruritus, headache, malaise, fever,
arthralgia, and pulmonary manifestations. Treatment: Ivermectin. Mansonella
perstans can be found in sub-Saharan Africa and parts of Central and South America.
Symptoms can include pruritus, headache, malaise, fever, and arthralgia. Treatment
can be challenging, given resistance, and includes doxycycline and albendazole.
106
CHAPTER 43 FILARIASIS
Lymphatic Filariasis
ROUNDWORMS
(Elephantiasis)
e reria banc
ch
ro
Wu
Brugia malayi
ft
i
Brugia timori
Nematode
Lymphatic Wolbachia
Filaria Bacteria
107
PART 5 WORMS
Subcutaneous Filariasis
ROUNDWORMS
Mansonella streptocerca
Midge
Onchocerca
volvulus
108
CHAPTER 43 FILARIASIS
ROUNDWORMS
109
PART 5 WORMS
Lifecycle: The disease is spread from infected humans to other humans via the bite of the female
black fly. Black flies feed during daytime hours, when microfilaria migrate to the skin.
During a blood meal, infectious microfilaria are ingested and migrate to the gut and
thoracic muscles of the black fly. The larvae mature over the next week and migrate to
the proboscis of the fly. During the next feeding, larvae are passed on to the next host
where they migrate to the subcutaneous tissue and mature over the next 6–12 months.
Once mature, male and female worms mate and produce approximately 1000 microfilaria
per day. These microfilaria then migrate to the skin during the day, awaiting the bite
of the black fly to continue their lifecycle.
Geographic Regions Affected: West Africa, East Africa, Arabian Peninsula, South America
Signs and Symptoms: Skin changes of varying degrees are common. Acute and chronic papular dermatitis
(onchodermatitis), skin atrophy (lizard skin), depigmentation (leopard skin), and
lichenification (elephant skin) are characteristic. Pruritus is common. Corneal (eye)
involvement includes punctate keratitis that leads to scarring and blindness.
Diagnostic Testing: Clinical signs and symptoms in individuals from endemic areas lead one to suspect
the diagnosis. Slit lamp examination reveals microfilaria in the eye. Skin biopsies
plated in saline solution will cause microfilaria to emerge, confirming the diagnosis.
Prevention: Mass treatments with ivermectin and insect control programs have been used with
good success in some areas.
Pearls: Second most common cause of blindness due to infection. Ivermectin is effective at
killing the worms within the host, while doxycycline kills off a symbiotic bacteria
(Wolbachia) within the worms themselves.
110
CHAPTER 44 ONCHOCERCIASIS
Onchocerciasis c e r c a vo l v
ROUNDWORMS
ho
ul
c
(River Blindness)
On
us
Ne
matode
Microfilaria migrate to
the skin during the day.
I only feed
during the day! Infectious
Blindness
Chronic Papular
Onchodermatitis Acute Papular
Onchodermatitis
Skin Atrophy
Lichenified (Lizard Skin)
Onchodermatitis
(Elephant Skin)
Depigmentation
(Leopard Skin)
111
PART 5 WORMS
Synonym: Enterobiasis
Lifecycle: Eggs are deposited in the perianal area by female worms, mostly at night. Perianal
itching can cause autoinfection and/or eggs can be passed on to others via
contaminated fingernails, close contact, aerosolization, or bed linens. Once ingested,
eggs will hatch in the duodenum and begin to mature in the bowel. Adult male and
female worms mate in the terminal ileum, cecum, and appendix area. The male
worm typically dies in the cecum and is passed out with stooling. The female worm
migrates to the perianal area to lay eggs and die. The circle of life is completed!
Each female produces an average of 10,000 eggs.
Geographic Regions Affected: Worldwide. Pinworms are the most common helminth infection in the United States
and Western Europe.
Description: Pinworms is a human nematode infection caused by the ingestion of eggs from
the perianal area of infected individuals. Anal itching (pruritus ani) and scratching
aids transmission. The disease is most common in children between ages of 5 and
10 years of age.
Signs and Symptoms: Most infections are asymptomatic. Pruritus ani is the most common symptom and is
worse at night.
Diagnostic Testing: “Scotch tape test” or paddle test revealing the presence of eggs is diagnostic. In this
test, an adhesive tape or paddle is placed on several spots around the perianal area,
removing eggs that are identified on microscopy. Samples should be taken over
several days, preferably first thing in the morning. Eggs are translucent, bean shaped,
and measure 50–60 3 20–30 mm.
Pearls: Humans are the only animals that get infected, but household pets may carry the
eggs on their fur. The female carries the eggs to the perianal area to expose them
to a more oxygen-enriched environment. Eggs can live for up to 3 weeks.
112
CHAPTER 45 PINWORMS
Pinworms
ROUNDWORMS
(Enterobiasis) iu s vermi
ob c
ul
er
ar i s
Ent
Ne
matode
inth
H elm n
#1 ection i rope
Inf Eu
e stern
A, W
US
113
PART 5 WORMS
The Story of Us
ROUNDWORMS
8-13mm
long 0.5
mm
0.2
mm
Translucent eggs
50-60um x 20-30um
Female:
pointed
Male: end
rounded 2-5mm
end long
114
CHAPTER 45 PINWORMS
ROUNDWORMS
the story begins.
2 Eggs hatch in
the duodenum.
4 Worms fall in
love and mate. 3 Worms mature
in the bowel.
Hakuna Matata!
5 Male dies.
115
PART 5 WORMS
Lifecycle: The disease is contracted from exposure to fecal contaminated soil. Filariform larvae
mature and enter through exposed skin, usually the feet. From here they migrate
hematogenously to the lungs where they are coughed up and swallowed. The larvae
penetrate the mucosa of the small intestine where they mature and reproduce. Adult
N. americanus worms can live up to 5 years, while A. duodenale lives for about 6 months.
Eggs (rhabditiform larvae) are produced and they are excreted with feces. Immature
larvae are excreted and mature to filariform larvae to infect others. While both filariform
larvae can infect humans by penetrating the skin, A. duodenale can cause infection if
ingested.
Geographic Regions Affected: Worldwide, now uncommon in United States. N. americanus: North and South
America, sub-Saharan Africa, Southeast Asia, China. A. duodenale: Middle East,
North Africa, India. Annual rainfall of 50–60 inches is required for regions to
support hookworm.
Description: Hookworm is a nematode infection of the human gastrointestinal (GI) tract that
causes intestinal inflammation leading to iron-deficient anemia and protein
deficiency.
Signs and Symptoms: Mild infections are often asymptomatic. Acute infections may present with “ground
itch” and GI symptoms including nausea, vomiting, and diarrhea. Chronic infection
causes iron and protein deficiency secondary to blood loss from the feeding worms.
Diagnostic Testing: Lab tests may reveal eosinophila and microcytic anemia. Serial stool samples
are diagnostic. It should be noted that the eggs from the two species are
indistinguishable.
116
CHAPTER 46 HOOKWORM
ROUNDWORMS
os r ameri d
to c
Neca yl
en n u s
Anc
a
ale
7–13 mm
Ne
matode
I look like
an 80s horror
movie monster!
117
PART 5 WORMS
Synonym: Trichuriasis
Lifecycle: Immature eggs are passed in the feces to soil where they embryonate for 2–4 weeks
before becoming infectious. Infectious eggs can be consumed by poor handwashing
and sanitation or through ingestion on unwashed vegetables, particularly where
human waste is used as fertilizer. Once ingested eggs hatch in the small intestine, the
larvae mature and migrate to the cecum and ascending colon where they attached
after 2–3 months; 7000–20,000 eggs are released per day, per female worm, and
are not infectious until a 2- to 4-week embryonation process is completed in warm,
moist soil.
Signs and Symptoms: Most infections are asymptomatic unless there is significant worm burden. Moderate
infections cause loose stool and nocturnal stooling. Severe infections can have worms
extending to the rectum and can cause rectal prolapse or colitis.
Diagnostic Testing: Eosinophilia may be present on labs. Stool samples 33 to identify eggs.
Pearls: Coinfection with ascariasis is not uncommon, since both worms have similar
geographic distribution and patterns of infection.
118
CHAPTER 47 WHIPWORM
Whipworm ur is trichi
ROUNDWORMS
ich u
ra
Tr
(Trichuriasis)
4 cm
Ne
matode
7000–20,000
Eggs/Day
Females
Larger
Head Burrows
into Mucosa
Synonym: Trichinellosis
Lifecycle: In humans, the disease is typically acquired from the ingestion of undercooked pork
or bear meat containing Trichinella cysts. When exposed to gastric acid, these cysts
release larvae that burrow into the mucosa of the small intestines. Here the larvae
mature and reproduce. After a week, the adult females release newborn larvae that
travel through the blood stream, infect striated muscle tissue and form new cysts.
Adult worms typically survive for 4 to 6 weeks in the host gastrointestinal (GI) tract
before dying off and passing with stool. Meanwhile, encysted larvae can survive in
muscle tissue for many years, and the lifecycle repeats itself when infected meat
is consumed. Humans, barring cannibalism, are dead-end hosts. Other animals,
including rats, foxes, wild boars, and cats, can also become infected. In domesticated
pigs the cycle is perpetuated when they are fed infected meat scraps, perform
cannibalism, or consume infected rodents.
Geographic Regions Affected: Worldwide. It is uncommon in the U.S. but endemic in Japan and China.
Description: Trichinosis is a nematode infection of the human GI tract in which the parasites’
larvae ultimately form cysts in muscle tissue. Symptoms are based on the number
of cysts ingested.
Signs and Symptoms: Mild infections are often asymptomatic or mild. Significant infections, seen after
an ingestion of meat containing numerous cysts, present with two distinct stages.
Intestinal Stage: Symptoms begin as early as 2-7 days after exposure and are related
to the larvae burrowing into the GI mucosa. Symptoms can include abdominal pain,
nausea, vomiting, and diarrhea. Muscle Stage: These symptoms typically occur
10 days after infection and are more profound. Symptoms represent the newly formed
larvae infecting muscle tissue and include fever, severe muscle pain, swelling,
weakness, fever, periorbital edema, and splinter hemorrhages. Myocarditis occurs
rarely but is the most-frequent cause of death. The formation of cysts in the
diaphragm muscles can potentially compromise breathing and respiration.
Diagnostic Testing: Labs will reveal leukocytosis, eosinophilia, and increased creatine phosphokinase
(CPK). ELISA testing can be used to detect IgG antibodies to trichinella, and
confirmatory diagnosis is made via muscle biopsy. Eosinophilia doesn’t correspond
to disease severity.
Treatments: Albendazole or mebendazole combined with oral prednisone is effective for treatment.
120
CHAPTER 48 TRICHINOSIS
Trichinosis
ROUNDWORMS
in ella spir
ch a
(Trichinellosis)
Tri
lis
Ne
matode
Ingestion of Bear
Undercooked Meat
Larvae penetrate GI
mucosa, mature
and mate.
Undercooked
Meat
Newborn larvae
spread via blood
to form new cysts
Instestinal Stage Muscle Stage
in muscle.
Abdominal Pain Muscle Pain/Swelling
Nausea/Vomiting Weakness/Fever
Diarrhea Periorbital Edema
Cough/dyspnea
121
PART 5 WORMS
Lifecycle: The disease is contracted from the ingestion of unfiltered water that contains copepods
or “water fleas” hosting mature, infectious larvae. The ingested copepods die, releasing
larvae that then penetrate through the bowels and take up residence in the abdominal
cavity and retroperitoneal space. The worms mature over a period of 3 months, mate,
and then the male dies. The female worms begin their migration through subcutaneous
tissue to the lower extremities about 1 year after mating. Once toward the distal lower
extremities, the worms migrate more superficially, creating a papule that ultimately
ulcerates, allowing the worms to extend out of the wound and release eggs. The
ulceration is quite painful and infected individuals are inclined to dip the affected
extremity into water as a means of pain control. Once exposed to water, the worm
pokes out, releasing larvae. Small copepods then ingest the larvae, which undergo
further development inside the copepod. When infected copepods are ingested by
humans, the cycle repeats itself.
Geographic Regions Affected: Africa. However, due largely in part to efforts by the Carter Foundation, global
eradication of the Guinea worm is almost complete.
Signs and Symptoms: Initial infection is asymptomatic. About 1 year later, pregnant females will cause pain
in the lower extremities as they migrate distally (fiery serpent). Prior to penetrating
out through the skin, a severely painful papule forms that eventually ulcerates. The
formation of the papule may be associated with nausea, vomiting, diarrhea, and fever.
Diagnostic Testing: The diagnosis is made clinically and no specific diagnostic tests are required. Once
the small painful ulcer develops and the lower extremity is submerged into cool
water, the worm will reveal itself.
Treatments: Once the worm reveals itself, its distal end is wrapped around a small twig or piece of
gauze. Over the next several days, weeks, or months, the skin is massaged and the
twig is slowly rotated drawing more of the worm out being careful to not break the
worm. Topical antibiotics may be used to prevent superimposed infections.
Prevention: Proper water filtration using fine cloths or bio-sand filters to remove copepods. Water
can also be boiled. Insecticides like temefos can be added to water supplies to kill off
water fleas and copepods.
Pearls: When the male worms die they are absorbed by the hosts. Female worms can be
quite long, measuring 2 mm wide by 60–100 cm long. Care must be taken to avoid
breaking the worm during removal, as the remaining piece can putrefy and cause skin
necrosis along the tract. These worms have almost been eradicated from existence
and have plagued humans for centuries. Worms have been found in Egyptian
mummies, and some speculate that the Staff of Asclepius may represent a Guinea
worm wrapped around a small stick.
122
CHAPTER 49 DRACUNCULIASIS
ROUNDWORMS
nc
ne
cu
(Guinea Worm Disease, GWD)
nsis
Dra
Nem
atode
Disease Found in
Egyptian Mummies Boil Water
Painful
Ulcer
Larvae consumed
Larvae mature
in copepod. by copepods
(Water Fleas).
123
PART 5 WORMS
Lifecycle: The disease is contracted from cutaneous penetration of the filariform larvae of
hookworms that typically infect dogs and cats. Hookworm eggs are shed from
infected dogs or cats into sandy soil and after a 2-week period, develop into infectious
filarial larvae. If a dog or cat is exposed, the filarial larvae can penetrate its skin
and migrate into deeper tissues. In humans, these specific larvae lack the necessary
enzymes to penetrate through the basement membrane to enter into the deeper
dermal layers and cannot complete their lifecycle.
Geographic Regions Affected: Worldwide, more frequent in tropical and subtropical nations of Southeast Asia,
Africa, South America, Southeastern United States, and the Caribbean.
Signs and Symptoms: Patients will develop red and intensely pruritic serpiginous tracks on their lower
extremities. Itching may cause secondary bacterial infections. The condition is
self-limiting and oral anti-helminthic agents will quickly abate symptoms.
Diagnostic Testing: Eosinophilia may be seen on labs. The diagnosis is typically made with clinical
history and classic presentation.
Prevention: Wear sandals, deworming of dogs and cats, proper disposal of pet feces.
Pearls: “Ground itch” can also be seen with human hookworm and threadworm infections.
The cutaneous manifestations of threadworm (Strongyloides stercoralis) is referred to
as larva currens and is differentiated by its rapid migration, perianal involvement,
and wide band of urticaria.
124
CHAPTER 50 CUTANEOUS LARVA MIGRANS
ROUNDWORMS
(CLM/Creeping Eruption)
(Sandworms) toma brazi
os
lie
yl
(Plumber’s Itch)
Anc
nse
(Ground Itch)
Ne
matode
I think we infected a
human! We can only
proceed in dogs
and cats!
125
PART 5 WORMS
Synonym: Strongyloidiasis
Lifecycle: The disease is contracted from exposure to fecal-contaminated soil. Filariform larvae
mature and enter through exposed skin, usually the feet. From there they migrate
hematogenously to the lungs, where they are coughed up and swallowed. The larvae
penetrate the mucosa of the duodenum and jejunum, where they mature and
reproduce. Adult worms can live up to 5 years. Eggs (rhabditiform larvae) are
produced and they are excreted with feces. Autoinfection can occur when larvae
mature in the gastrointestinal (GI) tract and penetrate the colonic or anal mucosa.
Immature larvae are excreted and mature to filariform larvae to infect others.
Geographic Regions Affected: Tropical and subtropical areas of the world with poor sanitation; Vietnam, Cambodia,
Laos, some parts of Africa, Brazil, and Central America.
Signs and Symptoms: Most immunocompetent adults are asymptomatic. Cutaneous symptoms can include
pruritus, burning, edema, and inflammation at the site of infection. Pulmonary
symptoms may include cough, dyspnea, hemoptysis, and a Loffler-like syndrome.
GI symptoms include epigastric pain, nausea, vomiting, and diarrhea. Hyperinfection
syndrome: Immunocompromised patients may suffer from autoinfection and develop
significant worm burden. Fever, severe nausea, vomiting, abdominal pain, and
pulmonary symptoms would manifest, potentially leading to multisystem organ
failure, sepsis, shock, and death.
Diagnostic Testing: Identification of rhabditiform larvae in stool samples. Up to three stool samples
are usually required and specialized techniques, such as the agar plate method,
increase sensitivity. Using the agar plate method, plates are inoculated with stool
and incubated for 2 days. Larvae will migrate from the stool, creating bacterial trails
along the way. If negative, a string test can be performed. Here the patient swallows
a capsule attached to a long string and when removed, the string is tested for larvae.
IgM/IgG serology can also be obtained.
Treatments: Ivermectin is the preferred treatment. Albendazole can be used as an alternative, but
it is less effective. For hyperinfections, treatment needs to be repeated after 15 days.
126
CHAPTER 51 THREADWORM
ROUNDWORMS
gy
or
(Strongyloidiasis)
Stro
a li s
Ne
matode
Nausea
Vomiting
Cough
Wheezing
Hemoptysis
(2) Larvae are coughed
up and swallowed.
Rhabditiform
Larvae
(Noninfectious)
127
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2
PART 5
Section
TAPEWORMS
PART 5 WORMS
Lifecycle: Pork tapeworm disease is contracted from ingestion of infected “measly” pork
containing cysticerci. Once inside the human intestine, the cysts hatch, releasing
protoscolices that attach to the intestinal wall, becoming the heads (scolex) of
adult tapeworms. Hermaphroditic proglottids form off the scolex, mature, become
pregnant, produce eggs, and eventually break off the tapeworm. Degraded
proglottids release eggs into the passed stools. Contaminated human feces are
consumed by pigs, the eggs hatch in their gastrointestinal (GI) tract, and then
the larvae seek out striated muscle, forming cysticerci. Humans can serve as
intermediate hosts if they consume Taenia solium eggs through fecal contamination
or autoinoculation. This could cause the more-severe condition cysticercosis, the
development of cysticerci in human muscle or brain tissue (neurocysticercosis).
Geographic Regions Affected: Worldwide. Common in places where humans live in close contact with pigs and
could eat undercooked pork: Central and South America, India, and Asia.
Description: Pork tapeworm is a cestode infection of the human GI tract, which is often
TAPEWORMS
Signs and Symptoms: Pork tapeworm is often asymptomatic. Significant worm burden may cause nausea,
abdominal discomfort, and malaise. Cysticercosis may remain asymptomatic for years
until the cysts degrade and activate the host’s immune system. Neurocysticercosis can
present as altered mental status, seizures, or symptoms associated with hydrocephalus
such as headache, nausea, and blurred vision.
Diagnostic Testing: Serial stool samples looking for eggs is diagnostic for tapeworm, and serologic
testing can be a useful adjunct. CT or MRI neuroimaging is necessary for the
evaluation and diagnosis of neurocysticercosis.
Prevention: Sanitation and proper hygiene, proper cooking of pork, and/or freezing pork to
215°C for at least 20 days. Pickling pork does not kill the cysticerci.
Pearls: Humans are the only definitive host for Taenia solium and pigs or humans serve as
intermediate hosts. Worms measure 2–8 m in length on average, have hooks on their
scolex, live for several years, and produce eggs that can survive for about 2 months in
the environment.
130
CHAPTER 52 PORK TAPEWORM AND CYSTICERCOSIS
Pork Tapeworm Ta
en ia solium
2–8 meters
Cestode
Cysticerci
in Brain
(Measly) Cysticerci
Hooks
Undercooked in Eyes
uces tapeworm
Pork prod
Scolex
TAPEWORMS
is os
I’ve got
Cysticerc
Dope Hooks!
Proglottid
Hermaphrodite
stion
Egg Inge
Cysticerci
Develops
lation or
in Muscle
Cysticerci
in Muscle
u
Autoinoc
Ovum (Eggs)
in Feces
131
PART 5 WORMS
Lifecycle: Broad fish tapeworm disease is contracted from the ingestion of infected undercooked
fish. Once ingested, plerocercoids develop into adult worms and attach themselves
to the lining of the small intestine. Reproduction is asexual, as the worm is a
hermaphrodite. When mature, pregnant proglottids release eggs into the stool.
Immature eggs develop into embryos in fresh water and become coracidium. These
coracidium are consumed by small crustaceans/copepods (first intermediate host)
and develop into proceroid larvae. Copepods are then consumed by small fish like
minnows (second intermediate host) and the proceroids infect the fish and develop
into pleroceroid larvae. Many of these small fish are consumed by larger predator fish.
Humans (definitive host) are infected by the ingestion of the undercooked small fish
or larger predator fish (most common). Once in the human, the pleroceroid develops
into adult worms and the cycle is repeated.
Description: Broad fish tapeworm is a cestode infection of the human gastrointestinal tract,
TAPEWORMS
which is often asymptomatic. The disease is contracted via the ingestion of raw or
undercooked fish. Common dishes include sushi, sashimi, and ceviche.
Signs and Symptoms: Often asymptomatic. Significant worm burden may cause nausea, vomiting, abdominal
discomfort, diarrhea, and malaise. After years of infection, human hosts may develop
B12 megaloblastic anemia. This is because the worm consumes most of the host’s
ingested B12—the worm essentially steals it!
Diagnostic Testing: Serial stool samples looking for eggs and proglottids are diagnostic. Long-term
infections can cause B12 deficiency anemia, sometimes quite significant, presenting
with neurologic findings.
Treatments: Praziquantel and niclosamide are effective treatment options. Vitamin B12
supplementation may be necessary to treat anemia.
Pearls: Worms measure 10–25 m in length on average and are the largest tapeworms to
infect humans. Their bodies have a unique scolex with two ventral grooves used to
attach to the intestinal wall, a neck, and proglottids that are wider than they are long.
Canines, felines, and bears can also serve as definitive hosts.
132
CHAPTER 53 BROAD FISH TAPEWORM
at
Diph
um
Half price
sushi! 10–25 meters
Cestode
Scolex
I steal all
your B12!
Neck
Proglottid
TAPEWORMS
(Width>Length)
Ceviche
Predator Fish
Pleroceroid
Fish
Embryos
Eggs
Copepods
Coracidium
Proceroid
133
PART 5 WORMS
Lifecycle: Beef tapeworm disease is contracted from ingestion of infected “measly” beef
containing cysticerci. Once inside the human intestine, the cysts hatch, releasing
protoscolices that attach to the intestinal wall, becoming the heads (scolex) of adult
tapeworms. Hermaphroditic proglottids form off the scolex, mature, become pregnant,
produce eggs, and eventually break off the tapeworm. Degraded proglottids release
eggs into the passed stools. Contaminated human feces are consumed by cattle, the
eggs hatch in their gastrointestinal (GI) tract, and then the larvae seek out striated
muscle, liver, and/or lung tissue to form cysticerci. Unlike the pork tapeworm,
humans cannot serve as intermediate hosts for beef tapeworm.
Geographic Regions Affected: Worldwide. Common in Central and South America, Europe, Africa, and Asia.
Description: Beef tapeworm is a cestode infection of the human GI tract, which is often
asymptomatic.
Signs and Symptoms: Often asymptomatic. Significant worm burden may cause nausea, abdominal
TAPEWORMS
Diagnostic Testing: Serial stool samples looking for eggs are diagnostic for tapeworms. Taenia (beef and
pork tapeworm) eggs cannot be distinguished morphologically, but their proglottids
have different appearances under microscopy. India ink staining highlights the
ovaries and testicles of the proglottids.
Prevention: Sanitation and proper hygiene, proper cooking of beef, and/or deep-freezing beef
long enough to kill cysticerci.
Pearls: Humans are the only definitive host for T. saginata, and cattle serve as intermediate
hosts. Worms measure 4–12 m in length on average, but they can be larger. Beef
tapeworms are larger than pork tapeworms, and their scolex has four suckers and
lacks hooks. Worms can live for several years and produce eggs that survive for
about 2 months in the environment.
134
CHAPTER 54 BEEF TAPEWORM
Beef Tapeworm ae
nia sagina
t
a
4–12 Meters
Cestode
Where’s the
Here
beef tapeworm?
Malaise I am! No Hooks
(Measly) Scolex
Undercooked
Beef Proglottid
Hermaphrodite
TAPEWORMS
Abdominal
Cramping
Cysticerci
Muscle
Liver
Lungs
Ovum (Eggs)
in Feces
135
PART 5 WORMS
Lifecycle: E. granulosus causes cystic echinococcosis (AKA: hydatid disease); mature worms
in definitive hosts (dogs) release infectious eggs, which are consumed by
incidental (human) or intermediate hosts (sheep, cattle, goats, horses, camels,
swine). E. multilocularis causes alveolar echinococcosis; mature worms in
definitive hosts (foxes, coyotes) release infectious eggs, which are consumed by
incidental (human) or intermediate hosts (rodents).
Geographic Regions Affected: E. granulosus (CE): South and Central America, Middle East. E. multilocularis (AE):
North America, Western China, Russia.
Signs and Symptoms: Cystic echinococcosis (CE): Initial infection is asymptomatic and might not cause
TAPEWORMS
symptoms for decades. Cysts are often singular and affect one organ, most commonly
the liver (50%–70%) or lung (20%–30%). CNS, renal, and bone cysts can also occur.
Cysts will enlarge over time, causing pain and symptoms in their respective organ
systems. Many patients remain asymptomatic for their lifetime, with disease discovered
incidentally at autopsy. Ruptured cysts may cause anaphylaxis. Alveolar echinococcosis
(AE): The vast majority of cysts (.99%) are hepatic and symptomatic. Symptoms are
vague and include fatigue, malaise, and right upper quadrant pain from liver capsule
enlargement. If untreated, the mortality rate is high.
Diagnostic Testing: Diagnostic imaging including CT scan, MRI, and ultrasound can be used to locate
and visualize cysts. After cyst detection, serology can confirm the diagnosis. ELISA
serology for antibody detection is more sensitive than serology for antigen detection.
Pearls: To associate respective intermediate and definitive host relationships, remember that
dogs herd cattle and sheep, while foxes and coyotes eat rodents.
136
CHAPTER 55 ECHINOCOCCOSIS
Echinococcosis s
occu gran
oc
ul
n
osu
Echi
s
laris
Echi
Definative Hosts Cestode
cu
no
co o
ccus multil
AE
CE
Ingestion of
Cysts Ingestion of Eggs
(Organs) (Feces)
TAPEWORMS
Brain
UNCOMMON
Lung
20%–30% CE
Heart
Kidney
Intermediate Hosts Liver
50%–70% CE Bone
99% AE
137
PART 5 WORMS
Lifecycle: The disease is contracted from the ingestion of infected insects (beetles and
mealworms) serving as intermediate hosts or by the direct ingestion of eggs in
contaminated soil, food, or water. The ingested eggs release oncospheres that
penetrate the intestine villus and form cystircercoid larvae. These larvae then develop
into adult tapeworms and attach to the lining of the ileum. Eggs are produced and
released into passing stool. Since eggs are infectious without further development,
autoinoculation can occur. The dwarf tapeworm is unique because it can complete its
entire lifecycle in the human or with the assistance of small arthropods serving as the
intermediate hosts.
Geographic Regions Affected: Worldwide. Common in Egypt, Sudan, Thailand, India, and South America.
Description: Dwarf tapeworm is an infection of the human gastrointestinal tract, which is often
asymptomatic.
Signs and Symptoms: Often asymptomatic. Significant infections are more common in children and may
TAPEWORMS
Diagnostic Testing: Serial stool samples looking for eggs are diagnostic.
Pearls: Eosinophilia is common. Chronic infection can have a profound impact on pregnant
women and causes growth retardation in young children. Rodents that consume
infected beetles or meal worms (intermediate hosts) can also serve as definitive hosts
for this parasite.
138
CHAPTER 56 DWARF TAPEWORM
Dwarf Tapeworm
nolepis na
me
Hy
na
Infects humans
and rodents!
Ce s to de
I’m only 2
inches long!
TAPEWORMS
Rodent
Insect eats
eggs.
Water
Food
Soil
139
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3
PART 5
Section
FLATWORMS
PART 5 WORMS
Lifecycle: The disease is contracted via the penetration of schistosoma cercariae through
exposed skin when wading or bathing in fresh, slow flowing, snail-infested water.
Eggs are passed through infected human feces (S. japonicum, S. mansoni) or urine
(S. haematobium). Once in fresh water, eggs hatch and release miracidia that penetrate
specific snails (intermediate host). Once in the snail, miracidia reproduce asexually
over the next 4–6 weeks and mature into cercariae. When cercariae are released from
the snail, they seek out a definitive host. Once penetrating the human skin, miracidia
transform to schistosomula and migrate to the lungs, where they mature over the
next 5–6 weeks before descending into their respective venous environments. The
worms reproduce sexually and release eggs into human feces or urine, depending on
species. Adult worms live an average of 3–5 years.
Geographic Regions Affected: Africa and Middle East (S. haematobium); China, Thailand, Indonesia (S. japonicum);
South America, Africa, Caribbean (S. mansoni)
Signs and Symptoms: Most infections are asymptomatic, with severity of illness based on worm burden.
“Swimmers itch” or schistosome dermatitis occurs when the cercariae penetrate
the skin and cause urticaria, pruritus, and a macular rash. Previously sensitized
individuals may have more pronounced symptoms. Acute schistosomiasis may cause
Katayama fever, specifically from S. japonicum and S. mansoni. Several weeks after
exposure, patients may develop fever, chills, malaise, abdominal pain, diarrhea,
hematochezia, chest pain, cough, and hepatosplenomegaly. Chronic infections can
cause granulomatous changes in the liver (S. japonicum, S. mansoni) and hematuria
(S. haematobium). S. haematobium can cause bladder calcification and ureteral
reflux, leading to kidney damage.
Diagnostic Testing: Labs will reveal eosinophilia. Serial stool and urine samples are required to identify
the excreted eggs. Urine antigen testing is available in some countries.
Pearls: Respective species can increase incidence of hepatocellular (S. japonicum, S. mansoni)
and bladder cancer (S. haematobium).
142
CHAPTER 57 SCHISTOSOMIASIS
Schistosomiasis
(Snail Fever) o o d Fl u k
Bl
e
S. haematobium
S. japonicum
S. mansoni
Fatique
Malaise
Cough
BioSand
Filter Fever
Abdominal
Hepatosplenomegaly Pain
Hematuria
Diarrhea (Red)
FLATWORMS
(Swimmer’s Itch)
Rash
Cercariae
143
PART 5 WORMS
Lifecycle: The disease is contracted from ingestion of undercooked fish. From infected humans,
embryonated eggs are passed into the environment through feces. The eggs are
consumed by specific snails (first intermediate host), wherein they hatch to form
miracidia. The miracidia reproduce inside the snail and produce large numbers of
cercariae. The cercariae are eventually released into the water and penetrate fish
(second intermediate host), wherein they form metacercarial cysts. Once humans
ingest the undercooked fish, metacercarial cysts hatch, migrate through the upper
GI tract, and take up residence in the gallbladder and bile ducts. There they feed on
bile, reproduce, and can live for up to 30 years.
Geographic Regions Affected: East and Southeast Asia (C. sinensis), Southeast Asia (O. viverrini), Russia (O. felineus)
Description: The Chinese liver fluke is a trematode infection of humans with preference for the
bile ducts and gallbladder.
Signs and Symptoms: Patients may initially be asymptomatic or develop fever, nausea, vomiting, diarrhea,
and abdominal pain within 4 weeks of initial infection. Chronic symptoms are
associated with worm burden and feeding within the bile ducts and include right
upper quadrant pain, jaundice, elevated liver enzymes, malaise, and weight loss.
Long-standing infections can cause periductal fibrosis and increased incidence of
biliary ductal carcinoma.
Diagnostic Testing: Labs will reveal eosinophilia, elevated liver enzymes, and increased bilirubin levels.
Eggs can be identified in serial stool samples, duodenal aspirates, or bile specimens.
Diagnostic imaging including US, CT, and MRI will reveal biliary ductal dilation and
wall thickening. Worms may be visualized swimming in the gallbladder on US.
Pearls: Chronic infection increases the likelihood of developing biliary duct and gallbladder
carcinoma.
FLATWORMS
144
CHAPTER 58 LIVER FLUKE
rri sis
Clon i
Op
(Chinese Liver Fluke)
en
ni
Trematode
Op
s
eu
st i n
ho
rc hi s fel
i
Definative Host
(Humans)
Causes
Cancer! Human ingests
undercooked fish.
Metacercarial
Fluke lives in cysts form
gallbladder and in fish.
bile ducts.
Cercariae
penetrate fish. 2nd
Intermediate
Miracidia
Host
FLATWORMS
mature to
cercariae.
1st
Intermediate
Host
Eggs ingested
by snail.
Eggs
145
PART 5 WORMS
Lifecycle: The disease is contracted from the ingestion of undercooked crabs (crayfish in the
United States). Starting in the definitive host (humans), unembryonated eggs are
coughed up from the lungs and excreted in the sputum or swallowed and pass with
stool. Once in the external environment, the eggs become embryonated and hatch
into miracidia. Next the miracidia find and penetrate small snails (first intermediate
host). In the snails, further development occurs over the next 3–5 months until the
snail releases cercariae. The cercariae penetrate small crabs and crayfish (second
intermediate host), wherein they form metacercarial cysts. Once humans ingest the
undercooked crustacean, metacercarial cysts hatch, penetrate through the duodenum,
and ultimately migrate to the lungs through the diaphragm, where they encapsulate
and begin egg production. Worms can live in humans for up to 20 years.
Geographic Regions Affected: East Asia (P. westermani), South America (P. mexicanus), and North America
(P. kellicotti)
Description: Paragonimiasis is a trematode infection of humans with preference for the lungs.
Signs and Symptoms: Symptoms of acute infection occur within 2 weeks and include abdominal pain
and diarrhea, followed by fever, chills, cough, and urticaria. Chronic symptoms
are associated with the shedding of eggs into the bronchial tree and include cough,
pleuritic chest pain, and hemoptysis.
Diagnostic Testing: Labs will reveal eosinophilia. Serial stool and sputum samples are required to
identify the excreted eggs. Serology and enzyme immunoassay testing are available.
146
CHAPTER 59 LUNG FLUKE
rm
g
(Paragonimiasis)
Para
ani
(Japanese Lung Fluke)
(Oriental Lung Fluke) Other species
Tr e
matode
Human ingests
undercooked crab.
2nd
Intermediate
Host
Metacercarial
cysts form
in crab.
Cercariae
penetrate crab.
FLATWORMS
1st
Eggs Miracidia
Intermediate
penetrate snail.
Host
147
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PART 6
FUNGAL
PART 6 FUNGAL
Geographic Regions Affected: Worldwide, more common in tropical and subtropical locales.
Signs and Symptoms: Cutaneous sporotrichosis is the most-common disease manifestation and typically
presents as a small, painless, nodular lesion on the finger, hand, or arm, which
eventually ulcerates. Lymphocutaneous sporotrichosis occurs as the infection
spreads up the lymph channels and secondary lesions occur and eventually ulcerate
as well. Lesions may wax and wane over months to years if left untreated. Primary
pulmonary sporotrichosis is a rare disease caused by the inhalation of spores.
Patients present with cough, mediastinal lymphadenopathy, pulmonary fibrosis,
lung nodules and cavitations. Disseminated disease can occur via hematogenous
spreading of the disease to the joints (osteoarticular sporotrichosis—most common),
lung (secondary pulmonary sporotrichosis), or central nervous system (CNS)
(sporotrichosis meningitis). Multifocal disseminated disease can occur in the
immunocompromised.
Diagnostic Testing: The diagnosis should be considered based on occupational exposure and disease
pattern or presentation. Fungal culture is the gold standard for diagnosis, and
samples should be obtained from several sites. Pathologic examination of biopsied
lesions will reveal a pyogranulomatous response and the classic “cigar body”–shaped
yeast.
Treatments: Itraconazole is the treatment of choice in most cases, except for pregnancy and
severe infections. Severe pulmonary, disseminated, or CNS infections should be
treated with amphotericin B followed by itraconazole. Alternative treatments include
saturated solution of potassium iodide or terbinafine.
Pearls: When seen under microscopy, the mold has a “daisy wheel” appearance and the yeast
has a “cigar body” shape. Dimorphic fungi grow as a “Mold in the Cold and a Yeast
in the Beast (Heat).”
150
CHAPTER 60 SPOROTRICHOSIS
Sporotrichosis
hrix sch
(Rose Gardener’s Disease) ot
en
r
Spo
k ii
m
Di
Incubation: 1–12 Weeks orp
gi
Average: 3 Weeks hic Fun
Sporotrichosis Meningitis
(Disseminated) “Every Thorn has its Sporothrix”
Lymphocutaneous
Pulmonary
(Spore Inhalation = Rare)
I can catch
Cutaneous and spread
the infection!
Osteoarticular
(Disseminated)
Daisy Wheel
Cigar Body
Hay
Mold
Geographic Regions Affected: Central and South America. Most cases have been reported in Brazil.
Signs and Symptoms: The acute or subacute disease manifestations are more common in younger patients
and the immunocompromised. The acute form presents as a significant illness with
fever, chills, malaise, weight loss, lymphadenopathy, hepatosplenomegaly, cough,
dyspnea, and multiple skin and mucocutaneous lesions. Chronic disease causes
cough and pulmonary fibrosis or emphysematous changes, chronic ulcers of the
mucous membranes, mouth, nasopharynx, or larynx, cervical lymphadenopathy, and
cutaneous skin lesions. Adrenal insufficiency is also common in the chronic setting.
Diagnostic Testing: Direct microscopy of sputum, skin lesions, lymph node aspirates or tissues using
KOH prep or calcofluor stains will often reveal yeast with a “pilot’s wheel” of “Mickey
Mouse head” appearance. Fungal cultures can be prepared from sputum or lymph
node aspirates. Serologic tests can aid in diagnosis and titers can be followed to assess
treatment response. Chest radiographs often show fibrosis and emphysematous
changes in chronic disease.
152
CHAPTER 61 PARACOCCIDIOIDOMYCOSIS
Paracoccidioidomycosis Paracoccidioides
brasiliensis
(South American Blastomycosis)
Dimorphic Fungi
Incubation :
1 month—9 Years 25ºC 37ºC
Paracoccidioides
5%–10%: Acute/Subacute lutzii
or “Juvenile” = Rapid
90%: Chronic or
“Adult” = Insidious Chills
Fever
Mucocutaneous
Lesions
Cervical
Emphysema/ Lymphadenopathy
Pulmonary
Cough
Fibrosis
(Chronic)
Hepatosplenomegaly
Weight Loss
153
PART 6 FUNGAL
Geographic Regions Affected: Desert regions in the western hemisphere, most commonly in the United States and
parts of Mexico. The two U.S. states with the most cases are Arizona and California.
Other states include Nevada, New Mexico, Utah, and Texas.
Signs and Symptoms: More than half of all infections are asymptomatic or mild. In those that are
symptomatic, acute infection often mimics community-acquired pneumonia and
symptoms can include fever, chills, malaise, headache, chest pain, cough, shortness
of breath, migratory arthralgia, myalgia, rash, and erythema nodosum. The disease
is often self-limiting after several weeks, but fatigue can persist for months. More
severe disease is often seen in the immunocompromised and/or those with a large
arthroconidial inoculum. About 5% of infections become chronic, exemplified by
severe pulmonary manifestations and/or disseminated disease with meningeal, bone,
or joint space involvement. Desert rheumatism is the triad of arthralgia, fever, and
erythema nodosum.
Diagnostic Testing: IgM/IgG serology can be obtained. Sputum samples can be sent for fungal
culture and direct examination microscopy using KOH or calcofluor staining.
For patients with early infection, isolating the organism in culture may be the
only way to diagnose since antibodies take weeks to months to develop. Titers
determined by complement-fixing antibody tests can be obtained to confirm
diagnosis and anticipate likelihood of extrapulmonary dissemination (titers 1:16
indicate a high likelihood of dissemination). Chest x-ray findings in chronic
disease can include mediastinal lymphadenopathy, nodules, granulomas, and
cavitary lesions. Spontaneous pneumothorax may occur if cavitary lesions or blebs
rupture. These findings may mimic tuberculosis (TB) or cancer.
Treatments: Mild infections are often self-limiting and resolve spontaneously. Indications
for treatment proposed by the Infectious Disease Society of America include
.10% weight loss, night sweats .3 weeks, significant pulmonary infiltrates, prominent
hilar lymphadenopathy, titers 1:16, inability to work, and/or symptoms longer than
2 months. Itraconazole and fluconazole are effective treatments for mild to moderate
disease. Amphoteracin B is recommended for severe infections or disseminated
disease.
154
CHAPTER 62 COCCIDIOIDOMYCOSIS
Coccidioidomycosis Coccidioides
Coccidioides immitis
posadasii
(San Joaquin Valley Fever)
Inhaled
Arthroconidia Meningitis Chills
Dust Storm Fever
Cough Myalgia
Pneumothorax Chest Pain
Cavitary Lesion
Mediastinal
Nodule/Granuloma Lymphadenopathy
(Often Mistaken for Cancer)
Bronchitis Shortness
Pneumonia of Breath
#1
AZ
I knew I should've
taken that left turn #2
CA
at Albuquerque!
Arthralgia
Erythema
Nodosum
155
PART 6 FUNGAL
Geographic Regions Affected: Predominantly found in the Ohio, Mississippi, and St. Lawrence River Valleys, as
well as the Great Lakes Region of the United States.
Signs and Symptoms: Up to 50% of cases are asymptomatic. When symptomatic, blastomycosis can
present in a variety of ways in the acute and chronic settings. From a pulmonary
perspective, it can present as mild flu-like illness, pneumonia, or acute respiratory
distress syndrome (ARDS). Chronic pulmonary manifestations on chest x-ray can
include nodules, granulomas, mediastinal lymphadenopathy, or cavitary lesions,
all potentially mimicking tuberculosis (TB) or cancer. Since blastomycosis is an
insidious and often slowly progressive disease, dissemination is not uncommon,
specifically in the immunocompromised. Disseminated disease can present
cutaneously as verrucous or ulcerative skin lesions, as osteomyelitis in the bones,
as disseminated lesions in the genitourinary system, or as meningitis-causing
lesions in the central nervous system (CNS).
Diagnostic Testing: Fungal culture is the gold standard for the diagnosis of blastomycosis. Direct
microscopy can detect yeast in biopsied tissues and respiratory secretions. Enzyme
immunoassay (EIA) antigen detection studies can be performed on urine, serum,
and bronchoalveolar washings. Serologic testing is not useful for the diagnosis of
blastomycosis.
Treatments: The authors recommend consultation with the Infectious Disease Society of America
guidelines. Overall, the guidelines encourage the treatment of all infected individuals
to prevent disseminated disease and recommend treatment for all patients with moderate
to severe pneumonia, disseminated disease, and compromised immune systems.
Mild to moderate pulmonary and disseminated disease can be treated with oral
itraconazole. Severe disease should be treated more aggressively with amphotericin B
followed by oral itraconazole. CNS infections are treated with amphotericin B followed
by oral fluconazole, itraconazole, or voriconazole, often for a 12-month duration.
Pearls: Under microscopy, the hyphae branch at 90 degrees and the conidia resemble lollipops.
Untreated blastomycosis has a high mortality in the immunocompromised and in
patients who develop ARDS as a result of infection.
156
CHAPTER 63 BLASTOMYCOSIS
Blastomyces
Blastomycosis dermatitidis
(Gilchrist’s Disease) Lollipops
Not Contagious
Immunocompromised = Headache
Worse Infection
Meningitis
Inhaled
Conidia
Myalgia
Cough
Chills Pleuritic
Fever Cavitary Lesion Chest Pain
(Rare)
Mediastinal
Lymphadenopathy
Nodule/Granuloma
Shortness
Alveolar or Mass-like of Breath
I can catch Pneumonia
(Often Mistaken for Cancer)
this too!
GU Involvement
Ulcerative
Lesions Verrucous Lesions
Erythema Nodosum
Osteomyelitis
157
PART 6 FUNGAL
Geographic Regions Affected: Worldwide, predominantly found in river valleys. In the United States, most cases are
found in the Midwest and Southeastern states (Ohio and Mississippi River Valleys).
There is a positive association with this disease and cave exploration in the United
States and Central and South America.
Signs and Symptoms: The vast majority of patients (<90%) are asymptomatic or have mild disease and
don’t seek medical attention. Symptomatic patients may develop fever, chills,
headache, substernal chest pain, and nonproductive cough. Malaise, fatigue, myalgia,
arthralgia, and erythema nodosum may also occur. Patients can also develop
pericarditis, mediastinitis, and/or hepatosplenomegaly. Mediastinal lymphadenopathy
can occur, but it is uncommon (5% to 10% of patients). The disease is often self-limiting,
but moderate to severe pulmonary, disseminated, and central nervous system (CNS)
infections require antifungal treatment. More-severe disease is often seen in the
immunocompromised and/or those patients with a large conidial inoculum. About
5% of infections become chronic, exemplified by the development of pulmonary
cavitary disease with low-grade fever, cough, and dyspnea mimicking tuberculosis
(TB). Chronic cavitary disease is more common in those with preexisting emphysema.
Diagnostic Testing: Enzyme immunoassay (EIA) antigen detection studies can be performed on urine,
serum, and bronchoalveolar washings. Titers determined by complement-fixing
antibody tests can be obtained to confirm diagnosis. Fungal cultures can be performed
on respiratory secretions. Acute chest x-ray findings may reveal patchy pneumonitis
and mediastinal lymphadenopathy. Chest x-ray findings in chronic disease can include
mediastinal lymphadenopathy, nodules, granulomas, and cavitary lesions. These findings
may mimic TB or cancer.
Treatments: Mild infections are often self-limiting and resolve spontaneously. Indications and
recommendations for treatment are based on the severity of illness and the authors
recommend consultation with the Infectious Disease Society of America guidelines.
Itraconazole is effective for mild to moderate disease with symptoms lasting longer
than 1 month. Amphoteracin B is indicated for severe infections.
158
CHAPTER 64 HISTOPLASMOSIS
Histoplasmosis Histoplasma
capsulatum
(Spelunker’s Lung/Cave Disease)
Meningitis
Chills
Fever
Nodule/Granuloma Pericarditis
(Often Mistaken for Cancer) 5%
Patchy Pneumonitis
Hepatosplenomegaly
Erythema
Nodosum
Black Birds
Starlings
Arthralgia
Guano
159
PART 6 FUNGAL
Tinea Corporis (Ringworm): Fungal infection of the trunk or extremities, commonly appear as a raised, red ring
with a central clearing. The infection can be spread from person to person or
acquired as a zoonosis from dogs, cats, cattle, and other animals. The disease is more
common in hot and humid climates. Treatment is similar to that for tinea pedis.
Tinea Cruris (Jock Itch): Fungal infection of the groin and inguinal region, more common in athletic males.
Tinea cruris is often bilateral and spares the penis and scrotum. It can be distinguished
from Candida largely by the absence of satellite lesions. Treatment is similar to that for
tinea pedis.
Tinea Manuum: Fungal infection of the hand(s). Treatment is similar to that for tinea pedis.
Tinea Faciei/Tinea Barbae: Fungal infection of the face, neck, or beard area. Folliculitis, sycosis barbae, and
pseudofolliculitis barbae should be considered in the differential. Given the
involvement of numerous hair follicles, oral therapy is the preferred treatment.
Tinea Capitus: Fungal infection of the scalp characterized by pruritic, annular patches of alopecia.
The condition is most common in young children and can occur with or without
inflammation. The hair shafts in tinea capitus are infected in one of two ways. In
ectothrix infections, spores are formed on the exterior of the hair shafts and hairs
break off several millimeters above the scalp. In endothrix infections, spores are
formed within the individual hair shafts and this causes the hairs to break at the level
of the scalp, often appearing as clusters of black dots. If inflammation is significant, a
raised, boggy, soft tissue mass known as a kerion may form. Kerions are occasionally
mistaken for bacterial abscesses. Oral antifungals are required for treatment and
include griseofulvin, terbinafine, itraconazole, and fluconazole.
Tinea Fungal infection of fingernails and/or toenails. Treatment is mostly for cosmetic
Unguium/Onychomycosis: purposes, and oral medications are the most effective, including itraconazole,
fluconazole, and terbinafine. Some medications may require pulsed dosing, and
toenails typically require a longer duration of treatment than fingernails. There are
some lacquers (ciclopirox or amorolfine) available for treatment, but they have
limited effectiveness.
160
CHAPTER 65 TINEA INFECTIONS OF THE SKIN
?
here
Tinea Pedis But w
Somewhere I’ll
cause a local
infection!
Tinea Corporis
inea
My t cause
tions !
infec e itching
t e n s
in
Tinea Manuum
Tinea Barbae
Tinea Unguium
TREATMENTmiSconazole, naftifine,
azole,
inafine, clotrim lopirox
Topical: terb se le niu m sulfide, cic
tolnaftate,
ulvin,
azole, griseof
Tinea Cruris Tinea Capitis fine, clotrim
Oral: terbina ole, fluconazole
itraconaz
161
PART 6 FUNGAL
Incubation: Unknown/Varied
Geographic Regions Affected: Worldwide. More common in tropical and subtropical regions.
Description: Tinea versicolor is a cutaneous overgrowth of a common topical yeast, often more
pronounced in warm, humid environments and during the summer months.
Signs and Symptoms: Lesions have sharp boarders, are nonpruritic, and tend to affect the trunk and
proximal extremities. In lighter-skinned people, lesions may be hyperpigmented,
whereas hypopigmentation occurs more commonly in darker-skinned people.
Tanning tends to enhance the appearance of these lesions.
Diagnosis: This is typically a visual diagnosis. Microscopy with KOH preparation will reveal the
characteristic “spaghetti and meatballs” appearance of round yeasts with short
hyphae filaments. Lesions will fluoresce yellow-green under a Wood’s lamp.
Treatments: Topical azole antifungal or terbinafine creams are effective and inexpensive. Less
effective treatments include topical selenium sulfide lotion. Severe cases can be
treated with oral itraconazole, ketoconazole, or fluconazole.
Pearls: Telling an attractive young female that she has a noncontagious skin infection
does not make for a good introduction or icebreaker. This has been confirmed by
independent research on at least two separate occasions.
162
CHAPTER 66 TINEA VERSICOLOR
Tinea Versicolor
(Pityriasis Versicolor) Malassezia globosa
Malassezia furfur
s”
“S p
ag
a ll
het tb
ti and Mea
Fluoresces yellow-green
under Wood’s lamp.
163
PART 6 FUNGAL
Incubation: Unknown/Varied
Aspergilloma or A localized collection or “ball” of noninvasive Aspergillus can occur in the sinuses
“Fungus Ball”: (maxillary is most common) or in a preexisting pulmonary cavity (typically in the
apex of the lung) in patients with bullous emphysema, TB, or sarcoidosis. Treatment
is surgical.
Otomycosis: Noninvasive chronic otitis externa infection caused by Aspergillus spp. A. niger
will have a blackish coloration and/or drainage, whereas A. fumigatus will have a
greenish hue.
Invasive Pulmonary IPA is an invasive, florid Aspergillus infection of the lungs in immunocompromised
Aspergillosis (IPA): patients, typically those with significant neutropenia. Signs and symptoms include
fever, cough, dyspnea, and chest pain. Chest x-ray will reveal diffuse infiltrates and
CT scan of the chest may reveal the “halo” (ground glass appearance surrounding a
nodule) or “air crescent” signs.
Cerebral Aspergillosis: Cerebral spread of Aspergillus has an extremely high mortality and presents as
headaches, focal neurologic deficits, and altered mental status. CT scans may reveal
ring-enhancing lesions and localized edema.
164
CHAPTER 67 ASPERGILLOSIS
Aspergillosis gill
us fumi
er rgillus fla g
e
at us
Asp p
As
us
v
Fu n gi
Cerebral Aspergillosis
•Ring-Enhancing Lesion
Aspergilloma
“Fungus Ball”
•Maxillary Sinus
Otomycosis
•Preexisting Pulmonary
•A. niger
cavities in Lung Apex
Black Drainage
•A. fumigatus
Green Drainage
Allergic Bronchopulmonary
Aspergillosis (ABPA) Invasive Pulmonary
• Asthma or CF Aspergillosis
• Bronchiectasis •Immunocompromised
• Skin test / IgE •Neutropenia
• Eosinophilia •Diffuse Pulmonary Infiltrates
• Infiltrates on CXR •”Halo” Sign
•”Air-crescent” Sign
165
PART 6 FUNGAL
Causative Agents: Mucor spp., Rhizopus spp., Lichtheimia spp., Cunninghamella spp.
Incubation: Unknown/Varied
Signs and Symptoms: Rhinocerebral: Symptoms are progressive and initially consistent with sinusitis. Fever,
headache, unilateral facial swelling/pain/numbness, sinus congestion, unilateral
ocular abnormalities (blindness), and eventually, hard palate ulcerations and eschar
formation secondary to ischemic necrosis. Pulmonary: Fever, chills, cough, dyspnea,
chest pain, hemoptysis, and pulmonary infiltrates are hallmarks. Presentation may be
indistinguishable from invasive pulmonary aspergillosis. However, in pulmonary
mucormycosis, patients will often have concurrent rhinocerebral symptoms.
Cutaneous: Infection begins as an area of erythema that progresses to a black eschar.
Given the angioinvasive properties of the fungi, necrotizing fasciitis can occur. GI:
Abdominal pain, nausea, vomiting, GI bleeding. Necrotizing enterocolitis can occur
and is often fatal. Disseminated infections: Signs and symptoms of dissemination are
organ specific. Central nervous system (CNS) manifestations include altered mental
status and coma.
Diagnosis: Patient history, risk factors, clinical presentation, and signs and symptoms suggest the
diagnosis. Fluid washings from the sinuses and/or lungs can be sent for microscopy or
fungal culture. Tissue biopsies can also be obtained and examined by pathology.
Treatments: Early identification of the disease process followed by surgical debridement of infected
tissues and cavities and treatment with antifungal medications improves outcomes.
Mucormycosis is resistant to fluconazole and voriconazole. Effective medications
include amphotericin B, posaconazole, and isavuconazole.
Pearls: Risk factors for mucormycosis include uncontrolled diabetes, diabetic ketoacidosis
(DKA), compromised immune systems, hematologic malignancies, stem cell and
whole organ transplant recipients, and treatment with deferoxamine for chelation of
iron overloaded states.
166
CHAPTER 68 MUCORMYCOSIS
Mucormycosis uc
or, Rhizopu
s
(Zygomycosis)
ella
Lich
am
ei Fungi
th
mi h
a Cu n n i n g
ors
Risk Fact
•Diabetes
•DKA
ised
omprom
•Immunoc
ancy
at o lo g i c Malign
•Hem
ents
ra n sp l an t Recipi
•T
rapy
xa m in e The
•Defero
Rhinocerebral Pulmonary
Mucormycosis Mucormycosis
167
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PART 7
SEXUALLY
TRANSMITTED
DISEASES
PART 7 SEXUALLY TRANSMITTED DISEASES
Description: Gonorrhea is a common cause of urethritis in men and cervicitis in women. It is the
second-most–common reportable sexually transmitted disease in the United States.
Signs and Symptoms: Men typically develop urethritis and present with a purulent urethral discharge and
dysuria. Unilateral testicular pain and swelling are indicative of epididymitis and/or
epididymo-orchiditis.
In women, the infection often affects the cervix and can progress into the upper
genital tract causing salpingitis and pelvic inflammatory disease (PID). In cervicitis,
symptomatic women may complain of discharge, intermenstrual bleeding, dyspareunia,
urethritis, dysuria, and pelvic pain. On exam, cervical discharge and friability are likely
to be present. In PID women will have more frank abdominal pain with systemic
symptoms such as fever, chills, nausea, and vomiting. Physical exam in PID will reveal
signs of cervicitis, cervical motion tenderness, adnexal tenderness, and peritonitis.
Tubo-ovarian abscess can occur as a late complication of untreated PID. PID can
also lead to infertility or increased risk of ectopic pregnancy and can cause perihepatic
adhesions (Fitz-Hugh-Curtis syndrome).
Extragenital infection can occur in the rectum, pharynx, and conjunctiva. Lastly,
disseminated gonococcal infection (DGI) can occur and classically presents as either
(1) a triad of polyarthritis, tenosynovitis, and dermatitis, or (2) septic arthritis.
In septic arthritis, the knee is most commonly affected. Disseminated gonococcal
meningitis and endocarditis can also occur, but are rare.
Diagnostic Testing: Culture and nucleic acid amplification testing (NAAT) are available for the
diagnosis of gonorrhea. Since NAAT is not FDA approved for the diagnosis of
rectal, oropharyngeal, or conjunctival gonorrhea, culture is indicated. Gram stain
(male urethral discharge only) will reveal polymorphonuclear leukocytes with
intracellular gram-negative diplococci.
Treatments: The Centers for Disease Control and Prevention (CDC) recommends treatment
of uncomplicated gonococcal infections with ceftriaxone 250 mg IM and 1 g of
oral azithromycin. Azithromycin empirically covers for chlamydia and is thought
to reduce the likelihood of emerging gonococcal resistance to cephalosporins.
Epididymo-orchitis, prostatitis, and proctitis are treated with IM ceftriaxone and
10 days of oral doxycycline. Conjunctivitis should be treated with 1 g of ceftriaxone
IM and 1 g of oral azithromycin. Disseminated gonorrhea requires more-frequent
and higher doses of ceftriaxone. PID is treated with ceftriaxone and doxycycline
1/2 metronidazole. IV administration and hospital admission may be required.
170
CHAPTER 69 GONORRHEA
is
ea
Ne
e
Gr
am cc
i
Diplo
Meningitis
Burns Like Fire
Upon Urination Gonococcal
(Urethritis) Conjunctivitis
Endocarditis
Septic
Arthritis
Gonococcal
Pharyngitis
Disseminated
Gonorrhea
Known to most of
you as the clap!
Fitz-Hugh-Curtis
PID Syndrome
Cervicitis
Ceftriaxone 250 mg IM
171
PART 7 SEXUALLY TRANSMITTED DISEASES
Description: Human papillomavirus is a dsDNA virus and is considered the most common
sexually transmitted infection worldwide. There are more than 200 types of HPV,
each with an inherent risk of causing cancer. HPV 6 and HPV 11 are highly
associated with anogenital warts, causing about 90% of cases. HPV 16 and HPV
18 are closely linked to cervical cancer, with HPV 16 also highly associated with
oropharyngeal, anal, vulvovaginal, and penile cancers.
Signs and Symptoms: Many HPV infections are subclinical or asymptomatic. When anogenital warts
occur, they can appear externally on the foreskin, glans penis, penile shaft, scrotum,
perineum, anus, and vulva. Internal warts may appear within the pharynx,
intravaginally, on the cervix, or within the rectum. Warts tend to be painless but
can become inflamed or pruritic. Warts may be single or multiple, flat, raised,
pedunculated, and/or cauliflower-like in appearance. Color can vary from
hypopigmented, skin toned, erythematous, to hyperpigmented.
Diagnostic Testing: This is typically a visual diagnosis. Biopsy can be obtained to confirm the diagnosis
and to rule out cancer. Women should be screened with Pap testing (cytology) to
look for abnormal cells in accordance with the American College of Obstetricians
and Gynecologists (ACOG) guidelines. Abnormal Pap testing is typically followed by
colposcopy and tissue biopsy. In 2014 the FDA approved a DNA test that screens
cells obtained from the cervix for high-risk HPV strains (hrHPV). Co-testing with
Pap and hrHPV is recommended every 5 years for women age 30 and older.
172
CHAPTER 70 CONDYLOMATA ACUMINATA
Condylomata Acuminata
(Anogenital Warts)
DNA Virus
ds
HPV 16 & 18
s (HPV )
Human P
Cancer
HPV 6 & 11
Warts
ap
ru
o ll o mavi
:
a c cine
tV 8
-Valen1, 16, 1 2, 58
9 1 ,5
HPV PV 6, 33, 45
H 1,
3
HPV
173
PART 7 SEXUALLY TRANSMITTED DISEASES
Lifecycle The adult pubic louse is infectious and passed from human to human by close
contact. Adult females will lay and attach eggs (nits) to hair shafts. These eggs hatch
and release nymphs that go through three molts before becoming adults. Adults
need a blood meal to survive and can only live off of humans for 2 days.
Description: Pubic lice (Phthris pubis) are topical ectoparasites that commonly attach to pubic
hair and are sexually transmitted. They are 1–3 mm long, broad bodied, and
resemble crabs when magnified (hence the name). In addition to pubic hair, they
can also affect the eyelashes (pediculosis ciliaris), beards, mustache, and hair in the
axilla or lower abdomen. Shared bedding, towels, or clothing may also be modes
of transmission. However, despite what your friend tells you, pubic lice cannot be
transmitted via a toilet seat.
Signs and Symptoms: The saliva of the louse causes intense itching. Small spots of blood may be noticed in
an infected individual’s undergarments.
Diagnostic Testing: Diagnosis is made via the visualization of nits (eggs) or pubic lice attached to hair
shafts on a person’s body. A magnifying glass is often helpful in making the diagnosis.
Treatments: Permethrin 1% lotion can be applied to the affected area and washed off after 10 minutes.
The affected area should be retreated 10 days after the first treatment. Alternative
regimens recommended by the Centers for Disease Control and Prevention (CDC)
include malathion 0.5% lotion applied and left on for 8–12 hours prior to being
washed off or ivermectin 250 mcg/kg orally once and repeated 2 weeks later. For
pediculosis ciliaris, apply petroleum jelly to affected eyelids 4 times a day for 10 days.
Sexual partners within the previous 30 days should be offered treatment.
174
CHAPTER 71 PUBIC LICE
is
(Crabs)
P
1–3 mm
Incubation:
12 Hours–7 Days
Eyelashes
Beard or Mustache (Pediculosis Ciliaris)
Axilla
Pubic Hair
(Pediculosis Pubis)
(Phthiriasis Pubis)
Abdominal Hair
175
PART 7 SEXUALLY TRANSMITTED DISEASES
Signs and Symptoms: Primary infection is characterized by the presence of one or more firm, painless,
nonpruritic chancre(s). Without treatment, secondary syphilis will occur 4–10 weeks
later and often presents as a symmetric, nonpruritic, reddish-pink rash on the trunk,
palms, and soles. Lesions known as condyloma latum may also appear on the mucous
membranes. Without treatment, these symptoms resolve over 3–6 weeks, and the
disease enters a latent (dormant) phase. Without treatment, about one third of
patients will develop tertiary syphilis sometime over the next 3–15 years. Tertiary
disease presents as either gummatous syphilis, neurosyphilis, or cardiovascular
syphilis. Gummas are soft, noncancerous growths that often occur in the skin, liver, or
bone. Some signs of neurosyphilis include poor balance, tabes dorsalis, and Argyll
Robertson pupils. Syphilitic aortitis, resulting in an aortic aneurysm, is the most
common form of cardiac syphilis. Congenital syphilis is discussed elsewhere, but
some signs of disease include saddle nose, snuffles, saber shins, Clutton joints, and
notched Hutchinson teeth.
Diagnostic Testing: Darkfield microscopy or direct fluorescent antibody testing can be performed on
fluid or smears from lesions. Serological tests are either nontreponemal (screening)
or treponemal specific (confirmatory). RPR, VDRL, and TRUST tests are used for
screening purposes. Positive results should be followed up with confirmatory,
treponemal-specific testing, such as T. pallidum enzyme immunoassay (TP-EIA) or
fluorescent treponemal antibody absorption (FTA-ABS). Rapid finger-stick diagnostic
tests are also available. Patients who have previously had and been treated for syphilis
will continue to test positive for the disease using these various antibody tests.
Treatments: The treatment of choice is benzathine penicillin G 2.4 million units IM 3 1 for primary,
secondary, or latent infections less than 1 year’s duration. Latent infections of more
than 1 year’s duration or of an indeterminate age and tertiary infections other than
neurosyphilis should receive benzathine penicillin G 2.4 million units IM weekly 3 3.
Neurosyphilis is very difficult to treat and requires 18–24 million units continuous IV
infusion for 10–14 days. Penicillin-allergic patients should be desensitized and treated
with penicillin. Azithromycin as a 2-g single oral dose is an alternative option for early
infection; however, resistance is possible. Doxycycline and ceftriaxone can be used as
alternative treatments; however, benzathine penicillin G remains the preferred
treatment.
176
CHAPTER 72 SYPHILIS
Syphilis m a p al l
ne i
(The Great Imitator)
du
Trep
m
Sp
iro c hete
1º Painless
Chancre
PRIMARY
Chancre 2º Syphilis
Onset ≈ 21 MSM Onset
Days 4-10 Weeks
Symmetric Condyloma
2º Symptoms Latent 3º Syphilis
Rash on Latum on
Resolve in Syphylis = Onset
SECONDARY
Trunk, Mucous
3-6 Weeks Asymptomatic 3-15 Years
Palms/Soles Membranes
Gummas TERTIARY
3º Argyll-
3º Tabes Syphilitic Skin
3º Gummas Cardiovascular Robertson
Neurosyphilis Dorsalis Aortitis Liver
Syphilis Pupil
Bone 3° Gumma
CONGENITAL
1° Painless Chancre
2° Rash
Palms & Soles
177
PART 7 SEXUALLY TRANSMITTED DISEASES
Description: Chlamydia is a common cause of urethritis in men and cervicitis in women. It is the
most common reportable sexually transmitted disease in the United States and is
frequently asymptomatic in both men and women. Given its “silent” and asymptomatic
nature, all sexually active women ,25 years old and women 25 years old at higher
risk of infection should be screened for chlamydia annually.
Signs and Symptoms: Symptomatic men typically develop urethritis and present with dysuria and a clear,
scant urethral discharge. Epididymitis and/or epididymo-orchiditis can also occur,
causing unilateral testicular pain and swelling. Chlamydia may cause prostatitis in
some men.
In women, the infection often affects the cervix and can progress into the upper
genital tract, causing salpingitis and pelvic inflammatory disease (PID). In cervicitis,
symptomatic women may complain of discharge, intermenstrual bleeding, dyspareunia,
and pelvic pain. Dysuria can occur with urethritis. On examination, cervical discharge
and friability may be present. Pelvic inflammatory disease can be asymptomatic and
insidious or acute. Acutely, women with PID will have frank pelvic or abdominal pain
with systemic symptoms like fever, chills, nausea, and vomiting. Physical exam findings
consistent with PID include signs of cervicitis, cervical motion tenderness, adnexal
tenderness, and peritonitis. Tubo-ovarian abscess can occur as a late complication of
untreated PID. PID can also lead to infertility or increased risk of ectopic pregnancy
and can cause perihepatic adhesions (Fitz-Hugh-Curtis syndrome).
Chlamydia can cause proctitis as a result of recipient anal intercourse and
conjunctivitis if the eyes are exposed to infectious secretions. Chlamydial infections
can lead to reactive arthritis in some patients, mostly Caucasian males who are
HLA-B27 positive.
Diagnostic Testing: Nucleic acid amplification testing (NAAT) is now considered the gold standard
for diagnosing chlamydia, and a rapid version is available that can provide results
in 90 minutes.
Treatments: For uncomplicated chlamydial urethritis or cervicitis, the Centers for Disease
Control and Prevention (CDC) recommends treatment with a single 1-g oral dose
of azithromycin or doxycycline 100 mg orally, twice a day for 7 days. Alternate
antibiotic choices include erythromycin, levofloxacin, and ofloxacin. To cover for
gonorrhea, 250 mg of IM ceftriaxone is often given empirically. Epididymo-
orchitis, prostatitis, and proctitis should be treated with IM ceftriaxone and
10 days of oral doxycycline. PID is treated with ceftriaxone and doxycycline 1/2
metronidazole. IV administration and hospital admission may be required.
178
CHAPTER 73 CHLAMYDIA
Chlamydia a tracho
ydi
m
m
a
atis
Chl
ar
Gram
llul
ce
Ob a
ligate Intr
Asymptomatic PID
wrecking balls!!!
Cervicitis
Prostatitis
Urethritis
Orchitis
Epididymitis
Opthalmia
Neonatorum Pneumonia
Proctitis
179
PART 7 SEXUALLY TRANSMITTED DISEASES
Geographic Regions Affected: Poor and resource-limited areas of Africa, Asia, the Middle East, Australia, Pacific
Islands, Central and South America. The highest incidence is in Africa.
Signs and Symptoms: Trachoma and its manifestations are categorized as either acute (active and
inflammatory) or chronic (cicatricial and characterized by scarring). Active trachoma
is most common in young children and is often asymptomatic or manifests as
conjunctivitis with ocular discharge. Inflammation leads to the formation of
characteristic follicles on the upper tarsal conjunctiva (undersurface of the upper
eyelid). Over time, the tarsal conjunctiva forms scar tissue, distortion of the eyelid,
and trichiasis (inversion of the eyelashes). This is the cicatricial or chronic stage of
the disease. In chronic trachoma the inverted eyelashes cause continued irritation
of the eye, corneal opacification, and blindness.
Diagnostic Testing: The disease is often diagnosed clinically through screening programs in endemic
areas of the world. The World Health Organization (WHO) has developed The
Simplified WHO Trachoma Grading System to categorize the severity of disease
based on ocular findings on clinical exam.
Treatments: The WHO recommends one of two antibiotic treatments for trachoma. Oral
azithromycin given as a single 20 mg/kg dose in children or 1 g dose for adults is the
preferred treatment. It is safe, easily tolerated, clears the nasopharynx of infectious
organisms, and as a single dose has excellent compliance rates. The alternative is 1%
topical tetracycline ophthalmic ointment applied twice daily for 6 weeks. The topical
is less expensive but has a lower rate of compliance given the duration of therapy and
the discomfort associated with application. Surgery is indicted when trichiasis is
present.
Pearls: The WHO is working diligently to eliminate blindness caused by trachoma by 2020 and
has developed the SAFE initiative. This is a combination of efforts that includes Surgery,
Antibiotics, Facial cleanliness, and Environmental improvement. For more information,
please visit the International Trachoma Initiative website at www.trachoma.org.
180
CHAPTER 74 TRACHOMA
Trachomatous Inflammation
Trachomatous Scarring
Fly-to-Eye
Transmission
Dishcharge
Trichiasis
(Inverted Eyelashes)
Hand-to-Eye Coneal
Transmission Opacity
181
PART 7 SEXUALLY TRANSMITTED DISEASES
Signs and Symptoms: The classic triad of nongonococcal urethritis, conjunctivitis, and asymmetric
oligoarthritis gave rise to the mnemonic: “Can’t see, can’t pee, can’t climb a tree.”
Mucocutaneous lesions (aphthous stomatitis), enthesitis (heel pain, plantar fasciitis,
Achilles tendonitis), and cardiac manifestations may also occur. The condition may
resolve spontaneously after several weeks to months or can become chronic.
Diagnostic Testing: The workup is similar to that of rheumatoid arthritis. Labs would include a complete
blood cell count, complete metabolic panel, CRP, SED rate, HLA-B27 marker,
rheumatoid factor, and anti-cyclic citrullinated peptide (anti-CCP) test. A urine test
for chlamydia and stool sample for infectious enteropathies can also be obtained as
part of the workup. Arthrocentesis performed on a joint with effusion would be
gram stain and culture negative for bacteria.
182
CHAPTER 75 REACTIVE ARTHRITIS
183
PART 7 SEXUALLY TRANSMITTED DISEASES
Description: Herpes simplex is a life-long viral infection caused by either the HSV-1 or HSV-2
virus. Infections are classified as either primary or recurrent. Primary infections
occur when a patient is initially infected with either HSV-1 or HSV-2 for the first
time; recurrent infections or “outbreaks” occur when the HSV infection is reactivated.
Recurrent infections can occur under stress, tend to be milder than initial infections,
heal more quickly, and depending on frequency, may benefit from suppressive
therapy. Since HSV viral shedding can occur without obvious lesions, people might
not realize they are infectious.
Signs and Symptoms: Herpetic lesions appear the same in both primary and recurrent infections. They
begin as papules, then progress to vesicles, ulcerations, and then crust over and
heal without scaring. In addition to localized herpetic lesions, primary infections
often include systemic symptoms such as fever, malaise, headache, and regional
lymphadenopathy. Recurrent infections or “outbreaks” often have a prodromal
burning or tingling sensation that precedes the appearance of a herpetic lesion.
HSV-1 transmission via skin-to-skin or skin-to-mat contact in wresting is known as
herpes gladiatorum. Herpes gingivostomatitis is a herpes simplex infection of the
mouth and gums, herpes simplex of the finger is known as whitlow, and herpes
simplex keratitis is an infection of the cornea.
Diagnostic Testing: Viral culture, PCR testing, direct fluorescent antibody (DFA) testing, and/or IgM/IgG
serology can be obtained. A Tzanck smear, a microscopy slide prepared with scrapings
from an unroofed blister, can be obtained to look for multinucleated giant cells. Tzanck
smears are an outdated mode of testing but are included for historical purposes.
Treatments: Acyclovir, valacyclovir, or famciclovir can be taken orally to decrease the duration of
symptoms, hasten healing, and decrease viral shedding. The dosages and duration
of treatment required for episodic recurrences are less than those required for initial
episodes. Medications can be prescribed for chronic daily suppression for those with
frequent outbreaks. Acyclovir is available for oral, topical, and IV administration.
Foscarnet can be used in cases of acyclovir resistance. IV acyclovir is used in cases of
herpes meningitis.
184
CHAPTER 76 HERPES SIMPLEX
May I personally
recommend Herpes!
Herpetic
Labial Simplex
Keratitis
Genital
“Fever Blister”
Gingivostomatitis “Cold Sore”
Genital
Gladiatorum
Penile
Shaft
Whitlow
185
PART 7 SEXUALLY TRANSMITTED DISEASES
Signs and Symptoms: Trichomoniasis tends to cause more symptoms in women than in men: about
50% of infected women are symptomatic compared to 25% of infected men. In
addition, infected women often develop symptoms over time, whereas men can
often clear the infection spontaneously. Symptomatic women may complain of
pelvic pain, dysuria, dyspareunia, vaginal burning, itching, and a scant, frothy
green, malodourous discharge. On speculum exam, the cervix may have punctate
hemorrhages referred to as “strawberry cervix.” Men, when symptomatic, can
present with dysuria and a urethral discharge.
Diagnostic Testing: On saline wet mount, motile trichomonads may be seen swimming among a sea of
increased white blood cells. Vaginal pH tends to be .4.5. Additional tests include
nucleic acid amplification tests (NAATs), rapid antigen detection tests, and culture.
Culture has essentially been replaced by the newer molecular detection tests.
Treatments: As per recommendations from the Centers for Disease Control, metronidazole or
tinidazole as a single 2 g oral dose is the recommended regimen. The alternative
regimen calls for metronidazole 500 mg orally, twice daily, for 7 days. Current sex
partners should be referred for treatment.
186
CHAPTER 77 TRICHOMONIASIS
Trichomoniasis
o nas vag
om i
na
Tric
lis
Incubation: 4–28 Days
n
Fl a
ge
oa
llat z
e d Pr o t o
Strawberry
Cervix
187
PART 7 SEXUALLY TRANSMITTED DISEASES
Description: Scabies (Sarcoptes scabiei) is a topical ectoparasite spread by close personal contact.
The disease is characterized by intense pruritus (itching) caused by sensitization to
the mite’s feces. Initial infections have a longer incubation and delayed onset of
pruritus, whereas repeat infections (the patient is already sensitized) have a more
rapid onset of symptoms. Severe infections with extremely high mite burdens are
referred to as Norwegian or crusted scabies and are more common in the infirm,
elderly, immunocompromised, and homeless.
Signs and Symptoms: The hallmark symptom is intense pruritus, often worse at night. Patients may also
develop a small papular rash at infected areas and fine burrows may be visualized in
the interdigital web spaces. Common sites of infection include the wrists, elbows,
axilla, groin, waist, small of back, popliteal regions, and between the shoulder blades.
The face and scalp are typically spared, except in severe cases with high mite burden.
Infants and the elderly may have facial involvement.
Diagnostic Testing: Diagnosis is often made via history and characteristic skin findings. Skin scrapings
can be obtained for definitive diagnosis.
Treatments: Topical application of permethrin 5% cream applied to all areas of the body, sparing
the face, and left on for 8–14 hours followed by a shower and repeated in 1–2 weeks.
Oral ivermectin 200 mg/kg as a single dose and repeated 2 weeks later is an alternative
first-line regiment. Lindane 1% can be applied and left to sit on the body for 8 hours
before washing off as well. Lindane should never be used in infants and children, as it
can cause seizures and is considered a second- or third-line agent in adults given its
neurotoxicity. Norwegian scabies requires treatment with daily topical permethrin
and frequent doses of oral ivermectin. Antihistamines can decrease pruritus. Since
the pruritus is caused by a reaction to the feces and not the mite itself, itching can
continue for weeks after initial treatment.
Pearls: Scabies can spread rapidly in crowded conditions such as nursing homes, prisons,
homeless shelters, and refugee camps. Crusted or Norwegian scabies is highly
contagious. Scabies mites cannot survive off of the human body for more than
3 days.
188
CHAPTER 78 SCABIES
Scabies
(Seven Year Itch) p te s s c a
co
bi
S ar
ei
Incubation Period:
Initial Infection:
siz
e:
m
2–6 Weeks
0.25–0.4 m
Repeat Exposure:
Rapid Onset
Help
me!
Common Sites of
Rash Highlighted
189
PART 7 SEXUALLY TRANSMITTED DISEASES
Geographic Regions Affected: Some subtropical and tropical regions of the world including the Caribbean and
Africa. The disease is sporadic and rare in the United States.
Signs and Symptoms: Chancroid begins as a papule or nodule at the site of inoculation that evolves into
a painful, well-circumscribed, nonindurated, genital ulcer with ragged edges.
Autoinoculation can occur. About 50% of men will have a single ulcer, whereas for
women, multiple ulcers is the norm (kissing ulcers). Tender inguinal lymphadenopathy
is common and suppurative lymphadenopathy and significant tissue destruction can
occur with untreated disease progression.
Diagnostic Testing: On Gram stain, organisms often appear in long, parallel trails with a “school of fish”
appearance. If culture is pursued, chocolate agar works best. Since H. ducreyi is
extremely difficult to culture, most cases are diagnosed based on clinical findings
and ruling out other, more common, causes of genital ulcers. In chancroid, one or
more painful genital ulcers are suggestive of the disease, painful genital ulcers with
tender lymphadenopathy are highly suggestive of the disease, and painful ulcers with
suppurative lymphadenopathy is pathognomonic. A presumptive diagnosis of
chancroid can be made in patients with any of the above presentations, a negative
darkfield or serology for syphilis (Treponema pallidum), and a negative herpes simplex
(HSV) PCR or viral culture.
Treatments: As per the Centers for Disease Control and Prevention (CDC) STD Treatment
Guidelines, a variety of antibiotics are effective at treating this condition. The
recommended regimen is azithromycin 1 g orally as a single dose, ceftriaxone 250 mg
IM as a single dose, ciprofloxacin 500 mg twice daily for 3 days, or erythromycin
500 mg orally three times a day for 7 days. Azithromycin or ceftriaxone have the
convenience of single-dose therapy.
190
CHAPTER 79 CHANCROID
Chancroid mo
philus du
c
rey
(Soft Chancre)
Ha
i
Fast
lus
ou
cil
i
ba
di
s
Co cco
Incubation: 4-10 days Chocolate agar
Haemophilus ducreyi
“You Do Cry!”
(Painful)
Inguinal
Lymphadenopathy
Bubo
Soft Chancre
DIAGNOSTIC CRITERIA
1) One of more painful ulcers suggestive
2) Painful genital ulcer + tender lymphadenopathy highly suggestive
3) Painful ulcers + suppurative adenopathy pathognomonic
4) Treponema pallidum - darkfield
5) Ulcers not typical of HSV or are HSV -
191
PART 7 SEXUALLY TRANSMITTED DISEASES
Geographic Regions Affected: Some tropical regions of the world including Papua New Guinea, the Caribbean,
central Australia, India, Brazil, and southern Africa. The disease is rare in the
United States.
Description: Donovanosis is a sexually transmitted disease that causes painless, slowly progressive,
chronic, beefy-red ulcerations on the genital and perineal areas without significant
lymphadenopathy.
Signs and Symptoms: Donovanosis begins as a small, painless papule or nodule that evolves into a beefy-red,
friable ulcer. The ulcer is also painless, has a granulomatous base, expands slowly,
and can spread via autoinoculation. Satellite lesions can occur and lymphadenopathy
is notably absent or minimal. As the ulcer heals, scar tissue can develop, causing
lymphedema and disfigurement of the genital.
Diagnostic Testing: The organism is extremely difficult to culture and most cases are diagnosed based
on clinical appearance. A smear or crush preparation can be obtained from the
margin of an active ulcer and prepared for microscopy using Giemsa, Wright, or
Leishman stain. Microscopy often reveals the pathognomonic Donovan bodies:
large, intracytoplasmic, encapsulated bodies, found within macrophages swabbed
from the site of ulceration.
Treatments: As per the Centers for Disease Control and Prevention (CDC) STD Treatment Guidelines,
a variety of antibiotics are effective at treating this condition. The recommended regimen
is azithromycin 1 g orally per week or 500 mg orally per day for at least 3 weeks and until
all lesions have completely healed. Doxycycline, ciprofloxacin, erythromycin, or TMP/
SMX can all be used as alternative single-agent daily regimens for at least 3 weeks and
continued until all lesions have completely healed. Long-term antibiotic treatment may
be necessary for the ulcers to completely heal, and partial treatment can lead to disease
reoccurrence.
192
CHAPTER 80 DONOVANOSIS
Donovanosis
(Granuloma inguinale) la granulo
iel
m
s
K l eb
atis
Incubation: 1–12 Weeks Gr
am Rod
Can be mistaken
for syphilis!
Beefy Red
Ulcer
Wright,
Giemsa, or
Leishman Stain Donovan Bodies
193
PART 7 SEXUALLY TRANSMITTED DISEASES
Candida Vulvovaginitis: Candidiasis is an overgrowth of Candida albicans or C. glabrata yeast within the
lower genital tract. It is often associated with antibiotic use. Women often complain
of intense pruritus and a thick, white, curd-like, vaginal discharge. Vaginal pH is
,4.5 and KOH test is positive for pseudohyphae and candida buds. Wet mount is
negative for trichomonads and Gram stain will reveal increased white blood cells.
Treatment includes topical azole antifungals or oral fluconazole.
Bacterial Vaginosis: BV occurs when there is a shift in the normal vaginal flora from Lactobacillus
to other, mostly anaerobic, species including Gardnerella vaginalis, Ureaplasma,
Mobiluncus, Mycoplasma, and Prevotella. BV has a higher prevalence in minority
populations and females with multiple sex partners. Infected women often complain
of a fishy vaginal odor, usually more noticeable after sexual intercourse. Discharge
is typically thin, copious, grayish-white to yellow, and has a fishy odor. Vaginal pH
is increased .4.5, KOH test is negative for pseudohyphae or candida buds, but
does have a “fishy” or amine smell (1whiff test). Wet mount is negative for
trichomonads and Gram stain will reveals clue cells (vaginal epithelial cells covered
with coccobacilli bacteria). Preferred treatment is metronidazole 500 mg by mouth
twice daily for 7 days, intravaginal metronidazole gel 0.75% daily for 5 days, or
intravaginal clindamycin cream 2% daily for 7 days.
194
CHAPTER 81 VAGINITIS
Vaginitis
Bacterial
Name Vulvovaginitis Trichomoniasis
Vaginosis
195
PART 7 SEXUALLY TRANSMITTED DISEASES
Causative Agents: Molluscum contagiosum virus (MCV), genotypes 1–4, with genotype 1 responsible
for the vast majority of infections.
Description: Molluscum contagiosum is a viral infection of the skin that gives rise to small, raised,
waxy, flesh-colored lesions with a central dimple. The virus is spread via skin-to-skin
contact and lesions can arise anywhere on the skin except palms and soles. Lesions
are often found on the face, trunk, axilla, and popliteal regions. When occurring
on the genitals, the lesions may be the result of sexual transmission. The disease
is common in children, the immunocompromised, and those who participate in
contact sports.
Signs and Symptoms: Molluscum contagiosum is diagnosed by the presence of characteristic appearing
dome-shaped, umbilicated, waxy appearing papules measuring 2–5 mm in size.
The lesions may be pruritic and become inflamed over time. Lesions often resolve
spontaneously without treatment over several months and tend not to scar.
Treatments: Conservative treatment and reassurance can be provided. If patients wish to pursue
more aggressive treatments, options include cryotherapy, curettage, cantharidin, and
podophyllotoxin.
196
CHAPTER 82 MOLLUSCUM CONTAGIOSUM
Molluscum Contagiosum
Contagios
m
(MC, Water Warts)
um
u
M o l l us c
DNA
Virus
Face
MCV 1-4
Childhood
Po x v i r u s
HIV/Immunocompromised
Sexually Transmitted
Contact Sports Armpits
Arms
Trunk
2–5 mm Genitals
Umbilicated (STI)
Dome-Shaped
Waxy
Papules
197
PART 7 SEXUALLY TRANSMITTED DISEASES
Geographic Regions Affected: Subtropical and tropical regions of the world. There is an increasing incidence
among men who have sex with men (MSM) in the United States, the European
Union, and Australia.
Signs and Symptoms: Primary LGV presents as a painless papule or shallow ulcer at the site of inoculation
3–30 days after initial exposure. The ulcer can be present on the penis, vaginal wall, or
rectal mucosa and often heals over a 10-day period. Treatment is often delayed, given
the painless nature of the lesion and/or lack of awareness of its presence. Secondary
LGV can present either classically as swollen unilateral inguinal lymphadenopathy
(buboes) or as proctocolitis with pain, tenesmus, and rectal bleeding. The latter
presentation is more common in MSM and is the result of having contracted the
disease via receptive anal intercourse. Tertiary or late-stage LGV is the result of
chronic, untreated disease and presents as perirectal abscesses, fistulas, anal strictures,
and/or lymphedema of the genitals.
Diagnostic Testing: Clinical presentation and sexual and travel history should heighten suspicion for
the disease. Urine, rectal swabs, and/or lymph node aspirates can be tested for
C. trachomatis by culture, direct immunofluorescence, or nucleic acid detection
(NAAT).
Treatments: The Centers for Disease Control and Prevention (CDC) STD Treatment Guidelines
recommend doxycycline twice daily for 21 days as the preferred regimen or erythromycin
four times daily for 21 days as the alternative. Azithromycin 1 g orally once a week for
3 weeks may also have some efficacy.
198
CHAPTER 83 LYMPHOGRANULOMA VENEREUM
Lymphogranuloma Venereum
(LGV)
a tracho
ydi
m
m
a
atis
Chl
1˚ stage: Painless Ulcer
3–30 Days
2˚ stage: Lymphadenopathy
Bubos L1, L2, L3
MS
M
Painless Unilateral
Ulcer 1˚ Lymphadenopathy/
Bubos 2˚
199
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PART 8
PULMONARY
PART 8 PULMONARY
Geographic Regions Affected: All cases of MERS have been linked to exposure to the Arabian Peninsula.
Description: MERS is a severe respiratory tract infection caused by a novel coronavirus. The first
reported case occurred in Saudi Arabia in 2012 and the largest outbreak outside the
Middle East occurred in South Korea in 2015. The disease is thought to be transmitted
from camels to humans, but it can also be transmitted from person to person.
Signs and Symptoms: Infections from MERS-CoV are not fully understood and may cause a wide spectrum
of illness, with less-severe cases avoiding clinical detection. Those patients with
severe illness often present with fever, chills, malaise, myalgia, headache, shortness
of breath (SOB), and nonproductive cough. Nausea, vomiting, abdominal pain, and
diarrhea may also occur. Some patients may present atypically with gastroenteritis
preceding severe pneumonia. MERS can cause severe pneumonia, adult respiratory
distress syndrome (ARDS), renal failure, and death. The Centers for Disease Control
and Prevention (CDC) reports a high mortality rate, somewhere between 30%
and 40%.
Diagnostic Testing: The CDC recommends obtaining several specimens of bodily fluid for testing
with polymerase chain reaction (PCR) in patients under investigation (PUI) for
MERS. Specimens should be obtained via nasopharyngeal swab, sputum sample
or broncheoalveolar lavage (BAL), and serum. Those with symptoms for more than
14 days prior to presentation and/or testing can also have blood sent for serology.
More information on diagnostic testing is available on the CDC website.
Pearls: To reduce the likelihood of contracting MERS, the World Health Organization
encourages people with comorbidities and/or compromised immune systems to
avoid contact with camels while visiting the Arabian Peninsula. Good handwashing
and hygiene are encouraged for all people with contact with camels and, in general,
people are discouraged from drinking camel milk or urine.
202
CHAPTER 84 MIDDLE EASTERN RESPIRATORY SYNDROME
Novel Coronavirus
MERS
(Middle Eastern Respiratory Syndrome)
Incubation: bB
2–14 Days n Tom at - Re
ia s
pt
er
Egy
voi
r
Fever, Chills
Headache
PCR al
r y nge
ha
sop m
Na Sputu
BAL
um
Ser
SOB
Nonproductive
Cough
High
Mortality Abdominal
Pain
Myalgia
Nausea
Vomiting
Diarrhea
Do Not Drink
203
PART 8 PULMONARY
Reservoir: Humans
Incubation: 2–12 weeks from exposure to positive purified protein derivative (PPD) test
Description: Tuberculosis (TB) is primarily a bacterial disease of the lung caused by the aerobic,
nonmotile, acid-fast, bacillus M. tuberculosis. TB is spread via airborne droplets and
is notoriously difficult to treat, given the bacteria’s slow reproductive rate. Initial or
primary TB infections either are suppressed by the immune system or cause active
disease. A primary infection that results in active disease is referred to as primary
progressive TB. Suppression of TB occurs in 90% of primary infections and results in
latent TB. Latent TB can remain dormant for many years and, if not treated, will
become active (reactivation TB or progressive secondary TB) in about 10% of those
infected. Latent TB is not contagious, whereas active TB is. Risk factors for TB
include homelessness, incarceration, and HIV.
Signs and Symptoms: Active pulmonary TB causes fever, malaise, fatigue, night sweats, weight loss, cough,
dyspnea, pleuritic chest pain, and hemoptysis. Symptom onset is often more gradual
in cases of reactivation TB. Disease that spreads outside the lungs is referred to
extrapulmonary TB and is more common in children and the immunocompromised.
Common sites of extrapulmonary TB include the pleura, meninges, lymphatic
system, genitourinary (GU) system, and the bones.
Diagnostic Testing: PPD screening tests determine if the patient had ever had a previous exposure to
TB. Chest x-rays may show signs of active disease and may reveal miliary lesions,
consolidation, cavitary lesions, pleural effusions, nodular infiltrates, granulomas,
and mediastinal lymphadenopathy. TB has a preference for the lung apices,
predominantly on the right side. When testing for active disease, sputum samples
should be obtained for acid-fast bacilli (AFB) staining using the Ziehl-Neelsen (ZN)
stain, plated for culture and sensitivity, and tested using polymerase chain reaction
(PCR). Culture is the gold standard for diagnosis, but it takes up to 4–8 weeks for
results. Rapid diagnostic tests are available for use in developing nations.
Treatments: Latent TB is often treated with daily isoniazid with or without supplemental pyridoxine
for 9 months. Alternative regimens exist, including daily rifampin for 4 months.
Treatment of active and/or extrapulmonary TB requires multiple drugs including,
but not limited to, isoniazid, rifampin, ethambutol, streptomycin, and pyrazinamide.
Each drug has specific and common side effects, included on our illustration.
204
CHAPTER 85 TUBERCULOSIS
Tuberculosis m
teriu tuber
ac
ob
cu
lo
Myc
Miliary
sis
Nodules Langerhans Giant Cells
Consolidation
Ae
s
illu
Cavitary Mediastinal bi Acid Fast
ac
ro
cN
Lesion Nodes onmotile B
Nodule Pleural
Effusion
Night
Sweats Meningeal TB
Scrofula
Hemoptysis
Pleural
TB Airborne Droplets
Pott’s
Disease
PPD
≥5 mm HIV
TB Contact
205
PART 8 PULMONARY
Reservoir: Legionella can reside and replicate in amoebas found in aquatic environments.
Signs and Symptoms: Fever, severe headache, malaise, and myalgia are often the first presenting symptoms.
Nausea, vomiting, and diarrhea can also occur. Cough is often productive, with
occasional blood-tinged sputum and/or hemoptysis. There may be a relative
bradycardia and chest x-ray will reveal consolidated pneumonia. Confusion and
seizures may also occur.
Diagnostic Testing: Labs will reveal hyponatremia, hypophosphatemia, elevated liver enzymes,
leukopenia/leukocytosis, thrombocytopenia, increased lactic dehydrogenase
(LDH), disseminated intravascular coagulation (DIC), and possible acute kidney
injury. Confirmatory diagnosis is established by urinary antigen, cultures of
endotracheal aspirates or sputum, immunofluorescence microscopy, detection
of serum antibodies, and/or molecular amplification by polymerase chain
reaction (PCR).
Pearls: Hyponatremia and relative bradycardia are hallmarks of Legionnaires’ disease, but
not confirmatory. Pontiac fever is a brief, febrile, upper respiratory illness caused by
the inhalation of Legionella spp. aerosolized from contaminated water or potting
soil. It has a short incubation period of several hours to 3 days and is more common
in people in their 30s. Pontiac fever is self-limiting, and treatment is supportive.
206
CHAPTER 86 LEGIONNAIRES’ DISEASE
ph
i
Leg
ila
lus
Gram
acil
Incubation: 2–10 Days Fl
ob
ag c
e l l a te d Coc
Outbreaks: Summer/Fall
Confusion
Fever
Chills
Headache
Productive Cough
Blood-tinged Sputum
Hemoptysis
Relative
Bradycardia
Air Conditioner
Nausea
Vomiting
Diarrhea
Myalgia
Contaminated Water
207
PART 8 PULMONARY
Reservoir: Birds
Signs and Symptoms: The disease can vary in presentation from asymptomatic or mild to severe
respiratory illness and pneumonia. Patients most commonly present with symptoms
of atypical pneumonia including acute fever, severe headache with photophobia, and
nonproductive cough. Cough characteristically presents later in the course of illness.
Given the variations in disease presentation, symptoms are occasionally nonspecific
and, in addition to the above, can also include chills, malaise, myalgia, arthralgia,
epistaxis, abdominal pain, nausea, vomiting, and diarrhea. Hepatosplenomegaly,
hepatitis, and disseminated intravascular coagulation (DIC) may also occur.
Diagnostic Testing: Diagnosis should be considered in those patients with classic symptoms and a history
of exposure to birds. Chest x-ray can reveal any number of abnormalities, with lower
lobe consolidation the most common finding. Labs will reveal normal to mildly
increased WBC with a shift to the left. Liver enzymes are often elevated. Diagnosis is
often based on history of bird exposure and a rise of serum antibody titers. When
psittacosis is suspected, cultures are discouraged, as the bacteria is highly infectious
and can put lab workers at risk.
Treatments: Doxycycline or tetracycline are effective treatments and once initiated, patients tend
to improve within 24 hours. Azithromycin or erythromycin are considered second-line
agents and can be considered when tetracycline antibiotics are not tolerable.
208
CHAPTER 87 PSITTACOSIS
Psittacosis am
yd i a p s i t t
ac
l
Ch
(Parrot Fever)
i
I nt
ia
ac
er
c t
r
ellu
lar Ba
Incubation: 5–19 Days
Headache
Nonproductive
Cough
Epistaxis
Chills
Fever
Pneumonia
Hepatosplenomegaly
are
r f
a
-W
o
Bi
Arthralgia
Diarrhea
209
PART 8 PULMONARY
Causative Agents: Avian Influenza A Viruses: Asian H5N1 and Asian H7N9
Reservoir: Wild aquatic birds and waterfowl such as gulls, tern, ducks, geese, and swans are
the natural reservoirs. The virus can infect domesticated birds and poultry causing
disease, which can then potentially spill over to the human population.
Description: Avian influenza is a viral infection in birds caused by certain strains of the Influenza
A virus. While these specific strains are typically limited to bird-to-bird transmission,
bird-to-human transmission can occur and result in disease. Human-to-human
transmission has been reported but is extremely rare and, fortunately, not sustained.
If sustained human-to-human transmission were to occur, it could cause a global
pandemic.
Avian Influenza A viruses are classified as low pathogenic avian influenza (LPAI) or
high pathogenic avian influenza (HPAI). Birds infected with LPAI viruses can be
asymptomatic or have mild symptoms including changes to egg production. In
contrast, those birds infected with HPAI strains often have a more severe illness,
which can include respiratory symptoms and death. If introduced into a domestic
flock, avian influenza can spread rapidly and requires the eradication of infected
flocks and the quarantine of those flocks in close proximity to the outbreak.
Signs and Symptoms: In humans, Avian Influenza A (H5N1) and A (H7N9) are known to cause severe
disease. Infected patients will develop fever, chills, malaise, myalgia, headache, and
cough. Nausea, vomiting, abdominal pain, and diarrhea may occur in some patients.
These viruses have a high likelihood of causing severe pneumonia, shock, adult
respiratory distress syndrome (ARDS), multisystem organ failure, and death.
Mortality is as high as 60%.
Diagnostic Testing: Nasopharyngeal swabs can be tested for novel influenza viruses using polymerase
chain reaction (PCR). More information is available on the Centers for Disease
Control and Prevention (CDC) website.
Treatments: The CDC recommends the use or oral oseltamivir in all human cases of suspected
infection with novel influenza viruses, including avian influenza, even if more than
48 hours has passed since symptom onset. A 10-day duration of treatment may be
advisable in immunocompromised patients and those with severe illness. Outpatient
prophylaxis for 5 days with oral oseltamivir is recommended for those who have had
contact with infected patients.
210
CHAPTER 88 AVIAN INFLUENZA
Avian Influenza
Cough
No Sustained
Human-to-Human
Transmission
Coughing
Sneezing
Infected birds
must be eradicated!
Nasal Discharge
Purple Discoloration of the
Head, Comb, Wattles
Eyelids, Hock
Abnormal
Egg
Soft Egg Shape
Diarrhea
211
PART 8 PULMONARY
Reservoir: Humans
Description: Influenza is an acute febrile viral respiratory tract infection most common in
temperate climates during the winter. The disease is spread via respiratory droplets,
causes periodic epidemics, and has the potential to cause global pandemics.
Pandemics occur when a new strain of influenza emerges for which humans have
had little to no previous exposure. There are three types of influenza virus (A–C)
based on the core protein, with only types A and B causing significant disease in
humans. Type A viruses are further classified based on two specific antigens,
hemagglutinin (HA or H) and neuraminidase (NA or N), found on the surface of
the virus. These antigens are responsible for the HN classifications often seen on
annual vaccines. Since influenza viruses are constantly undergoing genetic changes via
antigenic drift (frequent and minor) and antigenic shift (infrequent and significant),
new and updated vaccinations are required each year.
Signs and Symptoms: Infected patients will develop acute fever, chills, rigors, malaise, myalgia, headache,
rhinorrhea, and nonproductive cough. Nausea, vomiting, and diarrhea may occur in
some patients, more so in children. The immunocompromised, extremes of age,
pregnant women, residents of long-term care facilities, and those with preexisting
medical conditions are more likely to have severe disease and complications.
Pneumonia, either from the influenza virus directly or secondarily from bacteria,
is one potential complication.
Diagnostic Testing: Rapid influenza diagnostic tests (RIDT) are immunoassays that detect Influenza A
and B viral antigens. Nasopharyngeal swabs can be tested for influenza viruses
using polymerase chain reaction (PCR).
Treatments: There are two classes of drugs used to treat influenza. The adamantanes include
amantadine and rimantadine, which target and inhibit function of the M2 protein
and are only effective against Influenza A. Given the increased resistance to these
drugs over the years and efficacy against both Influenza A and B, neuraminidase
inhibitors are preferred for the treatment and prophylaxis of influenza. Neuraminidase
inhibitors include oseltamivir, zanamivir, and peramivir. Oseltamivir is taken orally
and zanamivir is an inhaled powder. A newer drug, peramivir, is indicated for
treatment only (no indication for prophylaxis) and is given as a single intravenous
(IV) dose. These medications are thought to decrease the duration and severity of
illness and are only effective when initiated within 48 hours of symptom onset.
212
CHAPTER 89 INFLUENZA
Influenza ue
n za A & B V
iru
Infl
“ The Flu”
s
Incubation:1–4 Days
Average: 2 Days
Peak: Winter Headache
Malaise
Rhinorrhea
Cough
Fever
Chills
Rigors
HA: Hemagglutinin
NA: Neuraminidase
M2: M2 Protein
Neuraminidase
Inhibitors
Target
Diarrhea
NA HA NA
HA HA in Children
HA
M2
HA HA
HA M2
M2
HA Amantadine/
HA HA Rimantadine
HA NA Target
213
PART 8 PULMONARY
Geographic Regions Affected: The first cases of SARS have been traced back to the Guangdong Providence of
China and Hong Kong in 2002. From there, SARS quickly spread to other countries
around the region and world before being contained.
Description: SARS is a severe respiratory tract infection caused by a novel coronavirus. The
disease was initially thought to have been transmitted from palm civets to humans.
However, since person-to-person transmission is highly effective, the disease can
quickly spread.
Signs and Symptoms: Most patients have a several-day prodrome of fever, chills, malaise, headache,
and myalgia before developing a nonproductive cough. The cough typically gets
worse and can ultimately progress to pneumonia, adult respiratory distress
syndrome (ARDS), multisystem organ failure, and/or death.
Diagnostic Testing: Labs often reveal decreased lymphocytes and platelets with increased AST and lactic
dehydrogenase (LDH). Chest x-ray, depending on severity of illness, can reveal
bilateral infiltrates to signs of severe ARDS. Respiratory secretions, blood/serum/
plasma, and stool samples should be collected for polymerase chain reaction (PCR)
testing in accordance with Centers for Disease Control and Prevention (CDC)
guidelines. Serology is only helpful in the convalescent phase of the disease. More
information on diagnostic testing is available on the CDC website.
Pearls: In the Western hemisphere, Toronto, Canada, was hit particularly hard by SARS.
Kopi luwak, a coffee from Indonesia, is famous as the most expensive in the world
and is made from the feces of palm civets fed coffee cherries. Since many of these
animals are kept confined to small cages and force fed, the authors encourage you to
boycott this product.
214
CHAPTER 90 SEVERE ACUTE RESPIRATORY SYNDROME
SARS Coronavi
RS r
SA
us
Incubation: 2–7 Days
Prodrome
Fever
Chills
Reservoirs
Cough
Dyspnea
CXR
Bilateral Infiltrates
ARDS
Horseshoe Bat
Don’t
eat me!
L A BS
Lympho
cytes
Myalgia LDH
ALT
Platel
ets
RT-P
CR
Palm Civet
215
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PART 9
MOSQUITO-BORNE
ILLNESSES
PART 9 MOSQUITO-BORNE ILLNESSES
Geographic Regions Affected: Tropical and subtropical regions are at risk, as well as any regions that may support
the Aedes spp. mosquito. Most U.S. cases are in returning travelers; however, the
Centers for Disease Control and Prevention (CDC) has confirmed several cases of
local mosquito-borne Zika in Florida and Texas.
Description: Zika is an acute febrile mosquito-borne illness similar to but milder than dengue.
Infection is characterized by fever, arthralgia, myalgia, headache, conjunctivitis, and a
pruritic maculopapular rash that begins on the face and spreads to the rest of the body.
Most patients (,80%) are asymptomatic or have mild disease. When symptomatic,
symptoms last for about 3–7 days. Zika infections during pregnancy have been
implicated in microcephaly and other fetal brain defects, with Brazil being hit the
hardest. Guillian-Barré syndrome has also been reported following some Zika
infections.
Signs and Symptoms: Often asymptomatic, but classic signs of infection include fever, arthralgia,
conjunctivitis, and rash. The fever in Zika is low grade, unlike the high fevers of
dengue and chikungunya.
Diagnostic Testing: Symptomatic, non-pregnant individuals should receive testing of both urine and serum
by Zika virus RNA NAT (nucleic acid testing) and IgM serology tests. NAT and serology
tests for dengue and chikungunya should also be considered for individuals at risk of
exposure and presenting with compatible illness. Patients presenting within 14 days of
symptom onset can undergo NAT testing on both serum and urine. A positive result
on either or both confirms the diagnosis. Negative NAT testing should be followed by
serology. For patients presenting ≥14 days after symptom onset, NAT testing is not
indicated, and only serology should be obtained. Negative IgM serology rules out acute
infection, and positive IgM serology should be followed by plaque neutralization
reduction testing (PNRT) for disease confirmation. More detailed information and
testing algorithms for pregnant females is available on the CDC website.
Treatments: Supportive. NSAIDs should be avoided until dengue has been ruled out.
Prevention: Avoid mosquitos. Zika can be transmitted sexually, via blood transfusion, and passed
vertically from mother to child during pregnancy. The CDC has recommended that
men and women who traveled to areas where Zika is common should avoid sex or
use condoms for at least 8 weeks after return from travel and for 8 weeks (women)
and up to 6 months (men) if they had Zika or similar symptoms.
Pearls: Zika can be detected in semen for as long as 3–6 months after initial infection.
218
CHAPTER 91 ZIKA FEVER
Virus ZIK
Zika Fever Zi
ka V
Conjunctivitis
Headache
Fever
A+
Myalgia
Arthralgia
e
ytim
Da ding!
fee
Rash
Aedes aegypti
Aedes albopictus
Sexually Transmitted
219
PART 9 MOSQUITO-BORNE ILLNESSES
Vector: Aedes spp.—A. aegypti is the principal vector, but A. albopictus and A. polynesiensis
can also transmit the virus. These are all daytime-feeding mosquitos.
Reservoir: Human and nonhuman primates. Monkeys in West Africa and Southeast Asia.
Geographic Regions Affected: Tropical and subtropical regions are at risk, as well as any regions that may support
the Aedes spp. mosquito.
Signs and Symptoms: Dengue fever (DF) is an acute febrile illness characterized by retroorbital headache,
malaise, severe myalgia, arthralgia, and rash. The disease is most often asymptomatic
or mild but can be severe and progress to hemorrhage (dengue hemorrhagic fever
[DHF]) or shock (dengue shock syndrome [DSS]). While initial infections are often
mild or asymptomatic, subsequent infections tend to be worse. DHF, a more-severe
disease presentation, progresses through three phases: Febrile Phase: Symptoms
include fever, headache, myalgia, arthralgia, rash, petechiae, easy bruisability,
epistaxis, mucosal bleeding, and a positive tourniquet test. Children often present
with nausea and vomiting. Symptoms are similar to DF. Critical Phase: Characterized
by gastrointestinal (GI) hemorrhage and plasma leakage into the chest and peritoneal
cavities, occurring after the fever breaks. Abdominal pain, ascites, and dyspnea can
occur. DSS can occur in this phase unless aggressive fluid resuscitation is initiated.
Recovery Phase: Patients will begin to feel better as capillary leakage stops and fluids
begin to be reabsorbed. Bradycardia and a rash described as “white islands in a sea
of red” may be observed.
Diagnostic Testing: Labs will reveal leukopenia and thrombocytopenia. Hepatitis is common. Increased
hematocrit and decreased albumin indicate capillary leakage and impending shock.
IgM and IgG serology and polymerase chain (PCR) testing is available.
220
CHAPTER 92 DENGUE
Dengue Fever
e Fever
gu 1–DE Vi
(Breakbone Fever) NV
N
DE en
ru 4
s
D
V
Incubation: 3–14 Days
Average 4–7 Days NA s
Flaviviru
R
Triphasic Disease:
Febrile Critical
Recovery
Aedes polynesiensis
Aedes albopictus
Aedes aegypti #1
40º C
Fever
Retro-Orbital
Headache
Mucosal
Bleeding
Rash
Nausea
Vomiting
Abdominal
Pain
White Islands
in a Sea of Red
(Recovery)
221
PART 9 MOSQUITO-BORNE ILLNESSES
Geographic Regions Affected: Sub-Saharan Africa, Central and South America. Approximately 90% of all cases occur
in Africa.
Description: Yellow fever is an acute febrile mosquito-born viral illness. It is named after the
jaundice that occurs during the toxic phase of the illness.
Signs and Symptoms: Many cases are asymptomatic. Mild illness may be limited to fever and headache,
whereas moderate disease is characterized by fever, chills, malaise, headache,
myalgia, backache, nausea, and vomiting. Symptoms typically last for 3–4 days before
resolving. In approximately 15% of symptomatic cases, patients will progress to a
more toxic phase of the disease characterized by recurrence of fever, chills, jaundice,
liver failure, mucosal bleeding, hematemesis, melena, delirium, renal failure, and
shock. Mortality from the toxic phase is high, ranging between 20% and 50%.
Surviving the illness confers lifetime immunity.
Diagnostic Testing: Presumptive diagnosis is made based on travel history and signs and symptoms.
Labs will reveal elevated AST/ALT, prolonged PT and PTT, thrombocytopenia, and
an increased direct bilirubin with a relatively normal alkaline phosphatase. Yellow
fever–specific IgM and IgG levels can help confirm the diagnosis, but it is important
to note there may be some cross-reactivity with other flaviviruses. Since viremia only
lasts for about 3 days, polymerase chain reaction (PCR) testing is of limited value
unless obtained early in the course of illness.
Prevention: Avoid mosquitos. A single subcutaneous (SQ) dose of live-attenuated yellow fever
vaccine is indicated for those traveling to or living in at-risk areas or when proof of
vaccination is required to enter a specific country.
222
CHAPTER 93 YELLOW FEVER
Ye
us
ssRNA
Myalgia
RIP Bleeding
Shock
20%–5
0%
223
PART 9 MOSQUITO-BORNE ILLNESSES
Lifecycle: Malaria is contracted by the bite of an infected female Anopheles mosquito during
feeding. Liver Stage: Sporozoites are injected and migrate through the circulatory
system and infect hepatocytes in the liver. Here multinucleated schizonts form.
P. vivax and P. ovale form hypnozoites which can remain dormant or form schizonts.
Hepatic schizonts ultimately rupture, releasing merozoites capable of infecting red
blood cells. Blood Stage: Merozoites infect blood cells and develop into trophozoites
and blood cell schizonts or gametocytes. Infected blood cells will rupture, releasing
merozoites capable of infecting other red cells or male and female gametocytes
capable of being ingested by mosquitos. Sexual reproduction occurs in the mosquito’s
midgut, and mature sporozoites migrate to the mosquito’s salivary gland, ready to
infect another human at the next feeding.
Incubation: 7–30 days. Incubation periods are shorter for P. falciparum and longer for P. malariae.
Partial immunity or ineffective malaria prophylaxis may delay symptoms for weeks
or months. Also, both P. vivax and P. ovale can create dormant liver-stage parasites,
delaying disease presentation or relapse months or years after treatment.
Geographic Regions Affected: Tropical and subtropical regions. The highest rates of transmission are found in
sub-Saharan Africa and New Guinea. Malaria transmission does not occur at
high altitude, during cold seasons, in deserts, or in areas with effective mosquito
eradication programs.
Signs and Symptoms: In uncomplicated malaria, patients can present with paroxysmal fever, chills, malaise,
arthralgia, myalgia, headache, diaphoresis, tachycardia, tachypnea, abdominal pain,
splenomegaly, nausea, and vomiting. In severe malaria, patients can develop altered
mental status (AMS), seizures, shock, adult respiratory distress syndrome (ARDS),
metabolic acidosis, hemoglobinuria, renal failure, hypoglycemia, hepatic failure,
coagulopathy, and severe anemia.
Diagnostic Testing: Malaria should be suspected in patients with febrile illness and recent travel to a
region where malaria is endemic. Labs may reveal anemia, thrombocytopenia,
elevated AST/ALT, elevated bilirubin, and elevated BUN/creatinine. Thick and thin
blood smears should be obtained to detect parasites (thick) and identify the species
(thin). Blood smears can be obtained every 8 hours for several days if malaria is
suspected.
224
CHAPTER 94 MALARIA
Treatments: Treatment is tailored to the Plasmodium spp., severity of illness, pregnancy status,
and drug susceptibility based on geographic region of infection. Current Centers
for Disease Control and Prevention (CDC) guidelines should be consulted prior
to selecting a treatment regimen. Uncomplicated malaria can be treated with:
atovaquone/proguanil, artemether/lumefantrine, quinine sulfate plus doxycycline,
or mefloquine (mefloquine can cause neuropsychiatric reactions). If chloroquine
resistance is not an issue, uncomplicated malaria can be treated with chloroquine
phosphate or hydroxychloroquine. P. vivax and P. ovale require a longer duration
of treatment with primaquine to eradicate liver hypnozoites. Primaquine can cause
hemolytic anemia in G6PD-deficient patients and cannot be used during pregnancy.
Severe malaria should be treated with IV quinidine gluconate plus doxycycline or
clindamycin.
Prevention: Avoid mosquitos. Malarial prophylaxis is indicated for travelers to endemic regions
and recommendations often vary between the WHO and the CDC. The species of
Plasmodium and presence/absence of chloroquine resistance are factors to consider
when considering prophylaxis. Medications are typically started 1 day to 2 weeks
before travel and continued up to 4 weeks after return. The CDC website can be
referenced for country-specific recommendations.
225
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CHAPTER 94 MALARIA
Malaria as
m o di u m s p
Pl
p.
P. vivax*
P. falciparum*
P. malariae
Incubation: 7–30 Days P. ovale
Pro t o a
az
Shorter: P. falciparum
*Main Causative Agents
Longer: P. malariae
Typical Medical
Student Answer!
Injects
Sporozoites
Liver Cells Severe Malaria
Anopheles spp. Infected AMS/Seizures
ARDS/Shock
Metabolic Acidosis
Hypnozoites Hepatic Hypoglycemia
P. vivax Schizonts Renal Failure
P. ovale Hepatic Failure
Hemolysis Anemia/Coagulopathy
Blood Cell
Merozoites Schizont
Late
Trophozoite
Malaria Symptoms Early
Paroxysmal Fevers/Chills Trophozoite
Tachycardia/Tachypnea Gametocytes
Fatigue/Malaise
Headache/Cough
Nausea/Vomiting/Abdominal Pain Anopheles spp.
Arthralgia/Myalgia
Splenomegaly
227
PART 9 MOSQUITO-BORNE ILLNESSES
Saint Louis Encephalitis • Causative Agent: Saint Louis encephalitis virus (SLEV)—Flaviviradae
• Vector: Culex spp. – C. pipiens and C. quinquefasciatus
• Region: North and South America—Eastern and Central U.S. states
• Incubation: 5–15 days
• Symptoms: Almost all cases are asymptomatic. Those who become ill develop
fever, headache, dizziness, malaise, nausea, and vomiting. Progression to
encephalitis is much more common in older adults than children. Mortality in
neuroinvasive disease ranges between 5% and 15% and increases with age.
• Treatment: Supportive.
228
CHAPTER 95 MOSQUITO-BORNE ENCEPHALITIS
Murray Valley Encephalitis • Causative Agent: Murray Valley encephalitis virus (MVEV)—Flaviviradae
• Vector: Culex annulirostris—Common banded mosquito
• Region: Australia and New Guinea—Most common after heavy rainfalls
• Incubation: 5–28 days, Average: 7–12 days
• Symptoms: Almost all infections (99.9%) are asymptomatic. Those who become
ill develop fever, headache, fatigue, nausea, and vomiting. Encephalitis is
uncommon (0.1% overall). Mortality for neuroinvasive cases ranges between
15% and 30% with 30% to 50% of survivors exhibiting neurologic sequela.
• Treatment: Supportive.
Aedes spp.
La Crosse Encephalitis • Causative Agent: La Crosse virus (LACV)—Bunyaviridae
• Vector: Aedes triseriatus—Eastern treehole mosquito
• Region: Upper Midwestern, mid-Atlantic, and Southern U.S.
• Incubation: 5–15 days
• Symptoms: Most infections are asymptomatic. Those who become ill develop fever,
headache, fatigue, nausea, and vomiting. Encephalitis is rare and most commonly
occurs in children ,16 years old. AMS, seizures, and coma can occur with
neuroinvasive disease. Mortality in neuroinvasive disease is ,1% with neurologic
sequela reported in about 10% of survivors.
• Treatment: Supportive.
Culiseta spp.
Eastern Equine Encephalitis • Causative Agent: Eastern equine encephalitis virus (EEEV)—Togaviridae
• Vector: Culiseta melanura—Black-tailed mosquito
• Region: North, Central, South America and Caribbean—Most U.S. cases occur in
Atlantic and Gulf Coast states.
• Incubation: 4–10 days
• Symptoms: Fever, headache, nausea, and vomiting. Encephalitis occurs in 2% to
6% of infections and progresses from altered mental status (AMS) to seizures
and coma. Mortality in neuroinvasive cases is about 30%, making EEE the most
severe mosquito-borne illness in the United States. Most survivors will have
neurologic sequelae.
• Treatment: Supportive.
229
PART 9 MOSQUITO-BORNE ILLNESSES
230
CHAPTER 95 MOSQUITO-BORNE ENCEPHALITIS
Mosquito-Borne Encephalitis
oviruses
A rb
Culex spp.
Neurologic Deficits
Altered Mental Status
Flaviviridae Headache
Togaviridae Seizure
Malaise
Stiff Neck
Flaviviridae
Flaviviridae Fever
Lumbar
Puncture
Flaviviridae
Nausea
Vomiting
Togaviridae
Aedes triseriatus Culiseta melanura
Bunyaviridae Togaviridae
231
PART 9 MOSQUITO-BORNE ILLNESSES
Reservoir: Human and nonhuman primates. The World Health Organization (WHO) reports
that some nonprimates, birds, rodents, and small mammals may serve as reservoirs.
Geographic Regions Affected: Tropical and subtropical regions are high-risk areas, as well as any region that may
support the Aedes spp. mosquito. In late 2013, local transmission of chikungunya was
identified in several Caribbean countries and territories. The disease has since spread
to South America.
Signs and Symptoms: The majority (80%) of those infected will be symptomatic. Chikungunya should be
suspected patients with recent travel to endemic regions and presenting with high
fever and polyarthralgia.
Fever can be biphasic. Arthralgia is typically bilateral and symmetric, predominantly
affecting the peripheral joints of the hands, feet, wrists, and ankles. Knees, elbows,
and shoulders can also be involved, while hips are often spared. Myalgia, headache,
malaise, conjunctivitis, and nausea can also occur. A transient (3–4 day) maculopapular
rash affecting the face, trunk, and extremities is present in 40%–50% of cases. Unlike
with dengue, hemorrhage is very rare. Guillian-Barré syndrome may occur as a
post-infectious complication. Patients may develop chronic polyarthritis, with as
many as 20% still complaining of arthralgia 1 year after the initial infection.
Diagnostic Testing: Serum can be tested for the virus, viral nucleic acid, or chikungunya-specific IgM.
According to the Centers for Disease Control and Prevention (CDC), the virus can
be detected for 3 days, and viral RNA for 8 days, and IgM should be elevated within
1 week of symptom onset. IgG elevates within 2 weeks of infection. Since the
diseases have similar presentations, testing for Zika and dengue should also be
considered. More detailed information is available on the CDC website.
Treatments: Supportive
Pearls: Post-chikungunya polyarthritis can mimic rheumatoid arthritis (RA). Careful history
and diagnostic testing can help distinguish the two. Chikungunya IgG should remain
elevated for years after initial infection.
232
CHAPTER 96 CHIKUNGUNYA
Chikungunya
CHIKV
Conjunctivitis
Wrist
No Hemorrhage
Hand
Nausea, vomiting,
and diarrhea
can occur.
Knee
233
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PART 10
RAT-, FLEA-,
LOUSE-, AND
CHIGGER-BORNE
ILLNESSES
PART 10 RAT-, FLEA-, LOUSE-, AND CHIGGER-BORNE ILLNESSES
Causative Agents: Hantaviruses of the Bunyaviridae family: Hantaan River virus (HTNV), Saaremaa
virus (SAAV), Seoul virus (SEOV), Puumala virus (PUUV), and Dobrava virus
(DOBV)
Transmission: Aerosolized virus from infected rodent excreta, saliva, and urine.
Reservoir: Striped field mouse for Saaremaa (SAAV) and Hantaan viruses (HTNV); Norway rat
for Seoul virus (SEOV); bank vole for Puumala virus (PUUV); yellow-necked field
mouse for Dobrava virus (DOBV)
Geographic Regions Affected: Saaremaa virus in Central Europe and Scandinavia; Hantaan virus in East Asia;
Seoul virus worldwide; Puumala virus in Scandinavia, Western Europe, and Western
Russia; and Dobrava virus in the Balkans.
Peak Incidence: Spring and fall peaks for Saaremaa and Hantaan viruses due to mouse breeding
seasons and human agricultural practices.
Description: Hemorrhagic fever with renal syndrome (HFRS) is a viral zoonotic infection caused
by exposure to aerosolized excreta, urine, or saliva from infected rodents. The
infection has been divided into five clinical phases: febrile, hypotensive, oliguric,
diuretic, and convalescent.
Signs and Symptoms: Febrile: Flu-like symptoms predominate, including fever, chills, headache, malaise,
nausea, vomiting, diarrhea, cough, and abdominal and back pain. Conjunctivitis,
blurred vision, and a petechial rash are often present. Hypotensive: Severe capillary
leak syndrome, edema, hypotension, tachycardia, and thrombocytopenia. Oliguric:
Characterized by renal failure with proteinuria. Diuretic: Diuresis and polyuria, up
to several liters per day. Convalescent: The recovery phase, which can be lengthy.
Diagnostic Testing: Recognition of exposure to infected rodents is key. Labs will reveal thrombocytopenia,
leukocytosis with a shift to the left including immature myeloid cells and atypical
lymphocytes. Serology, polymerase chain reaction (PCR), and immunohistochemical
testing can be performed to confirm the diagnosis.
Treatments: Treatment is supportive. Ribavirin may have some benefit if given early. Hemodialysis
may be necessary. Complete recovery may take weeks or months.
236
CHAPTER 97 HEMORRHAGIC FEVER WITH RENAL SYNDROME
BV
HTNV
ssRNA
Average: 1–2 Weeks
DO
AA
V
V SE U
OV PU
Renal Failure
Shock
237
PART 10 RAT-, FLEA-, LOUSE-, AND CHIGGER-BORNE ILLNESSES
Causative Agents: American Hantaviruses of the Bunyaviridae family: Sin Nombre virus (SNV);
New York virus (NYV); Bayou virus (BAYV); Black Creek Canal virus (BCCV);
Andes virus (ANDV).
Transmission: Aerosolized virus from infected rodent excreta, saliva, and urine
Reservoir: Deer mouse (Peromyscus maniculatus) for Sin Nombre virus (SNV); white-footed
mouse (Peromyscus leucopus) for New York virus (NYV); cotton rat (Sigmodon
hispidus) for Black Creek Canal virus (BCCV); rice rat (Oryzomys palustris) for
Bayou virus (BAYV); long-tailed rice rat (Oligoryzomys longicaudatus) for Andes
virus (ANDV)
Geographic Regions Affected: United States and Canada (Sin Nombre virus); Northeastern United States (New York
Hantavirus); Southeastern United States (Bayou Hantavirus); Florida (Black Creek
Canal Hantavirus); South America (Andes Hantavirus).
Peak Incidence: Can occur throughout the year, but peaks in summer and fall.
Signs and Symptoms: Prodromal: Flu-like symptoms including fever, headache, myalgia, nausea, vomiting,
and diarrhea. Respiratory symptoms are minimal and the prodromal symptoms may be
mistaken as gastroenteritis. The duration of symptoms lasts 3–5 days. Cardiopulmonary:
Severe dyspnea, nonproductive cough, pulmonary edema, and circulatory collapse
occur. Mechanical ventilation is often required. This phase lasts only 24–48 hours.
Convalescent: The recovery phase, which begins with the onset of massive diuresis.
Diagnostic Testing: Recognition of exposure to infected rodents is key. Labs will reveal leukocytosis with
left shift and atypical lymphocytes, coagulopathy, thrombocytopenia, elevated liver
enzymes, renal failure, and proteinuria. Serology, polymerase chain reaction (PCR),
and immunohistochemical testing can be performed to confirm the diagnosis.
Treatments: Treatment is supportive. Ribavirin may have some benefit if given early. Endotracheal
intubation with mechanical ventilation and extracorporeal membrane oxygenation
may be necessary.
Pearls: Early treatment in an intensive care unit may be life-saving. Rodent infestation in and
around homes in rural areas is the primary risk for Hantavirus exposure. The disease
is maximal in high rodent years. The Andes Hantavirus can cause person-to-person
transmission.
238
CHAPTER 98 HANTAVIRUS PULMONARY SYNDROME
DV
SNV
Peak: Summer–Fall
AN
AY
B
V V
B CC V NY
Cough
Dyspnea
Fever
Pulmonary
Edema
RIP
40%
Aerosolized
Feces
239
PART 10 RAT-, FLEA-, LOUSE-, AND CHIGGER-BORNE ILLNESSES
Geographic Regions Affected: Southwestern United States, South America, Africa, and Asia
Peak Incidence: In the mid-1300s Yersinia pestis was responsible for The Black Death, a global
pandemic spread by flea-infested rats traveling along trade routes throughout the
known world. Plague has become endemic in certain rural regions such as the
Southwestern United States.
Description: Plague is a zoonotic disease of rodents that is transmitted to humans by the bites of
infected fleas. There are three clinical forms: bubonic, septicemic, and pneumonic,
depending on the route of infection. Bubonic plague is the most common form, caused
by the bite of an infected flea. Y. pestis enters at the bite site and travels through the
lymphatic system to the nearest lymph node, where it replicates and causes painful
lymphadenopathy (bubo). These bubos can ulcerate and become open sores. Septicemic
plague occurs when the infection enters the bloodstream, either directly from flea bites
or secondary to advanced bubonic plague. Pneumonic plague is classified as either
primary or secondary. Primary pneumonic plague is caused by the inhalation of
aerosolized droplets from another person with pneumonic plague, while secondary
pneumonic plague occurs when bubonic plague spreads to the lungs in advanced
disease.
Signs and Symptoms: Bubonic plague is characterized by high fever, chills, weakness, fatigue, and headache
associated with the rapid formation of tender bubo(s). Over time, the bubo(s) may
ulcerate and become suppurative. Patients may develop hypotension, shock, and
disseminated intravascular coagulation (DIC). Blood clots can block small arterioles
and cause acral gangrene, thought to give rise to the term “Black Death.” Septicemic
plague is characterized by the sudden onset of febrile illness without bubo formation.
Nausea, vomiting, and diarrhea can occur. Hypotension and shock develop quickly,
and mortality rates are high. Pneumonic plague is characterized by fever, cough,
dyspnea, and hemoptysis. Lobar consolidation is often present.
Diagnostic Testing: Labs will reveal an elevated white blood cell count (WBC), predominantly immature
neutrophils. Increased BUN/creatinine, elevated liver enzymes, and thrombocytopenia
can occur. Blood cultures are often positive. Diagnosis is confirmed by the identification
of Y. pestis in a sample of fluid from a bubo, blood, or sputum. Serology can be obtained,
and rapid diagnostic test kits exist in some countries.
Treatments: Streptomycin and gentamicin are considered first-line agents. Doxycycline, ciprofloxacin,
and chloramphenicol are also effective treatment options. Doxycycline or ciprofloxacin
can be used as postexposure prophylaxis. A vaccine is available for laboratory and field
workers.
240
CHAPTER 99 PLAGUE
Plague
n i a p esti
(Black Death) rs i
Ye
s
Gr d
Incubation: 2–6 Days am Ro
Death in 10 Days
Weakness/Fatigue
Headache
Septicemic Plague
Nausea/Vomiting
Hypotension Pneumonic Plague
Diarrhea Cough
Shock Dyspnea
Fever/Chills
Hemoptosis
Shock
Bubonic Plague
Bubo
Ulceration
Gangrene
Hematogenous
Spread
Lymphatic Acral
Spread Gangrene
241
PART 10 RAT-, FLEA-, LOUSE-, AND CHIGGER-BORNE ILLNESSES
Reservoir: Rodents, small mammals, domestic animals, and livestock can harbor chronic renal
leptospirosis and excrete bacteria in their urine throughout their lifetime.
Geographic Regions Affected: Worldwide. Endemic in tropical climates with infectious peaks after periods of heavy
rainfall.
Signs and Symptoms: Mild Disease: High fever, chills, headache, myalgia, abdominal pain, nausea, vomiting,
diarrhea, and conjunctivitis. Severe Disease: Characterized by renal failure, hepatic
failure, jaundice, meningitis, myocarditis, cardiac arrhythmia or collapse, and/or
pneumonia with pulmonary hemorrhage.
Diagnostic Testing: Diagnosis is based on a high index of suspicion. IgM and IgG serology can be obtained,
and rapid diagnostic tests are available in some countries. Positive serological tests can
be confirmed with microscopic agglutination testing (MAT).
Treatments: Mild Disease: Oral doxycycline and amoxicillin are effective treatments. Azithromycin
can be used in lieu of doxycycline and has fewer side effects. Severe Disease: Intravenous
(IV) penicillin G or ceftriaxone is required for the treatment of severe disease. Penicillin
can cause Jarisch-Herxheimer reaction. While corticosteroids may have some benefit in
the treatment of severe leptospirosis, further research is required.
Prevention: Chemoprophylaxis with oral doxycycline 200 mg weekly can be considered for people
with a high risk of exposure to leptospirosis.
Pearls: There is an urban legend that leptospirosis has been contracted by a person drinking
from an unwashed soda can contaminated with dried rat urine.
242
CHAPTER 100 LEPTOSPIROSIS
Leptospirosis
90% primary disease only (mild)
to s p i r a s p
10% secondary disease (severe) ep
p
L
Incubation:
4-14 days Spirochete
Headache
Fever Meningitis
chills
Conjunctivitis
Pneumonia
Pulmonary
Hemorrhage
Hepatitis Renal
failure
Myalgia
243
PART 10 RAT-, FLEA-, LOUSE-, AND CHIGGER-BORNE ILLNESSES
Causative Agents: RBF is caused by two different bacteria: Streptobacillus moniloformis in North America
and Spirillum minus in Asia. These bacteria are part of the normal respiratory flora in
rodents.
Reservoir: Rats predominantly, but mice, gerbils, and ferrets can also serve as reservoirs.
Geographic Regions Affected: Streptobacillary RBF has been documented on most continents, but is predominant
in North America. Spirillary RBF is predominantly found in Asia.
Description: RBF is a zoonosis caused by the bite of an infected rodent or through the consumption
of bacterially contaminated food or water.
Signs and Symptoms: Streptobacillary RBF: Short incubation followed by fever, chills, headache, nausea, and
vomiting. A maculopapular rash occurs on the extremities 2–4 days after fever onset
and about 50% of patients will develop polyarthritis. The bite site is typically well
healed and without regional lymphadenopathy. Spirillary RBF: Longer incubation
followed by fever, chills, and ulceration at the bite site with associated lymphangitis and
lymphadenopathy. Arthritis is uncommon and a red-brown macular rash is common
on the face, trunk, and extremities. Haverhill Fever: Fever, chills, rigors, prostration,
myalgia, arthralgia, rash, and severe nausea and vomiting. Mortality for untreated
infections is about 10%.
Diagnostic Testing: Rat-bite fever should be suspected in patients with rash, fever, and arthritis with
known exposure to rats or other reservoir animals. Labs will show leukocytosis with
a shift to the left and mild to moderate anemia. S. moniloformis is difficult to culture
and may be identified on Gram stain as a gram-negative pleomorphic rod. S. minus
cannot be cultured and requires darkfield microscopy or differential staining. A false
positive for syphilis occurs in 25% of cases for S. moniloformis and 50% for S. minus.
Prevention: Avoid rats, specifically in the wild. Proper handling of domestic rodents to avoid
biting behaviors. Handwashing after animal handling and cleaning cages. Rat bites
should be treated prophylactically with antibiotics.
244
CHAPTER 101 RAT-BITE FEVER
Rat-Bite Fever
cillus moni
ba USA
lifo
o
Strept
rm
Rods in Chains
Incubation: 2–10 Days
is
Gram
Spirals
Streptobacillus
p i r ASIA
Incubation: 2–4 Weeks illum minu
s
S
Spirillum
RATS GERBILS
MICE WEASELS
Streptobacilliary Spirillary
• Short Incubation • Longer Incubation
• Arthritis • No Arthritis
• No Adenopathy • Adenopathy
• Maculopapular Rash • Red-brown Macular Rash
245
PART 10 RAT-, FLEA-, LOUSE-, AND CHIGGER-BORNE ILLNESSES
Reservoir: Humans
Description: Trench fever is a zoonotic bacterial infection transmitted via the body louse
classically presenting as a 5-day relapsing fever with associated headache, dizziness,
and shin pain. The disease was most common during WWI trench warfare with
fewer cases reported during WWII. “Urban trench fever” has been reported in
homeless populations.
Signs and Symptoms: After a relatively long incubation period, patients present with fever, retro-orbital
headache, malaise, dizziness, arthralgia, myalgia, splenomegaly, shin pain, and
truncal rash. Fever can be an isolated episode, last for 4–5 days, present as several
episodes of 4–5 days of relapsing fever, or can be persistent for 2–6 weeks’ duration.
Contemporary B. quintana infections are more common in the homeless and HIV/AIDS
population and can present as “urban trench fever,” bacteremia with or without
endocarditis, bacillary angiomatosis, and/or peliosis hepatitis.
Diagnostic Testing: Trench fever should be suspected in homeless individuals or persons with known
exposure to the body louse presenting with shin pain and relapsing fevers. Serology
and blood cultures should be obtained. The bacteria are difficult to culture. Polymerase
chain reaction (PCR), cultures, and immunohistochemical testing should be performed
when endocarditis and/or bacillary angiomatosis is suspected.
Treatments: Effective treatment for patients without endocarditis requires doxycycline daily for
4 weeks and gentamycin daily for 2 weeks. Asymptomatic infections can be treated
with oral doxycycline for 15 days. If bacillary angiomatosis or peliosis hepatitis is
present in patients with AIDS: doxycycline, erythromycin, or azithromycin should be
used for at least 3 months. Endocarditis requires more frequent dosing of gentamycin
and a 6-week duration of doxycycline. Ceftriaxone or another third-generation
cephalosporin may be added for the treatment of endocarditis.
Prevention: Hygiene and avoidance of lice. Patients with pediculosis can be treated with ivermectin
and their clothing and bedding should be washed in hot water and/or treated with
insecticides.
246
CHAPTER 102 TRENCH FEVER
Trench Fever to
n ella quin
t
an
r
Ba
a
Incubation 3–38 Days Gr
Average: 12–25 Days
am Rod
Malaise
“Quintan Fever”
• Isolated
• 4–5 Day Duration
Dizziness • Several Episodes of 5 Days’ Duration
Headache • Persistent for 2–6 Weeks
Fever
Retro-Orbital
Pain Fever
Truncal
Rash
Arthralgia
Splenomegaly
Infection from
Louse Feces
Contemporary Infections
Body Louse #1 • Homeless/HIV/AIDS
• Bacteremia/Endocarditis
• BA (Bacilliary Angiomatosis)
247
PART 10 RAT-, FLEA-, LOUSE-, AND CHIGGER-BORNE ILLNESSES
Geographic Regions Affected: Asia Pacific Rim. Peaks in summer and autumn. Higher incidence in farmers, given
increased exposure to scrub brushes and thus, chiggers.
Description: Scrub typhus is a zoonotic rickettsial-like infection spread by mites (chiggers) common
to farmers in the Pacific Rim exposed to scrub brushes. The geography, clinical picture,
presence of regional lymphadenopathy, and eschars assist in the diagnosis.
Signs and Symptoms: The disease may have a mild prodrome or can occur abruptly. Symptoms can include
fever, chills, headache, diffuse myalgia, and malaise; fever can persist for up to 2 weeks.
Regional lymphadenopathy and characteristic eschars may be identified at the bite
sites and about 50% of patients develop a nonpruritic macular/maculopapular
centrifugal rash that begins on the abdomen and spreads to the face and extremities.
Nausea, vomiting, diarrhea, hepatosplenomegaly, cough, and relative bradycardia can
also occur. The disease may cause multisystemic organ dysfunction and spontaneous
abortion in pregnancy.
Diagnostic Testing: The disease is often diagnosed and treated based on clinical suspicion. Serology is the
most commonly used lab test, and polymerase chain reaction (PCR) testing can be
performed on blood, eschar, or lymph node biopsy. A fourfold increase in IgG in
convalescence is confirmatory.
Prevention: Avoid chiggers and use insect repellants like DEET when traveling in rural areas of
endemic countries.
248
CHAPTER 103 SCRUB TYPHUS
n
Orie
ush
us i
Gr
m
ill
ac
a
Incubation 7–10 Days Co cco b
Peak: Summer & Autumn Chigger-Borne
Farmers
at Risk Headache
Relative
bradycardia Malaise
Cough
Chills
Fever
2 Weeks
Diffuse
Myalgia Lymphadenopathy
Hepatosplenomegaly
Black
Nonpuritic
Eschar
Macular/Maculopapular
Centrifugal Rash Nausea/Vomiting
50% Diarrhea
249
PART 10 RAT-, FLEA-, LOUSE-, AND CHIGGER-BORNE ILLNESSES
Vector: Human Body and Head Louse (Pediculus humanus corporis and capitis)
Geographic Regions Affected: Can occur worldwide; however, most recent cases have occurred in Burundi,
Rwanda, and Ethiopia.
Description: Epidemic typhus is a zoonosis transmitted via the human body or head louse. Recent
cases in the United States have implicated the flying squirrel as a potential animal
reservoir.
Signs and Symptoms: Acute: High fever, chills, headache, confusion, myalgia, cough, dyspnea, tachypnea,
arthralgia, nausea, and abdominal pain occur early in the illness followed by the
appearance of a dark macular/maculopapular, centrifugal rash that spares the face,
palms, and soles. The rash occurs in 64% of individuals after several days of illness.
If untreated, mortality is around 40%. Brill-Zinsser Disease: After years or decades,
individuals with a previous infection and weakened immune system may have a
recrudescence of disease. This occurs in the elderly and mimics the initial infection,
although milder and with a fainter rash. Severe symptoms and death are rare.
Treatments: Effective treatment options include doxycycline twice daily for 1 week or
chloramphenicol four times a day for 5 days.
Prevention: Avoid flying squirrels. Delousing humans, bedding, and clothing can reduce the
transmission of P. humanus. A weekly dose of 200 mg oral doxycycline can be used
as chemoprophylaxis if there is a high likelihood of exposure.
Pearls: Crowding, overpopulation, war, and famine are all linked to an increased incidence
of epidemic typhus.
250
CHAPTER 104 EPIDEMIC TYPHUS
ek
R ic
ii
Oblig
Incubation: 5–23 Days
am
eI
at
Gr
Average: 10–14 Days ntra r
cellula
Rash onset several days
after symptom onset. I’m the U.S.
reservoir!
Chills Chills
Fever Fever
Cough
Dyspnea
Tachypnea
Myalgia Myalgia
Confusion Confusion
Macular/
Maculopapular
Centrifugal
Rash Arthralgia
Arthralgia
Abdominal
Pain
Nausea
Vomiting
Louse-Borne
251
PART 10 RAT-, FLEA-, LOUSE-, AND CHIGGER-BORNE ILLNESSES
Vector: Rat Flea (Xenopsylla cheopis); less commonly, cat and mouse fleas serve as vectors.
Reservoir: Rats
Geographic Regions Affected: Worldwide. U.S. cases have been reported in Texas, California, and Hawaii.
Description: Endemic typhus is a zoonosis transmitted to humans by fleas from infected rats.
Signs and Symptoms: Fever, chills, headache, and myalgia occur early in the illness followed by the
appearance of a faint, maculopapular, centrifugal rash that spares the palms and
soles. The rash occurs in 20% to 50% of individuals after several days of illness.
Nausea, vomiting, diarrhea, and abdominal pain may occur and is more common
in children. Severe disease can cause cough and dyspnea, liver dysfunction, acute
kidney injury, and/or splenomegaly with rupture.
Diagnostic Testing: Labs may reveal thrombocytopenia, hyponatremia, hypoalbuminemia, and increased
liver enzymes. WBC can be normal, elevated, or decreased. Anemia may be present.
The disease is often diagnosed and treated based on clinical suspicion, as serology
mostly confirms the disease in retrospect.
Treatments: Effective treatment options include doxycycline twice daily for 1 week or chloramphenicol
four times a day for 5 days.
Prevention: Rodent control to reduce the number of hosts. Proper flea control measures for
domestic pets, specifically cats.
Pearls: A clinical disease picture similar to endemic typhus has been found to be caused
by Rickettsia felis, carried by cat fleas, with opossums and cats serving as potential
reservoirs.
252
CHAPTER 105 ENDEMIC TYPHUS
R
(Murine Typhus)
i
Oblig
am
eI
at
Gr
Incubation: 1–2 Weeks ntra r
cellula
Rash onset several days Flea-Borne
after symptom onset.
Headache
Severe Disease
Liver Dysfunction
Chills
Fever
20%–50%
Nausea/Vomiting Maculopapular AKI
Centrifugal
Abdominal Pain
Rickettsia Rash
Felis Diarrhea Spares Palms
More Common and Soles
in Children Cough and Dsypnea
Splenic Rupture
Rat Flea
Cat Flea
Rickettsia
Typhi
Rickettsia
Felis
Sread by
Flea Feces
253
PART 10 RAT-, FLEA-, LOUSE-, AND CHIGGER-BORNE ILLNESSES
Viral Hemorrhagic Fevers: Viral hemorrhagic fevers caused by the Arenaviruses are thought to be transmitted to
humans via the excreta of rodents. Lassa is the best understood of these infections
and early treatment with ribavirin is thought to have some benefit.
254
CHAPTER 106 ARENAVIRIDAE
Arenaviridae
ssRNA
Hemorrhagic
Fevers Ar
enaviridae
Argentine HF Junin Virus
Bolivian HF Machupo Virus
Lassa Fever Lassa Virus
Venezuelan HF Guanarito Virus
Brazilian HF Sabia Virus
Chapare HF Chapare Virus
Lujo HF Lujo Virus Lymphocytic
Choriomeningitis
LCM Virus
Aseptic Meningitis
Encephalitis
Meningoencephalitis
Lymphocytes Choroid Plexus
255
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PART 11
OROPHARYNGEAL
INFECTIONS
PART 11 OROPHARYNGEAL INFECTIONS
Incubation: Variable—Patients usually present a few days after initial symptom onset.
Description: Peritonsillar abscess (PTA) is a common soft tissue abscess encountered in clinical
practice that occurs either spontaneously or as the result of untreated tonsillitis.
Signs and Symptoms: Symptoms are often progressive and begin as odynophagia and sore throat on the
ipsilateral (same) side of the infection. Fever, malaise, worsening pain, and ipsilateral
lymphadenopathy and neck pain occur next, as well as halitosis and muffled “hot
potato voice.” Significant illness can present with trismus and/or drooling. Complications
can include Lemierre syndrome, a thrombophlebitis of the internal jugular vein, most
commonly from anaerobic Fusobacterium.
Diagnostic Testing: PTA is often a visual diagnosis. Inspection of the oropharynx will reveal erythema
and swelling of the peritonsillar area and uvular deviation toward the unaffected
side. If trismus is present, a soft-tissue CT of the neck with IV contrast can be
obtained to evaluate for PTA and rule out other types of soft tissue abscesses/deep
space infections. Gram stain and wound cultures can be obtained during drainage or
aspiration of the abscess. Peripheral labs would likely reveal a leukocytosis and
elevated C-reactive protein (CRP).
Treatments: Needle aspiration or incision and drainage are often performed at the bedside by the
EM physician or ENT. Appropriate antibiotics following drainage include penicillin with
or without metronidazole or clindamycin in cases of penicillin allergy. Amoxicillin with
clavulanic acid is often a good antibiotic choice for outpatient management.
258
CHAPTER 107 PERITONSILLAR ABSCESS
Peritonsillar Abscess
(PTA, Quinsy)
Aerobic Anaerobic
Streptococcus Fusobacterium
Staphylococcus Peptostreptococcus
Haemophilus Prevotella
Bacteroides
Symptoms
Fever
Malaise
Odynophagia Hot Potato Voice
Halitosis
Trismus
Lymphadenopathy
Lymph Nodes
259
PART 11 OROPHARYNGEAL INFECTIONS
Geographic Regions Affected: Worldwide. The disease is extremely rare in the United States secondary to vaccinations.
Signs and Symptoms: Some patients may become asymptomatic carriers after exposure.
Tonsillopharyngeal diphtheria: Symptoms are often progressive and begin as
odynophagia, pharyngeal erythema, and sore throat. Low-grade fever, chills,
malaise, fatigue, worsening pain, and lymphadenopathy follow. A characteristic
gray pseudomembrane comprised of white blood cells, fibrin, and dead tissue often
forms. This membrane can potentially spread through the respiratory tract, causing
more significant symptoms.
Nasal diphtheria: Involvement of the nasopharynx is characterized by nasal
congestion and mucopurulent, bloody nasal discharge.
Laryngeal diphtheria: If the pseudomembrane extends down into the larynx,
“diphtheritic croup” can occur, potentially causing respiratory compromise. These
patients will have a barking cough, stridor, hoarseness, significant neck swelling (bull
neck), and may become hypoxic and cyanotic. In addition to localized disease,
diphtheria toxin may spread hematogenously and cause damage to the cardiac,
renal, and/or nervous systems.
Diagnostic Testing: Nasopharyngeal and oropharyngeal cultures should be obtained and plated on Loffler
or Tindale media. Gram stain may reveal gram-positive rods in “Chinese character”
distribution. Polymerase chain reaction (PCR) and enzyme-linked immunosorbent
assay (ELISA) antigen tests can be used to detect diphtheria toxin.
Treatments: Patients should be put on isolation. Antibiotics and horse serum-based antitoxin are
the mainstay of treatment. Antibiotic choices include erythromycin or penicillin for
14 days. Patients are not infectious after 48 hours of antibiotic therapy. The diphtheria
antitoxin can be obtained from the Centers for Disease Control and Prevention
(CDC) and dosing is based on stage and severity of illness.
260
CHAPTER 108 DIPHTHERIA
Diphtheria ac
terium dip
ht
Coryne
h er i
Nasal
ae
Bloody
Gr
c
m
hi
rp
a
Incubation: 2–5 Days Pl e o mo Discharge
Carrier State
261
PART 11 OROPHARYNGEAL INFECTIONS
Description: Herpangina is a viral disease of infants, children, and young adults characterized by
fever and oropharyngeal blister formation. The disease is more common in the
summer and occasionally affects adults.
Signs and Symptoms: Symptom onset is acute and consists of fever, anorexia, malaise, sore throat, headache,
and neck pain. Within 2 days of symptom onset, a viral enanthem appears on the
tonsillar pillars, uvula, soft palate, and posterior pharynx. Lesions may also appear on
the hard palate and tongue. The enanthem typically consists of several (5–10) red
papules that progress to vesicles before ulcerating. Ulcers tend to be less than 5 mm
in size and heal over the course of a week.
Treatments: Supportive. Acetaminophen and/or ibuprofen can be given for pain. Infants unable
to tolerate oral feeding secondary to pain may need intravenous fluids. “Magic
Mouthwash” or a lidocaine swish, gargle, and spit may be used in older patients.
262
CHAPTER 109 HERPANGINA
B
irus
E nte
Incubation: 4 Days
ov
ov
h
r
Duration: 1 Week irus c
71 E
Occurs Mostly in Summer
Fever
Progression
Red Papules
Headache
Vesicles
Superficial Ulcers
2–4mm
Sore Throat
Heals Within 7 days
263
PART 11 OROPHARYNGEAL INFECTIONS
Incubation: Varied
Description: Candidiasis can affect various mucous membranes, including those of the oropharynx,
esophagus, and vagina. Oral candidiasis presents in one of two forms: pseudomembranous
and atrophic. Thrush refers to pseudomembranous oropharyngeal candidiasis and is
common in infants, patients using inhaled corticosteroids, and those with compromised
immune systems (AIDS, immunosuppressants, chemotherapy, etc.) Atrophic or
erythematous candidiasis lacks a pseudomembrane and is more common in older
adults who wear dentures. Antibiotic use is associated with vulvovaginal candidiasis and
esophageal candidiasis is associated with HIV/AIDS.
Signs and Symptoms: While most cases of thrush are asymptomatic, patients may complain of decreased
taste or mild irritation secondary to the pseudomembrane. Atrophic candidiasis can
make it painful to denture wearers. HIV/AIDS patients with thrush complaining of
pain with swallowing (odynophagia) should be screened for esophageal candidiasis.
Diagnostic Testing: Usually a visual diagnosis. The pseudomembrane can be easily scraped off using a
tongue depressor and will cause some mild bleeding. Samples can be sent for KOH
preparation and microscopic examination.
Treatments: Nystatin swish and swallow four times a day is the classic treatment. Clotrimazole
troches placed in the buccal surface of the mouth and allowed to dissolve five times a
day are more effective than nystatin. In cases of failed response to topical treatments,
oral fluconazole can be prescribed.
264
CHAPTER 110 THRUSH
Thrush nd
i d a a l bi c
Ca
an
s
(Oropharyngeal Candidiasis)
Fu n gi
Steroid
Inhalers
Infants
Immunocompromised
265
PART 11 OROPHARYNGEAL INFECTIONS
Description: Strep throat is the most common form of bacterial pharyngitis and peaks in late
winter and early spring. Complications of strep throat can include rheumatic fever,
poststreptococcal glomerulonephritis, and peritonsillar abscess.
Signs and Symptoms: Symptom onset is acute and may consist of fever, anorexia, malaise, sore throat,
headache, abdominal pain, nausea, and vomiting. On examination, patients may
have enlarged tonsils with or without exudate, pharyngeal erythema, oral petechiae,
and enlarged, tender cervical lymphadenopathy. Some patients may develop a
scarlatiniform rash. Cough is notably absent.
Diagnostic Testing: Rapid Strep Test (RADT: Rapid Antigen Detection Test) and throat culture are both
readily available, the latter being the gold standard.
Treatments: The purpose of treatment is to lessen disease severity, reduce transmission, and
decrease the likelihood of complications like rheumatic fever. Penicillins, amoxicillin,
and cephalosporins are effective treatments. Erythromycin, clindamycin, or macrolides
can be used in those patients with penicillin allergies.
Modified Centor Criteria: The Modified Centor Criteria can be applied to estimate the likelihood of strep
pharyngitis. Points are added or subtracted based on risk factors to create a total
score ranging from 21 to 5. The higher the score, the more likely the patient has
strep pharyngitis.
Criteria Interpretation
Exudate 11 0 1–2.5
Age 45 21
266
CHAPTER 111 STREPTOCOCCAL PHARYNGITIS
Streptococcal Pharyngitis
(Strep Throat)
GAS
t re p t o
AS c
oc
G ro u
Incubation: 2–5 Days
cu s
Duration: 3–5 Days
d
Cat
Late Winter/Early Spring
Ro
as
al
e Gram
Not Contagious
24 Hours After Antibiotics
FEVER +1
Headache
ABSENCE OF
COUGH +1
Beefy Red
Enlarged Tonsils Petechiae
AGE EXUDATE +1
<15 + 1
≥45 – 1
Enlarged, Tender
LYMPHADENOPATHY +1
Nausea/Vomiting
Abdominal Pain
267
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PART 12
VIRAL
PART 12 VIRAL
Description: Ebola is viral hemorrhagic fever disease of humans and primates with a high mortality.
Bats are thought to serve as the animal reservoir and humans initially get infected
by consuming bushmeat (bats, gorillas, chimpanzees, shrews, and duikers). Once
infected, human-to-human transmission occurs via contact with infectious blood or
bodily fluids including mucus, feces, vomit, saliva, breastmilk, semen, and possibly
sweat. Blood, vomit, and feces are the most infectious fluids. Dead bodies may also
be infectious, exposing those who prepare and touch the body during burial
ceremonies to risk of infection.
Signs and Symptoms: Initial symptoms are flu-like and include fever, chills, malaise, weakness, headache,
and myalgia. Next, patients develop nausea, vomiting, watery diarrhea, abdominal
pain, and a maculopapular rash. Severe disease can cause renal failure, transaminitis,
disseminated intravascular coagulation (DIC), and hemorrhage. Signs of hemorrhage
include hematochezia, petechiae, bruising, mucosal bleeding, and hematemesis.
Diagnostic Testing: ELISA, IgM/IgG, virus isolation, immunohistochemistry, and polymerase chain
reaction (PCR) tests are available to confirm the diagnosis.
Pearls: There are five species of the Ebola virus genus: Zaire ebolavirus (ZEBOV), Bundibugyo
ebolavirus (BDBV), Tai Forest ebolavirus (TAFV), Sudan ebolavirus (SUDV), and
Reston ebolavirus (RESTV). Ebola viruses are closely related to the Marburg virus,
another filovirus that causes outbreaks of viral hemorrhagic fever.
270
CHAPTER 112 EBOLA
Ebola
o l a Vi r u s
Eb
ss
us
A Fi l ovir
Malaise Headache
Weakness
Fever
Nausea >101.5
Vomiting
Rash
Hematemesis
Renal
Bat
Increased Failure
AST/ALT Duiker
Diarrhea Gorilla
Hematochezia
Myalgia Shrew
Chimpanzee
Source CDC
High Mortality
Burial
Ceremonies
271
PART 12 VIRAL
Reservoirs: Bats, raccoons, skunks, and foxes in the United States; dogs in developing nations.
Incubation: About 1–3 months for most cases. Onset can be delayed for years!
Description: Rabies is a fatal viral zoonosis transmitted from the saliva of infected animals to
humans. After a relatively long incubation period, patients develop an encephalopathy
followed by death. The disease can have one of two presentations, either encephalopathic
(furious rabies) or paralytic (dumb rabies). Encephalopathic rabies is the classic and more
common presentation, notable for hydrophobia (fear of water) and spasms of the
pharynx that occur when the patient attempts to drink water.
Signs and Symptoms: Prodromal symptoms may include fever, headache, malaise, nausea, vomiting, and
pain or paresthesia at the site of the bite. When the virus spreads to the central
nervous system, patients will exhibit one of two clinical presentations of the disease.
Furious Rabies: This is the most common presentation (70%) and includes the classic
findings of hydrophobia, insomnia, confusion, paranoia, anxiety, agitation, and
hallucinations progressing to coma and death. Paralytic Rabies: Presents in 30% of
patients and is associated with an ascending flaccid paralysis, fever, confusion, coma,
and death.
Diagnostic Testing: Direct immunofluorescent staining of skin biopsy specimen, polymerase chain
reaction (PCR) testing of saliva or skin biopsy, and/or detection of anti-rabies virus
antibodies in serum or cerebral spinal fluid (CSF).
Treatments: Supportive. Most patients die within 10 days of the onset of coma. There is a
vaccination series to prevent rabies given as either a preexposure or postexposure
prophylaxis. Preexposure vaccinations are given on days 0, 7, and 21 or 28 and are
recommended for veterinarians, rabies researchers, and some travelers. Postexposure
vaccinations are given on days 0, 3, 7, and 14, with immunocompromised patients
getting a fifth dose on day 28. In addition to vaccination, postexposure prophylaxis
includes weight-based rabies immune globulin on day 0, with half the dose administered
as close to the wound as possible. Those who have received the preexposure vaccination
series do not need immune globulin and should be given booster shots of the vaccine
at days 0 and 3. Proper handwashing and cleaning of any bite wounds with iodine
can help reduce transmission of rabies.
272
CHAPTER 113 RABIES
s
ssR
Incubation 1–3 Months NA u
s
Death Within 10 Days Ly s s a v i r
of Coma
Hypersalivation/Infectious Saliva
Neurologic Symptoms
Insomnia Anxiety 1/2 Immune Globulin
Confusion Agitation Given Near Site of Bite
Paranoia Hallucinations
Skunk
Bat
Raccoon
Fox
Hydrophobia
273
PART 12 VIRAL
Oral Candidiasis: Thrush can occur at any time in HIV-positive individuals, although it is less common
with CD4 counts 500. Incidence increases as CD4 counts become lower (#200), and
recurrent infections are often a sign of HIV disease progression. Treatment options
include oral fluconazole daily for 1–2 weeks, nystatin swish and swallow 4–5 times a
day for 1–2 weeks, or clotrimazole troches 4–5 times a day for 1–2 weeks.
Kaposi Sarcoma: Kaposi sarcoma (KS) is an AIDS-defining illness that can occur with any CD4 count,
although is more common when CD4 counts drop below 250. The cancer is caused
by human herpes virus 8 (HHV-8) and typically presents as red, purple, brown, or black
papular lesions on the skin or mucous membranes. KS and bacillary angiomatosis (BA)
may have similar appearances.
Pneumocystis Pneumonia: Pneumocystis pneumonia is an AIDS-defining illness caused by the yeast-like fungus
Pneumocystis jirovecii. Symptoms of infection include fever, chills, nonproductive cough,
chest pain, and dyspnea. Diagnosis should be suspected in susceptible individuals with the
above symptoms, especially in those with lower CD4 counts. Chest x-ray can be normal
early in the course of disease, but often reveals bilateral, ground-glass, interstitial infiltrates
in a butterfly pattern. Diagnosis is confirmed via sputum sample or broncheoalveolar
lavage. Prophylaxis with TMP/SMX should be initiated in patients with CD4 counts #200.
Sulfa allergic patients can take dapsone, dapsone and pyrimethamine with leucovorin,
aerosolized pentamidine, or atovaquone as alternatives to TMP/SMX. TMP/SMX is the
preferred treatment of active disease, with prednisone added for more severe illness.
274
CHAPTER 114 AIDS: OPPORTUNISTIC INFECTIONS
275
PART 12 VIRAL
276
CHAPTER 114 AIDS: OPPORTUNISTIC INFECTIONS
Mycobacterium Avian Mycobacterium avian complex (MAC) infections are caused by either Mycobacterium
Complex: avium or M. intracellulare and present as either localized or disseminated disease.
Localized disease often presents as lymphadenitis with fever, while disseminated
disease presents as fever with abdominal pain and diarrhea. If a disseminated MAC
infection is suspected, mycobacterial blood cultures should be obtained. Blood
cultures in localized disease will be negative. Primary prophylaxis against MAC
should be started for individuals without active MAC infections and CD4 counts
#50. Preferred agents for prophylaxis include azithromycin or clarithromycin;
rifabutin can be used as an alternative option. Treatment for active infections consists
of azithromycin or clarithromycin plus ethambutol with or without rifabutin.
Bacillary Angiomatosis: BA is the cutaneous manifestation of Bartonella henselae or B. quintana and presents
as red or purplish, nonblanching papules or nodules in HIV-infected individuals.
It can appear similar to KS and may require a biopsy for definitive diagnosis.
Treatment is with erythromycin, doxycycline, or azithromycin.
277
PART 12 VIRAL
ssRNA
Ophthalmic Re
troviridae
CMV Retinitis CD4 ≤50
Candidiasis CNS
Oral CD4 ≤500 Toxoplasmosis
Esophageal CD4 ≤100 CD4 ≤100
Cryptococcus
Pulmonary CD4 ≤100
Tuberculosis
Screen All Patients
Coccidioidomycosis
CD4 ≤250
Bacterial Pneumonia
CD4 ≤200
Pneumocystis
CD4 ≤200
Diarrheal
Histoplasmosis
CD4 ≤150 Isosporiasis CD4 ≤200
Bacillary Angiomatosis
Bartonellosis
CD4 ≤50
278
CHAPTER 114 AIDS: OPPORTUNISTIC INFECTIONS
Miliary
Nodules
Consolidation
Cavitary Mediastinal
Lesion Nodes
Nodule Pleural
Effusion
Tuberculosis
Candidiasis
Screen for
Coccidioidomycosis
when CD4 < 250!
Toxoplasmosis
Coccidioidomycosis
Bacillary
Angiomatosis
Histoplasmosis
279
PART 12 VIRAL
Description: Smallpox is a highly contagious, vaccine-preventable viral disease that was eradicated
from the globe in 1980. The disease was caused by one of two strains of the Variola
virus, either major or minor. Variola major is the more severe of the two, which
causes a higher fever, a more significant rash, and a mortality rate up to 50%. Variola
minor is less severe and carries a mortality rate of ,1%. Smallpox is still studied for
historical purposes and as a potential agent of bioterrorism.
Signs and Symptoms: The classic presentation of smallpox follows several phases and includes a prodrome
consisting of fever, malaise, headache, myalgia, prostration, abdominal pain, nausea,
vomiting, and diarrhea. Next, an enanthem appears in the mouth and on the tongue,
followed by an exanthem starting on the face that spreads in a descending, centrifugal
pattern. All lesions will be at the same stage as the rash progresses from macules, to
papules, to vesicles, to pustules, to scabs. Patients are most contagious early in the
enanthem phase of illness and are no longer contagious once all of the scabs have
crusted over and fallen off. It takes about 3 weeks for the rash to progress from start
to finish.
Diagnostic Testing: Polymerase chain reaction (PCR) testing of lesions and/or blood and serum as per
guidelines from the Centers for Disease Control and Prevention (CDC).
Treatments: Supportive. Patient should be placed in airborne infection isolation room. The CDC
should be contacted for all suspected cases of smallpox.
Smallpox Chickenpox
280
CHAPTER 115 SMALLPOX
Smallpox
riola virus
Va
Pocks
on Trunk More
Pocks on
Less Extremites
Less
More
Rapid
Pocks Development
Slow Deep Superficial Pocks
Development Scar Don’t Scar at Several
Don’t Itch Itch Stages
Pocks
at Same
Stage
Pocks on
Palm & Soles
Less
More (Rare)
Smallpox Chickenpox
281
PART 12 VIRAL
Description: Mononucleosis is a viral disease primarily of adolescents and young adults characterized
by fever, pharyngitis, lymphadenopathy, and extreme fatigue. Mononucleosis is
known as the kissing disease because the virus is transmitted via oral secretions and
can shed into the saliva for several months after initial infection. The disease may
also be spread sexually. When EBV infection occurs in early childhood, it is often
asymptomatic and subclinical.
Signs and Symptoms: A mild prodrome of headache, malaise, and fatigue may precede the classic triad
of high fever, pharyngitis, and lymphadenopathy. Extreme fatigue is common and
may last for months, even after the other symptoms have resolved. Lymphadenopathy
is symmetric and typically involves the posterior cervical chain. Pharyngitis with
exudative tonsillitis is common and is often mistaken for strep throat. If ampicillin
or amoxicillin is prescribed for presumed strep throat, a diffuse maculopapular
rash often occurs. Hepatitis and splenomegaly are common. Splenic rupture can
potentially occur and contact sports should be avoided for at least 3–4 weeks.
Diagnostic Testing: Labs will reveal lymphocytosis with 50% lymphocytes on peripheral smear, with
10% atypical in appearance. Liver enzymes (ALT/AST) are often elevated and
self-limiting. Patients with mononucleosis will produce heterophile antibodies,
which will cause a positive Monospot test. IgM and IgG antibody testing can also be
obtained, as well as EBV DNA polymerase chain reaction (PCR) testing. Clinical
presentation with characteristic CBC findings and a positive Monospot are often
sufficient to make the diagnosis.
Treatments: Supportive.
Pearls: Acute cytomegalovirus (CMV) infection can have a clinical presentation similar to
infectious mononucleosis. In both cases, the illnesses are self-limiting and treatment
is supportive. IgM and IgG antibodies to CMV can be obtained to distinguish it from
EBV infection.
282
CHAPTER 116 MONONUCLEOSIS
Mononucleosis
in-Barr Vi
(Glandular Fever) ste r
Ep
us
(Kissing Disease)
EBV
H H V- 4
Pharyngitis
Often Confused
Lymphadenopathy for Strep Throat
(Posterior Cervical)
Splenomegaly ? Acute
CMV Infection Fever
Monospot
EBV IgG/IgM
≥50% Lymphocytes Extreme Fatigue
≥10% Atypical ALT/AST 50%
283
PART 12 VIRAL
Signs and Symptoms: Most cases of polio (72%) are asymptomatic. Symptomatic infections without central
nervous system (CNS) involvement (24%) are limited to several days of fever, malaise,
headache, fatigue, sore throat, nausea, and vomiting. These mild infections do not
involve the CNS and are referred to as “abortive polio.” When there is CNS involvement
(1%–5% of cases), patients develop an aseptic meningitis several days after the initial
illness. Those patients who make a full recovery from the aseptic meningitis phase are
said to have had non-paralytic polio. In a small percentage of patients with CNS
involvement, there will be selective destruction of motor neurons, resulting in
paralytic polio.
Overall, paralytic polio occurs in ,1% of all infections and presents as spinal,
bulbospinal, or bulbar disease. Spinal polio is the most common form of paralytic
polio and causes an asymmetric weakness of the extremities, affecting the lower
extremities more commonly than the upper extremities. Deep tendon reflexes will
be diminished, while sensation remains intact. Bulbar polio is the least common
form of paralytic polio and can present as dysphagia, dysarthria, dyspnea, and/or
pooling of oral secretions. Bulbospinal polio combines aspects of both bulbar and
spinal polio.
Diagnostic Testing: Polio is often suspected and diagnosed based on clinical presentation. Patients
presenting with signs and symptoms of meningitis should undergo lumbar puncture.
Polymerase chain reaction (PCR) testing can be performed on cerebral spinal fluid
(CSF) to confirm the diagnosis. Serology can also be obtained, comparing acute and
convalescent titers.
Treatments: Supportive.
Pearls: Post-polio syndrome (PPS) is a noncontagious condition that can affect adult survivors
of polio 15–40 years after their initial infection. Symptoms include fatigue, arthralgia,
muscle weakness, and atrophy, occurring in a slow and progressive fashion marked by
long periods of stability.
284
CHAPTER 117 POLIO
Polio
ov
(Poliomyelitis) Poli irus
ssRNA
Incubation: Variable
Non-paralytic: 3–6 Days PV1-PV2-PV3
En
te rovirus
Paralytic: 7–21 Days
Asymptomatic 72%
Bulbar Polio Abortive (Mild) 24%
Dysphasia Aseptic Meningitis 1%–5%
Dysarthria Paralytic <1%
Dyspnea CDC
Pooling Secretions
Virus Infects
Tonsils &
Peyer’s Patches
Bulbarspinal
Polio
Combination of Both
Bulbar & Spinal
Disease
Spinal Polio
Most Common
Asymmetric
Legs > Arms
Fecal-Oral Reflexes
Transmission Sensation Intact
285
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PART 13
PARASITES AND
PRIONS
PART 13 PARASITES AND PRIONS
Vector: Triatomine bugs, also known as reduviid bugs, kissing bugs, blood suckers
Reservoir: Many small and large mammals. In the United States, opossums, raccoons, armadillos,
and rodents are common reservoirs.
Geographic Regions Affected: Endemic in Mexico and Central and South America. States in the southern United States
are potentially at risk (time will tell).
Description: Chagas disease is a tropical parasitic zoonosis caused by the flagellated protozoa
T. cruzi transmitted to humans via the feces of various Reduviid “kissing bugs.”
Chagas disease can also be transmitted congenitally, via blood transfusion, organ
transplantation, or via consumption of food or water contaminated with bug feces.
The disease has acute, intermediate, and chronic phases.
Signs and Symptoms: Acute Phase: Often mild or asymptomatic, but can include fever, malaise, edema,
lymphadenopathy, and hepatosplenomegaly. A chagoma is an acute sign of infection
consisting of localized erythema and edema where the parasites have entered the
skin. Romaña sign is the more classic sign of acute infection and consists of painless
palpebral edema and conjunctivitis 1–2 weeks after the parasites have entered
through the conjunctiva of the involved eye. Once the signs and symptoms of acute
infection have resolved, patients enter an intermediate (latent/asymptomatic) phase
that may evolve into chronic disease years or decades later. Chronic Phase: About one
third of patients will ultimately show signs and symptoms of chronic disease, which
include dilated cardiomyopathy, megaesophagus, achalasia, megacolon, and neuritis.
Diagnostic Testing: Signs, symptoms, and history of travel or residence in an endemic region are
important when considering the diagnosis. Blood smears may reveal the presence
of parasites, but only in the acute phase of the disease. Chronic disease is diagnosed
with serology.
Pearls: Treatment in the United States is only available through the Centers for Disease
Control and Prevention (CDC). There is a consensus that treatment is beneficial for
acute infections, congenital infections, and chronic infections in children. The
treatment of adults with chronic infections is considered on a case-by-case basis.
288
CHAPTER 118 CHAGAS DISEASE
uz
Try
(American Trypanosomiasis)
i
It’s not my kiss that infects
Fl a
ge
oa
him, it’s my feces!
llate oz
d Pr o t
Reduviid
Romaña Sign Kissing Bug
Spread via
Blood Transfusion
Chagoma
Dilated Cardiomyopathy
Hepatomegaly
Megacolon
:
hase
nic P s
Chro Patient
f y
1/3 o myopath
io
Card halasia
ase: Ac n
e Ph acolo
Acut mptoms Meg
S y ths
Mild eks-Mon
t s W e
Las
289
PART 13 PARASITES AND PRIONS
Geographic Regions Affected: West African trypanosomiasis: tropical rainforests in Central and West Africa;
East African trypanosomiasis: savannas and wooded areas in Central, South, and
East Africa.
Signs and Symptoms: Locally, a small chancre may develop within 1–2 weeks at the site of initial infection.
Systemically, the disease progresses through two stages. Stage 1: The hemolymphatic stage
is characterized by flu-like symptoms, headache, malaise, arthralgia, intermittent fever,
and progressive lymphadenopathy. Winterbottom sign (characteristic lymphadenopathy
seen at the back of the neck) is typical for West African trypanosomiasis and may be
seen at this time. Stage 2: The neurologic phase occurs when the parasites penetrate the
blood-brain barrier and is characterized by mood disturbances, insomnia, daytime
somnolence, Parkinson-like symptoms, tremors, ataxia, and various other neurologic
disturbances. Stage 2 illness will progress to coma and death if left untreated.
Diagnostic Testing: Signs, symptoms, and history of travel or residence in an endemic region are
important when considering the diagnosis. Tourists exploring game parks are more
likely to be exposed to East African trypanosomiasis. Microscopy of centrifuged
blood, cerebral spinal fluid (CSF), chancre fluid, and/or lymph node aspirate.
Presence of parasites in CSF confirms stage 2 disease. There are some commercially
available serologic tests.
Treatments: Choice of agent is determined by trypanosome subspecies and stage of disease. Stage
2 disease requires pharmaceutics that can penetrate the blood-brain barrier, all of
which tend to have greater side effects. Medications for each respective stage include
Stage 1: Pentamidine or suramin. Stage 2: Efornithine or melarsoprol or nifurtimox.
290
CHAPTER 119 AFRICAN SLEEPING SICKNESS
Tr y
ei
an
uc
o s o ma br
p
Winterbottom
Sign
Sleep tight,
Tsetse Fly don't let the
Tsetse bite!
Arthralgias
STAGE 1
Tremor
STAGE 2
Hemiparesis
(Paralyzed Limb)
291
PART 13 PARASITES AND PRIONS
Causative Agents: Pediculus humanus capitis (head) and Pediculosis humanus humanus (body)
Lifecycle: The adult head louse is infectious and passed from human to human by close contact,
including the sharing of headbands, hats, combs, and towels. Adult females lay and
attach eggs (nits) to hair shafts close to the scalp. These eggs hatch after 1 week and
release nymphs that go through three molts before becoming adults. Adults are about
2–3 mm long and live for about 30 days. Since head lice need frequent blood meals
to survive, they can only live off of humans for 2 days.
The body louse is very similar to the head louse with a few exceptions. Body lice are
a bit larger (3–4 mm long), live and lay eggs within the seams of clothing or bedding,
and only migrate onto the human to feed. They can live away from a person for
longer (5–7 days) and their eggs take 1–2 weeks to hatch.
Incubation: Variable. It takes several days for head lice to show symptoms and typically longer
for body lice.
Description: Head and body lice are topical ectoparasites that feed on human blood. Head lice
live and lay eggs on hairs of the head near the scalp, whereas body lice live and lay
their eggs in clothing. Head lice are more common in young children and are often
transmitted in school via close contact or during sleepovers. Body lice are common
in homeless populations, colder climates, and conditions of overcrowding.
Signs and Symptoms: The saliva of the louse causes intense itching.
Diagnostic Testing: Diagnosis is made via the visualization of nits (eggs) or lice attached to hair shafts
near the scalp (head lice) or within the seams of clothing (body lice). A magnifying
glass and/or Wood lamp are often helpful in making the diagnosis.
Treatments: For head lice: permethrin, malathion, spinosad, or ivermectin can be used. For body
lice, topical or oral medication is not indicated for the patient. However, clothing and
bedding should be discarded and if not possible, thoroughly washed in hot water and
treated with malathion or permethrin powder.
Pearls: Chronic body lice infestation and subsequent bites can cause thickening and
hyperpigmentation of the skin, particularly around the waistline. This condition is
known as Vagabond disease. Body lice are also known to transmit epidemic typhus,
trench fever, and louse-borne relapsing fever.
292
CHAPTER 120 PEDICULOSIS
Pediculosis
Nits
(Head Lice)
Pediculus
humanus
capitis
(Head Lice)
Nits
(Body Lice)
Pediculus
humanus
humanus
Phthirus
(Body Lice)
pubis
(Pubic Lice)
293
PART 13 PARASITES AND PRIONS
Description: PAM is an extremely rare and highly fatal type of meningoencephalitis caused by the
N. fowleri amebae. These amoebas live freely in warm bodies of freshwater and can
cause PAM if they are inhaled nasally and penetrate the cribriform plate, thus gaining
exposure to the brain and meninges. In most cases, there is a history of recreational
exposure to bodies of warm freshwater preceding illness by several days.
Signs and Symptoms: Symptom onset is acute and similar to bacterial meningitis. Fever, headache, meningeal
signs and symptoms, photophobia, neck stiffness, nausea, vomiting, altered mental status,
and seizures can occur. The disease progresses rapidly, causing increased intracranial
pressure and is often fatal.
Diagnostic Testing: Lumbar puncture is obligatory to make the diagnosis and often reveals an increased
opening pressure. Cerebral spinal fluid (CSF) will reveal a neutrophil-predominant
leukocytosis, erythrocytosis, decreased glucose, and increased protein. Gram stain,
bacterial cultures, and tests for viral causes of meningitis will be negative. Amoebas
may be seen on a wet mount prepared from centrifuged CSF.
Treatments: Given the rarity of the disease, there is no single established treatment protocol, and
Infectious Disease specialists and the Centers for Disease Control and Prevention
(CDC) should be consulted. Some treatment regimens call for amphotericin B,
fluconazole, rifampin, and miltefosine. The CDC should be contacted for guidance
regarding miltefosine, an anti-leishmanial drug that has had benefit against N. fowleri
and other amoeba species.
Pearls: Amoeba is the correct term for a singular organism and amoebas or amebae is
plural. PAM is fortunately quite rare, but often reported on in U.S. media outlets in
the summer months given its high fatality rate. N. fowleri can survive comfortably
in some hot springs and is occasionally found in some regional tap water systems.
Infections in the United States are more common in the summer months (swimming
and water sports) and in the southern states.
294
CHAPTER 121 NAEGLERIASIS
Naegleriasis
(Primary Amoebic Meningoencephalitis)
(Brain Eating Amoeba)
Amoeba
ae
N
le
ri
gler
i a fow
295
PART 13 PARASITES AND PRIONS
Kuru: Kuru is a human prion disease endemic to the Fore people of Papua New Guinea and
was associated with cannibalism. The disease has a long incubation period (averaging
101 years) and causes progressive neurodegeneration, cerebellar ataxia, and myoclonus.
As the disease progresses, patients lose the ability to ambulate and develop dysphagia.
Unable to eat, people would ultimately die from severe malnutrition.
variant Creutzfeldt-Jakob vCJD is considered the manifestation of BSE in humans and occurs when prions
Disease: from infected cows are ingested. It is distinguished from CJD by a younger age of
onset and slower disease progression.
Fatal Familial Insomnia: Fatal familial insomnia is typically an inherited human prion disease, although some
sporadic cases have been reported. Symptoms of the disease tend to manifest
themselves in the mid-50s and include insomnia, mental status changes, confusion, and
hallucinations. Over time, motor symptoms including cerebellar ataxia and Parkinson-like
symptoms occur. Death typically occurs within 3 years of symptom onset.
296
CHAPTER 122 PRION DISEASES
Prion Diseases
Transmissible Spongiform Prion PrP
Encephalopathies
Human Animal
Kuru Bovine Spongiform
Encephalopathy
Creutzfeldt-Jakob
297
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PART 14
BACTERIAL
PART 14 BACTERIAL
Incubation: GI and cutaneous: 1–7 days; Injection: 1–4 days; Inhalation: 1 day–2 weeks
Geographic Regions Affected: Worldwide, rare in the United States and Canada
Signs and Symptoms: Cutaneous: Subcutaneous inoculation of bacterial spores result in local tissue
infection with edema, regional lymphadenopathy, and the formation of a characteristic
black eschar. Inhalation: The inhalation of spores leads to a biphasic illness characterized
by a prodrome of fever, chills, malaise, cough, chest pain, and flu-like symptoms,
followed by the fulminant phase with severe dyspnea, hypoxia, pulmonary edema,
acute respiratory distress syndrome (ARDS), shock, and death. Pleural effusions
and a widened mediastinum secondary to lymphadenopathy on chest x-ray are
characteristic for inhalation anthrax. Gastrointestinal: The consumption of undercooked,
anthrax-infected meat can cause GI disease. The infected parts of the GI tract will
develop edema, inflammation, and ulcerations, and patients will present with nausea,
vomiting, abdominal pain, diarrhea, and possibly, GI hemorrhage. Injection Anthrax:
Outbreaks have occurred in IV drug users injecting heroin. Cutaneous ulcers were
typically absent and hematogenous spread was common. Meningeal: Hematogenous
spread of anthrax can cause hemorrhagic meningitis.
Diagnostic Testing: Gram stain, cultures, polymerase chain reaction (PCR) testing, and serology can be
obtained. Histopathology and immunohistochemistry testing can be performed on
submitted tissue specimens, specifically for those obtained when testing for cutaneous
anthrax.
Pearls: It is illegal to import goat-skin drums from Haiti, given their association with anthrax.
300
CHAPTER 123 ANTHRAX
Anthrax cil
lus anthrac
Ba
is
(Woolsorter Disease)
Spore-Forming
Gr
am Rod
Meningeal
Wide Mediastinum Hematogenous Spread
ARDS
Pulmonary Edema Pulmonary/Inhalation
Fever, Chest Pain, SOB
Most Lethal
Pleural Effusion
Cutaneous
95% Cases
Injection Painless Ulcer
Fever/Chills Black Eschar
Abscess
GI/Intestinal
Nausea/Vomiting
Diarrhea/Abdominal Pain
Spores
301
PART 14 BACTERIAL
Description: Botulism is a rare paralytic illness caused by the toxin produced by the gram-positive,
spore-forming, bacillus-shaped, obligate anaerobic bacteria C. botulinum. Botulism
most commonly occurs as the result of the ingestion of preformed toxin (foodborne)
or spores (infant). In infant botulism, the spores colonize the GI tract and produce
toxin. Other, less common causes of botulism occur secondary to wound infection
(typically from intramuscular or intravenous drug use), spore inhalation, or iatrogenically
(cosmetic Botox).
Signs and Symptoms: Food-borne Botulism: Acute onset bilateral facial palsy and descending weakness in
the absence of fever. Sensation and neurologic status remain intact. Blurry vision,
bradycardia, and GI symptoms such as nausea, vomiting, diarrhea, and abdominal
pain may be present. Infant Botulism: Also known as “floppy baby syndrome.”
Infant may have weak cry, poor feeding, drooling, weakness, and constipation in the
absence of fever. Wound Botulism: Similar presentation to food-borne botulism, but
without GI symptoms. The patient is still exposed to the circulating toxin from the
wound, but their GI tract is spared exposure. Fever may be present, secondary to
the wound infection.
Diagnostic Testing: Patient history, clinical presentation, and electromyogram (EMG) testing suggest
the diagnosis. Infant botulism is confirmed via the isolation of infectious spores and
botulin toxin in stool samples. Food-borne botulism in adults is confirmed via the
detection of botulin toxin in serum, stool, vomitus, or suspect food specimens.
Patients with wound botulism would have detectable toxin in their serum, but not
stool (no GI tract involvement).
Prevention: Use caution with home canning. Discard dented or bulging cans. Do not feed children
less than 1 year of age honey, as it may contain botulism spores.
302
CHAPTER 124 BOTULISM
st
nu
Clo
m
Spore-Forming
Gr
am Rod
Bioterrorism
Inhaled Spores
Food-borne Botulism
Bilateral Facial Palsy
Descending Paralysis
Blurred Vision
Normal Mental Status
Wound Botulism
IM/SQ Black Tar Heroin
Infant Botulism
Floppy Baby
Constipation
Weakness
Poor Feeding
Weak Cry
Drooling
No Fever
Food-borne Botulism
Home Canned Foods
Dented/Buldging Cans
Infant Botulism
Raw Honey
Inhaled Spores
303
PART 14 BACTERIAL
Geographic Regions Affected: Worldwide. More common in the Mediterranean Basin, the Middle East, Eastern
Europe, Asia, Africa, Central and South America.
Signs and Symptoms: Systemic illness has nonspecific symptoms including fever, malaise, weakness, fatigue,
headache, dizziness, myalgia, arthralgia, and night sweats. Localized infections can
occur almost anywhere, with bone and joint involvement the most common.
Examples of localized infection include sacroiliitis, epididymo-orchitis, pneumonia,
hepatitis, endocarditis, uveitis, dermatitis, and meningitis. Symptoms of localized
infection are dependent on affected organ system. Brucellosis is considered chronic
when symptoms last for more than a year. Disease may reoccur or relapse if antibiotics
are discontinued prematurely.
Diagnostic Testing: Culture, serology, and polymerase chain reaction (PCR) testing. Since Brucella is
difficult to grow, the laboratory should be alerted when specimens are submitted for
culture.
Treatments: Nonfocal, uncomplicated brucellosis can be treated with gentamycin daily for 7 days
combined with doxycycline twice daily for 6 weeks or rifampin daily combined with
doxycycline twice daily for 6 weeks. Alternative regimens include the combination of
ciprofloxacin with doxycycline or rifampin. Specific treatment regimens exist for
localized infection (spondylitis, sacroiliitis, endocarditis, and meningitis) and for
infections during pregnancy.
Pearls: Grandpa Kloss was a dairy worker in New Jersey, loved to drink raw buttermilk to
quell his peptic ulcer disease, and subsequently developed brucellosis “undulant
fever” as a result.
304
CHAPTER 125 BRUCELLOSIS
Brucellosis Bru
cella spp
.
(Mediterranean Fever)
cillus
(Malta Fever)
Gram
(Undulant Fever)
oba
In
cc
t ra o
cell ular C
Fever Fatigue
Headache
B. melitensis
Pneumonia
Night Endocarditis
B. suis Sweats
Hepatitis
Weakness
B. abortus
Sacroiliitis Arthralgia
Epididymo-orchitis
B. canis
Spontaneous
Abortion
Myalgia
Undulant fever
305
PART 14 BACTERIAL
Geographic Regions Affected: Worldwide—Most common in developing nations. The vast majority of U.S. cases
have been linked to travel to endemic countries (about 75%–80%).
Description: Typhoid fever is systemic bacterial illness characterized by abdominal pain and fever
caused by the gram-negative, flagellated, rod-shaped bacteria Salmonella enterica
serotype Typhi. Paratyphoid, a similar illness, is caused by S. enterica serotype
Paratyphi A, B, or C.
Signs and Symptoms: Typhoid classically goes through several phases, each lasting about a week. Symptoms
during the first week include progressive fever, chills, malaise, relative bradycardia,
headache, and cough. In the second week of illness, severe fatigue, abdominal pain,
delirium, and a characteristic rash consisting of salmon-colored “rose spots” appear
on the chest and abdomen. Constipation or diarrhea can also occur, as well as
hepatosplenomegaly. In the third week of illness, severe complications such as
encephalitis and gastrointestinal (GI) hemorrhage or perforation can occur. Convalescence
typically begins after the third week of illness and it may take several months for the
patient to fully recover.
Diagnostic Testing: Culture and serological testing. Cultures can be obtained from blood, stool, duodenal
aspirates, vomitus, rose spots, and bone marrow. Multiple sets of blood cultures
increase the likelihood of detection.
Treatments: Ciprofloxacin or levofloxacin can be used for treatment of cases of typhoid fever
that were not acquired in Asia. Given increasing resistances to fluoroquinolones
in Asia, ceftriaxone or azithromycin should be used for infections linked to that
region. Azithromycin can be used in children. Dexamethasone is indicated as an
adjunct in cases of severe infection.
Prevention: Oral and intramuscular (IM) typhoid vaccines are available in the U.S. for travelers
to endemic areas.
Pearls: Typhoid Mary, AKA Mary Mallon, was the first person in the United States identified
as an asymptomatic carrier of S. enterica serotype Typhi. She worked as a cook in
upper-class homes and is presumed to have infected more than 50 people. After
outbreaks of typhoid occurred in her place of employment, she would quit and move
on, often changing her name and inadvertently infecting others. She spent the last
years of her life under forced quarantine.
306
CHAPTER 126 TYPHOID FEVER
Typhoid Fever l la
one ent
m Typhi e
(Enteric Fever)
ric
l
Sa
a
d
Gra
Ro
d
Fl a g e l l a t e
m
Incubation: 6–30 Days
Delerium
Constipation/Diarrhea
Hepatosplenomegaly
GI Bleed
GI Perforation
Fecal-Oral
Transmission Chronic Carriers
307
PART 14 BACTERIAL
Vector: Cat flea (Ctenocephalides felis)—Fleas transmit the bacteria between cats.
Reservoir: Cats are the natural reservoir, with kittens more likely to carry the bacteria.
Signs and Symptoms: In the vast majority of cases, a small papule or nodule forms at the inoculation site
followed by the development of ipsilateral regional lymphadenopathy. Patients may
also present with low-grade fever, malaise, and headache. Arthralgia, myalgia, and
arthritis can also occur. Meningitis, osteomyelitis, and endocarditis can occur, but
are rare. Ocular manifestations can include parinaud oculoglandular syndrome, a
granulomatous conjunctivitis with preauricular lymphadenopathy. Immunocompromised
(HIV1/AIDS) patients are at risk of developing peliosis hepatis and/or bacillary
angiomatosis (BA).
Diagnostic Testing: Labs may reveal mild leukocytosis, predominantly neutrophils, and an elevated
erythrocyte sedimentation rate (ESR). IgM and IgG antibodies can be obtained.
Prevention: Flea control for cats, hand washing after contact with cats or cat feces, and keeping
cats indoors to limit exposure to fleas.
Pearls: Bacillary angiomatosis (BA) may be mistaken for Kaposi sarcoma and vice versa.
308
CHAPTER 127 CAT SCRATCH FEVER
lae
Ba
Incubation: 1–2 Weeks
ria
Gra
m
te
c
Papule at Inoculation Site Pr o t e o b a
Often Self-limiting
Papule
(Initial Infection)
Peliosis Hepatis Osteomyelitis
(Immunocompromised) (Rare)
Arthritis/Arthralgia
More Common
From Kittens
309
PART 14 BACTERIAL
Reservoir: Armadillos
Geographic Regions Affected: India, Brazil, and Indonesia have the highest incidence.
Description: Leprosy is an infection of the skin, nasal mucosa, and cutaneous nerves caused by
the slow-growing, gram-positive, intracellular bacteria M. leprae. There are several
ways to categorize leprosy, with the World Health Organization’s (WHO) classification
being the simplest. The WHO classifies the disease as paucibacillary (tubercular)
when there are five or fewer skin lesions or multibacillary (lepromatous) when there
are six or more lesions. Multibacillary leprosy is a more severe presentation found in
patients with a weaker immune response to the infection. Despite long-held historical
beliefs, leprosy is not very contagious.
Signs and Symptoms: Cutaneous skin lesions, neuromas, and sensory loss are hallmarks of the disease.
Hypopigmented skin patches, decreased sensation, paresthesias, muscle weakness,
thickened earlobes, loss of eyebrows and eyelashes, nasal perforation, saddle nose,
and corneal scaring leading to blindness can occur. Diminished sensation can lead to
burns or wounds on the palms and soles. In more severe disease, auto-amputation of
digits, peroneal, tibial, and ulnar neuropathy may be seen.
Diagnostic Testing: Skin biopsies and polymerase chain reaction (PCR) testing can be performed to
confirm the diagnosis.
Treatments: Dapsone was used for many years as a single agent to treat leprosy until resistance
emerged. Multidrug therapy is now required, often for 6–12 months or longer. There
are two current treatment protocols, one put forth by the World Health Organization
(WHO) and another by the National Hansen’s Disease Program. According to the
WHO protocol, paucibacillary leprosy is treated with dapsone and rifampicin for
6 months and multibacillary leprosy is treated with dapsone, rifampicin, and
clofazimine for 12 months.
Pearls: The bacteria that carries leprosy reproduces at cooler temperatures, thus disease is
limited to the skin and cutaneous nerves in humans. Since armadillos have a lower
core body temperature than most mammals, they serve well as a natural reservoir.
M. leprae, like the mycobacterium that causes tuberculosis (TB), has a waxy outer
layer.
310
CHAPTER 128 LEPROSY
Leprosy
acterium le
(Hansen Disease) ob
pr
c
My
ae
hic
I nt
G
Incubation: 9 Months – c e r a m R o do
ra
rp
llul
ar Plem
20 Years
Average: 5 Years Skin Nodules
Loss of Eyelashes/Eyebrows
Blindness Thickened Earlobes
(Corneal Scaring) Saddle Nose
Nasal Perforation
Hypopigmented
Patches
Claw Hand
(Radial Ulnar Neuropathy)
Armadillos
Muscle Weakness
Claw Toes
(Posterior Tibial Neuropathy)
Drop Foot
(Common Peroneal Neuropathy)
311
PART 14 BACTERIAL
Description: Infective endocarditis is an infectious process of the inner lining of the heart, mostly
of the heart valves, typically caused by bacteria (bacterial endocarditis [BE]). The
disease may have a short incubation period and present acutely (acute BE) or may
have a more insidious and indolent course of progression and develop over several
weeks (subacute BE).
Risk Factors: Intravenous (IV) drug abuse, poor dentition, valvular heart disease, congenital heart
disease, prosthetic heart valves, indwelling lines, pacemakers, past history of infective
endocarditis, and chronic hemodialysis.
Signs and Symptoms: Fever is the most common presenting symptom (up to 90%) and is often associated
with chills, fatigue, and malaise. A heart murmur is present in up to 85% of patients.
Patients may also develop myalgia, arthralgia, splinter hemorrhages, septic emboli,
petechiae, splenomegaly, cough, weight loss, and/or glomuleronephritis. Janeway
lesions, Osler nodes, and Roth spots are highly suggestive of bacterial endocarditis.
Definitions: Janeway lesions are nontender erythematous macules on the palms and soles.
Osler nodes are painful, purplish-red lesions found on the pads of the fingers.
Roth spots are retinal hemorrhages with pale centers.
Diagnosis: Bacterial endocarditis should be considered when patients with any of the above risk
factors present with fever, heart murmur, and clinical signs and/or symptoms supporting
the diagnosis. Blood cultures should be obtained from at least three different sites and an
echocardiogram, preferably transesophageal, should be performed looking for valvular
vegetations. Labs may show elevated C-reactive protein (CRP), erythrocyte sedimentation
rate (ESR), and rheumatoid factor.
Treatments: Empiric treatment should be initiated in acutely ill patients once blood cultures have
been obtained. Vancomycin and ceftriaxone or gentamycin are good first-line agents
until a more tailored regimen can be provided based on blood culture results. If patients
are not acutely ill or in heart failure, treatment can be withheld until blood cultures are
resulted. If the initial round of blood cultures is negative in suspect patients, two to three
more sets should be drawn prior to the initiation of empiric treatment.
312
CHAPTER 129 INFECTIVE ENDOCARDITIS
Chills
Heart
Murmurs
= 85%
Roth Spots
(Retinal Hemorrhages)
Vegetations
Pacemaker
Indwelling
Lines
Petechiae
Echocardiogram
Artificial
IV Drug Use
Valves
Janeway
Lesions
Osler
Arthralgia Nodes
Myalgia
Splinter
Hemorrhages
Janeway
Lesions
313
PART 14 BACTERIAL
Geographic Regions Affected: Worldwide—More common in developing nations, where mass vaccination with
tetanus toxoid is less common.
Signs and Symptoms: Generalized Tetanus: This is the most common form of tetanus (about 80%) and
often presents as trismus or risus sardonicus with muscle spasms that develop in a
descending pattern. Patients may develop sympathetic hyperactivity, laryngospasm,
and opisthotonus (clenched fists, flexed arms, arched back, and extended legs).
Mortality is around 10%–20%. Localized Tetanus: This is a mild form of tetanus with
localized muscle spasm in close proximity to the wound. It is more common in
partially immunized patients and has a low mortality. Neonatal Tetanus: This form of
tetanus has the highest mortality and results from the contamination of the infant’s
umbilical stump with dirt or bacteria-laden matter. Infants first exhibit poor feeding
and later progress to full-blown tetanus. Cephalic Tetanus: This is the rarest form of
the disease, has a short 1–2 day incubation period, and results from a head or neck
wound. Unlike the other forms that cause muscle spasm/tetany, cephalic tetanus
commonly presents as unilateral facial nerve palsy.
Diagnostic Testing: Tetanus tends to be a clinical diagnosis based on clinical findings and a history of
wound infection in an unvaccinated or undervaccinated patient.
Treatments: Tetanus immune globulin should be given to sequester unbound toxin and vaccination
with tetanus toxoid should be initiated. Wound debridement, wound care, and
antibiotic administration should also be performed. Patients may require intubation
to secure the airway and provide ventilation. Benzodiazepines and/or neuromuscular
blocking agents can be given for muscle spasm.
314
CHAPTER 130 TETANUS
Tetanus
um te
(Lockjaw) tridi ta
os
Cl
ni
d
Gra
m
Ro
c
A n a erobi
Generalized Tetanus
(Most Common)
Lockjaw (Trismus)
Wound
Risus Sardonicus
Sympathetic
Overactivity
Descending Progression
Localized Tetanus
(Mild Form/Low Fatality)
Opisthotonus
Neonatal Tetanus
(High Mortality)
Ptosis
Facial
Paralysis
Cephalic Tetanus
(Rare)
315
PART 14 BACTERIAL
Signs and Symptoms: Gastroenteritis: Fever, nausea, vomiting, diarrhea, headache, and myalgia are
common symptoms. Invasive Disease: Pregnant women with listeriosis may become
bacteremic and develop fever, chills, back pain, myalgia, and other flu-like symptoms.
Passage of the bacteria to the fetus in utero may result in premature birth, miscarriage,
and/or stillbirth. Infants infected in utero may be born with sepsis or granulomatosis
infantiseptica, a severe infection characterized by numerous abscesses throughout
the infant’s internal organs. Those infants infected at birth via asymptomatic vaginal
infections may develop meningitis and/or sepsis. The immunocompromised,
including those at extremes of age, are at higher risk of invasive disease and may
present with fever, chills, myalgia, sepsis, meningoencephalitis, and/or sepsis.
Cutaneous and ocular infections have been occasionally reported in veterinarians
and farmers.
Diagnostic Testing: Positive blood or cerebral spinal fluid (CSF) cultures will confirm the diagnosis.
Pearls: Mortality rate from invasive disease ranges between 20% and 30%. Listeriosis in
pregnancy is most common in the third trimester and often has a mild flu-like
presentation with fever, myalgia, and back pain. Blood cultures for febrile pregnant
women should be obtained when listeria is suspected and/or there is no other
explanation for the febrile illness.
316
CHAPTER 131 LISTERIOSIS
ge
r
(Listeria)
Li ste
nes
Gra
m R od
Incubation: Varied
Pregnant
No
ese
w
R
he
C
a
Mi
lk / No Young
Listeriosis
GI Nausea
Fever
Vomiting
Myalgia
Diarrhea
Neonatal
Pregnant Flu-like Symptoms
Meningitis Female Possible Miscarriage
( 30% of cases) Possible Stillbirth
Infection of Sepsis
Newborns Meningitis
Granulomatosis infantiseptica
2011
Cantelope
Outbreak 30%
RIP
Rate
Young
Cheese
317
PART 14 BACTERIAL
Description: Q fever is a human bacterial zoonosis caused by the gram-negative, obligate intracellular,
spore-forming Coxiella burnetii. It is carried by sheep, cattle, and goats and can be
transmitted to humans through exposure to bacterial spores or infectious bodily
fluids. The disease can have one of several presentations, including a mild flu-like
illness, pneumonia, hepatitis, or endocarditis. Its spores can be used as an agent of
bioterrorism.
Signs and Symptoms: Flu-like Illness: This is the most common manifestation and presents as acute fever,
chills, malaise, fatigue, headache, and diaphoresis. Fever can last for 2–3 weeks.
Pneumonia: Patients may develop a mild pneumonia with nonspecific chest x-ray
findings. Dyspnea, pleuritic chest pain, and nonproductive cough are common.
Arthralgia and myalgia may also occur. Hepatitis: Transaminitis, fever, hepatomegaly,
and granulomas on liver biopsy are typical findings. Additional gastrointestinal (GI)
symptoms can include nausea, vomiting, and, less commonly, diarrhea. Endocarditis:
Acute or chronic endocarditis can occur, with chronic endocarditis more common in
the immunocompromised and those with preexisting valvular abnormalities.
Diagnostic Testing: Polymerase chain reaction (PCR) testing can be performed on blood or serum in the
first 2 weeks of infection and prior to antibiotic administration. IgM/IgG levels can
be obtained. A fourfold rise of IgG levels in convalescence is confirmatory.
Treatments: Doxycycline is the first-line agent. TMP/SMX can be used in children or pregnant
women. Endocarditis is very difficult to treat and requires doxycycline and
hydroxychloroquine for 18–36 months or doxycycline and a fluoroquinolone
for 2–4 years.
Pearls: Relapse can occur after discontinuation of treatment; if so, treatment should be
resumed.
318
CHAPTER 132 Q FEVER
Q Fever xie
lla burne
Co
tii
lar
Gra m
ellu
Incubation: 2–3 Weeks
ac
Ob r
Can Become Chronic l i g a t e I nt
Headache
Animal Workers
Fever
Flu-like
Illness
Pneumonia Cough
Inhaled
Spores
Myalgia Semen
Vaginal Mucus
Granulomatous
Hepatitis
Endocarditis
Arthralgia Feces
Urine
E
R FAR
WA
BIO
319
PART 14 BACTERIAL
Signs and Symptoms: Symptoms vary based on organ system involved. Pneumonia is the most common
disease manifestation and presents as fever, chills, malaise, headache, anorexia, and
cough. Cutaneous disease includes skin abscesses and ulcerations. Bacteremia can
lead to sepsis, pneumonia, or disseminated disease. Genitourinary infections,
osteomyelitis, septic arthritis, parotitis, hepatic abscesses, and splenic abscesses may
also occur. Chronic pulmonary infections may mimic tuberculosis (TB).
Diagnostic Testing: Cultures of blood, sputum, urine, and cutaneous ulcers should be obtained. Gram
stain and microscopy may reveal the bacteria, which has a bipolar “safety pin”
appearance. Serology and polymerase chain reaction (PCR) are of little benefit in
diagnosis.
Treatments: Two stages of treatment are required: intravenous antibiotics such as ceftazidime or
meropenem are typically given for 10–14 days followed by doxycycline and TMP/SMX
orally for 3–6 months.
Pearls: The authors dedicate this illustration to Mike Cadogan, MD, our EM colleague in
the great Down Under. Please check out his Life in the Fast Lane Medical Blog.
Melioidosis is endemic in northern Australia.
320
CHAPTER 133 MELIOIDOSIS
Melioidosis
ria pseud
(Pseudoglanders) lde
om
o
Burkh
(Whitmore Disease)
allei
Gra
Incubation: 1–21 Days
ng
m i
ni
Average: 9 Bipolar Sta
10% Become Chronic
Symptoms >2 months
= Chronic Infection
Pneumonia
Fever
Abscess
Diabetes
(Risk Factor)
Liver Abscess
Splenic Abscess
Septic
Arthritis I’m rarely
affected!
www.lifeinthefastlane.com
321
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Sanford Guide to Antimicrobial Therapy. 46th ed. The Sanford Guide to Antimicrobial Therapy. 46th ed.
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Walters KH, Traxler RM, Marston CK. Anthrax. In: Brunette Judd MC, Mintz ED. Typhoid & Paratyphoid Fever. In:
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Levine DP, Brown PD. Infections in Injection Drug Users. In:
Schwartzman WA. Cat scratch disease and other Barton- Bennett JE, Dolin R, Blaser MJ, eds. Principles and Practice of
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TETANUS
LEPROSY
Gilbert DN, Chambers HF, Eliopoulos GM, et al., eds.
Castro-Echeverry E, Lee T, Vandergriff T, Cockerell CJ. The Sanford Guide to Antimicrobial Therapy. 46th ed.
Leprosy. In: Schlossberg D, ed. Clinical Infectious Disease. Sperryville, VA: Antimicrobial Therapy Inc; 2016.
2nd ed. Cambridge, United Kingdom: Cambridge University
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Bennett JE, Dolin R, Blaser MJ, eds. Principles and Practice of
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Sperryville, VA: Antimicrobial Therapy Inc; 2016.
Percak JM, Hasbun R. Myelitis and peripheral neuropathy.
National Hansen’s Disease (Leprosy) Program Caring In: Schlossberg D, ed. Clinical Infectious Disease. 2nd ed.
and Curing Since 1894 | Official web site of the U.S. Cambridge, United Kingdom: Cambridge University Press;
Health Resources & Services Administration. Available at: 2015:510-523.
https://www.hrsa.gov/hansens-disease/index.html. Accessed
October 6, 2017. Tiwari TSP. Tetanus. In: Brunette GW, ed. CDC Yellow
Book 2018 Health Information for International Travel.
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the U.S. Health Resources & Services Administration. 325-326.
Available at: https://www.hrsa.gov/hansens-disease/diagnosis/
recommended-treatment.html. Accessed October 6, 2017.
LISTERIOSIS
Renault CA, Ernst JD. Mycobacterium leprae (Leprosy). In:
Bennett JE, Dolin R, Blaser MJ, eds. Principles and Practice Gilbert DN, Chambers HF, Eliopoulos GM, et al., eds. The
of Infectious Diseases. 8th ed. Philadelphia: Elsevier Saunders; Sanford Guide to Antimicrobial Therapy. 46th ed. Sperryville,
2015:2819-2831. VA: Antimicrobial Therapy Inc; 2016.
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Lorber B. Listeria. In: Schlossberg D, ed. Clinical Infectious of Infectious Diseases. 8th ed. Philadelphia: Elsevier
Disease. 2nd ed. Cambridge, United Kingdom: Cambridge Saunders; 2015:2208-2216.
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Gilbert DN, Chambers HF, Eliopoulos GM, et al., eds. Boggild AK, Wilson ME. Recreational water exposure. In:
The Sanford Guide to Antimicrobial Therapy. 46th ed. Schlossberg D, ed. Clinical Infectious Disease. 2nd ed.
Sperryville, VA: Antimicrobial Therapy Inc; 2016. Cambridge, United Kingdom: Cambridge University Press;
2015:800-809.
Holtom PD. Rickettsial infections. In: Schlossberg D, ed.
Clinical Infectious Disease. 2nd ed. Cambridge, United Currie BJ. Burkholderia pseudomallei and Burkholderia
Kingdom: Cambridge University Press; 2015:1093-1097. mallei: Melioidosis and Glanders. In: Bennett JE, Dolin R,
Blaser MJ, eds. Principles and Practice of Infectious
Kersh GJ. Q Fever. In: Brunette GW, ed. CDC Yellow Book Diseases. 8th ed. Philadelphia: Elsevier Saunders; 2015:
2018 Health Information for International Travel. Oxford, 2541-2551.
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Gilbert DN, Chambers HF, Eliopoulos GM, et al., eds.
Marrie TJ, Raoult D. Coxiella burnetii (Q Fever). In: The Sanford Guide to Antimicrobial Therapy. 46th ed.
Bennett JE, Dolin R, Blaser MJ, eds. Principles and Practice Sperryville, VA: Antimicrobial Therapy Inc; 2016.
INDEX
A Amoxicillin
AASLD, recommendations for patients with hepatitis B, 4t with clavulanic acid, for peritonsillar abscess, 258t
Abdominal pain for leptospirosis, 242t
in Ebola, 270t for Lyme disease, 86t
in endemic typhus, 252t for strep throat, 266t
in epidemic typhus, 250t Amphotericin B
in smallpox, 280t for blastomycosis, 156t
in strep throat, 266t for histoplasmosis, 158t
Abscesses for naegleriasis, 294t
amebic liver, 48t for paracoccidioidomycosis, 152t
peritonsillar, 257–259, 258t, 259f for sporotrichosis, 150t
skin, in melioidosis, 320t Anal itching (pruritus ani), 112t
tubo-ovarian, 170t Anaplasma phagocytophilum, 80–81t, 90t
Acetaminophen Anaplasmosis, 90f, 80–81t, 90–91, 90t
for dengue fever, 220t Ancylostoma braziliense, 124t
for erythema infectiosum, 58t Ancylostoma duodenale, 116t
for herpangina, 262t Ancylostomatidae, 124t
for yellow fever, 222t Andes virus (ANDV), 238t
Active trachoma, 180t Anemia, B12 megaloblastic, 132t
Acute form, of paracoccidioidomycosis, 152t Animal blood, infected, during slaughter/butchering, 96t
Acute infection, of coccidioidomycosis, 154t Anogenital warts, 172t. See also Condylomata acuminata
Acute schistosomiasis, 142t Anopheles spp., malaria and, 224–225t
Acyclovir Anorexia
for chickenpox, 62t in herpangina, 262t
for herpes simplex, 184t in strep throat, 266t
Adamantanes, for influenza, 212t Anthrax, 299–301, 300t, 301f
Adrenal insufficiency, in paracoccidioidomycosis, 152t Antibiotics
Aedes aegypti, Zika virus and, 218t for campylobacteriosis, 24t
Aedes albopictus, Zika virus and, 218t for cholera, 22t
Aedes spp., 220t for group B Streptococcus, 64–66t
chikungunya and, 232t for pertussis, 68t
yellow fever and, 222t for reactive arthritis, 182t
Aedes triseriatus, mosquito-borne encephalitis and, for salmonellosis, 20t
228–230t for shigellosis, 18t
African sleeping sickness, 290–291, 290t, 291f topical, for dracunculiasis, 122t
Agar plate method, in threadworm, 126t for vibriosis, 34t
Agitation, furious rabies and, 272t for yersiniosis, 30t
AIDS Antibody detection by ELISA (IgG and IgM), for Crimean-Congo
congenital and perinatal infections in, 64–66t hemorrhagic fever, 96t
cryptosporidiosis in, 46t Antigen-capture enzyme-linked immunosorbent assay, for
opportunistic infections in, 274–279, 274–277t, 278f Crimean-Congo hemorrhagic fever, 96t
Albendazole Anxiety, furious rabies and, 272t
for ascariasis, 104t Arenaviridae, 254–256, 254t, 255f
for cutaneous larva migrans, 124t Argentine hemorrhagic fever, 254t
for hookworm, 116t Armadillos, leprosy and, 310t
for pinworms, 112t Arthralgia
for trichinosis, 120t in chikungunya, 232t
for whipworm, 118t in epidemic typhus, 250t
Allergic bronchopulmonary aspergillosis (ABPA), 164t, in Haverhill fever, 244t
165f in trench fever, 246t
Alveolar echinococcosis (AE), 186. See also Dog tapeworm Arthritis
Amebiasis, 48–50, 48t, 49f reactive, 182–183, 182t, 183f
Amebic liver abscesses, 48t in spirillary rat-bite fever, 244t
American tick fever. See Colorado tick fever Arthrocentesis, for reactive arthritis, 182t
American trypanosomiasis. See Chagas disease Arthroconidia, in coccidioidomycosis, 154t
349
350 INDEX
C Chest X-ray
Calamine lotion, for chickenpox, 62t for bronchiolitis, 72t
Calcofluor staining for coccidioidomycosis, 154t
for coccidioidomycosis, 154t for croup, 76t
for paracoccidioidomycosis, 152t for histoplasmosis, 158t
Campylobacter coli, 24t for psittacosis, 208t
Campylobacter jejuni, 24t for severe acute respiratory syndrome, 214t
Campylobacter spp., reactive arthritis due to, 182t for tuberculosis, 204t
Campylobacteriosis, 24–25, 24t, 25f Chickenpox, 62–63, 62t, 63f
Candida albicans, causing thrush, 264t in congenital and perinatal infections, 64–66t
Candida vulvovaginitis, 194t, 195f Chikungunya, 232–234, 232t, 233f
Candidal stomatitis. See Thrush Children
Cantharidin, for molluscum contagiosum, 196t giardiasis in, 44t
Carcinoma hand, foot, and mouth disease in, 70t
biliary ductal, 144t rotavirus in, 40t
hepatocellular Chills
hepatitis B and, 4t in Ebola, 270t
hepatitis C and, 8t in endemic typhus, 252t
Cat scratch disease. See Cat scratch fever in epidemic typhus, 250t
Cat scratch fever, 308–309, 308t, 309f in Haverhill fever, 244t
Catarrhal stage, of pertussis, 68t in scrub typhus, 248t
Cattle in spirillary rat-bite fever, 244t
anthrax and, 300t in streptobacillary rat-bite fever, 244t
beef tapeworm and, 134t Chinese liver fluke. See Liver fluke
Q fever and, 318t Chlamydia, 178–179, 178t, 179f
Cave disease. See Histoplasmosis in congenital and perinatal infections, 64–66t
Cefotaxime, for vibriosis, 34t Chlamydia pneumoniae, reactive arthritis due to,
Ceftazidime, for melioidosis, 320t 182t
Ceftriaxone Chlamydia psittaci, 208t
for chancroid, 190t Chlamydia trachomatis, 178t
for chlamydia, 178t lymphogranuloma venereum due to, 198t
for endocarditis, 246t reactive arthritis due to, 182t
for gonorrhea, 170t trachoma due to, 180t
for infective endocarditis, 312t Chloramphenicol
for leptospirosis, 242t for endemic typhus, 252t
for Lyme disease, 86t for epidemic typhus, 250t
for syphilis, 176t for plague, 240t
for typhoid fever, 306t for Rocky Mountain spotted fever, 84t
for vibriosis, 34t for scrub typhus, 248t
Cefuroxime, for Lyme disease, 86t for tularemia, 94t
Central Asian hemorrhagic fever. See Crimean-Congo hemorrhagic fever Chloroquine phosphate, for malaria, 224–225t
Centrifugal rash Cholera, 22–23, 22t, 23f
in endemic typhus, 252t Chronic cavitary disease, in histoplasmosis, 158t
in epidemic typhus, 250t Chronic disease, of paracoccidioidomycosis, 152t
Cephalic tetanus, 314t Chronic pulmonary infections, in melioidosis, 320t
Cephalosporins Chronic symptoms
for salmonellosis, 20t of liver fluke, 144t
for strep throat, 266t of lung fluke, 146t
Cercariae Chronic trachoma, 180t
liver fluke, 144t Cigar body, in sporotrichosis, 150t
lung fluke, 146t Ciprofloxacin
Schistosoma, 142t for anthrax, 300t
Cerebral aspergillosis, 164t, 165f for brucellosis, 304t
Cervical lymphadenopathy, in strep throat, 266t for cat scratch fever, 308t
Cervicitis for chancroid, 190t
chlamydia causing, 178t for donovanosis, 192t
gonorrhea causing, 170t for enterotoxigenic Escherichia coli, 28t
Cestode infection, 132t for plague, 240t
Chagas disease, 287–289, 288t, 289f for tularemia, 94t
Chancroid, 190–191, 190t, 191f for typhoid fever, 306t
Chapare hemorrhagic fever, 254t Cirrhosis
Chapare virus, 254t hepatitis B and, 4t
CHEAP TORCHES mnemonic, in congenital and perinatal hepatitis C and, 8t
infections, 64–66t Clarithromycin, for pertussis, 68t
352 INDEX
Enzyme immunoassay (EIA) antigen detection studies Fidaxomicin, for Clostridium difficile infection, 32t
in blastomycosis, 156t Fifth disease. See Erythema infectiosum (EI)
in histoplasmosis, 158t Filariasis, 106–109, 106t, 107f, 108f
Enzyme immunoassay (EIA) testing Filariform larvae, in threadworm, 126t
in bronchiolitis, 72t Fingernail loss, in hand, foot, and mouth disease, 70t
in cryptosporidiosis, 46t Fitz-Hugh-Curtis syndrome, 170t
in diphtheria, 260t Five-day fever. See Trench fever
in T. pallidum, 176t Flea-borne typhus. See Endemic typhus
Enzyme immunosorbent assay, for Colorado tick fever, 98t “Floppy baby syndrome,” 302t
Enzyme-linked immunosorbent assay (ELISA) Flu. See Influenza
antibody detection by, for Crimean-Congo hemorrhagic fever, 96t Flu-like illness, in Q fever, 318t
antigen-capture, for Crimean-Congo hemorrhagic fever, 96t Fluconazole
in Ebola, 270t for thrush, 264t
in rotavirus, 40t for vulvovaginitis, 194t
in trichinosis, 120t Fluid resuscitation, for cholera, 22t
with Western blot, for Colorado tick fever, 98t Fluorescent treponemal antibody absorption (FTA-ABS), for syphilis, 176t
Eosinophilia, in dwarf tapeworm, 138t Fluoroquinolones
Epidemic hemorrhagic fever. See Hemorrhagic fever with renal syndrome for salmonellosis, 20t
Epidemic parotitis. See Mumps for typhoid fever, 306t
Epidemic typhus, 250–251, 250t, 251f Food, contaminated
body lice and, 292t enterohemorrhagic Escherichia coli from, 26t
Epiglottitis, in croup, 76t hepatitis A due to, 2t
Epstein-Barr virus (EBV), causing mononucleosis, 282t shigellosis from, 18t
Erythema, in Kawasaki disease, 74t yersiniosis from, 30t
Erythema infectiosum (EI), 58–59, 58t, 59f Foodborne botulism, 302t
Erythema migrans (EM), 86t Forchheimer spots, in rubella, 56t
Erythematous candidiasis, 264t Francisella tularensis, 80–81t, 94t
Erythromycin Fungal cultures
for bacillary angiomatosis or peliosis hepatitis in AIDS, 246t in blastomycosis, 156t
for campylobacteriosis, 24t in histoplasmosis, 158t
for chancroid, 190t Fungus ball, 164t, 165f
for chlamydia, 178t Fusobacterium, causing peritonsillar abscess, 258t
for diphtheria, 260t
for donovanosis, 192t
for lymphogranuloma venereum, 198t G
for pertussis, 68t Gardnerella vaginalis, 194t
for psittacosis, 208t Gastroenteritis
for strep throat, 266t in listeriosis, 316t
Eschars, in scrub typhus, 248t from Norovirus, 38t
Escherichia coli in vibriosis, 34t
enterohemorrhagic, 26–27, 26t, 27f viral, from rotavirus, 40t
enterotoxigenic, 28–29, 28t, 29f Gastrointestinal anthrax, 300t
reactive arthritis due to, 182t Gastrointestinal (GI) illnesses, from Giardia, 44t
Esophageal candidiasis, 264t Gastrointestinal mucormycosis, 166t
HIV/AIDS and, 274–277t Gastrointestinal (GI) symptoms, of threadworm, 126t
Ethambutol, for tuberculosis, 204t Generalized tetanus, 314t
Exanthem subitum, 60–61, 60t, 61f Genital warts. See Condylomata acuminata
Extraintestinal disease, from amebiasis, 48t Genitourinary infections, in melioidosis, 320t
Gentamicin
for brucellosis, 304t
F for endocarditis, 246t
Facial rash, “slapped cheek,” in erythema infectiosum, 58t for infective endocarditis, 312t
Famciclovir, for herpes simplex, 184t for plague, 240t
Fatal familial insomnia, 296t for trench fever, 246t
Fatigue for tularemia, 94t
hepatitis C and, 8t German measles. See Rubella
mononucleosis and, 282t Gerstmann-Straussler-Scheinker disease, 296t
Febrile seizures, in exanthem subitum, 60t Giardia lamblia, 44t
Fecal-oral transmission Giardiasis, 43–45, 44t, 45f
cholera from, 22t Giemsa-stained peripheral blood smear examination,
enterohemorrhagic Escherichia coli from, 26t of babesiosis, 92t
hepatitis E from, 12t Gilchrist’s disease. See Blastomycosis
shigellosis from, 18t Glandular fever. See also Mononucleosis
yersiniosis from, 30t tularemia and, 94t
INDEX 355
Peritonsillar abscess (PTA), 257–259, 258t, 259f Polymerase chain reaction (PCR) testing (Continued)
Periungual desquamation, in Kawasaki disease, 74t for severe acute respiratory syndrome, 214t
Permethrin for shigellosis detection, 18t
for head lice, 292t for smallpox, 280t
for pubic lice, 174t, 175f for trench fever, 246t
for scabies, 188t Pontiac fever, Legionnaires’ disease and, 206t
Person-to-person transmission, shigellosis from, 18t Pork tapeworm, 129–131, 130t, 131f
Pertussis, 68–69, 68t, 69f Post-polio syndrome, 284t
Pharyngeal erythema, in strep throat, 266t Poultry
Pharyngitis, in mononucleosis, 282t campylobacteriosis from, 24t
Phthiriasis pubis. See Pubic lice salmonellosis from, 20t
Phthirus pubis, 174t, 175f PPD screening tests, for tuberculosis, 204t
Pinworms, 112–115, 112t, 113f Pregnancy
Pityriasis versicolor. See Tinea versicolor chickenpox during, 62t
Plague, 240–241, 241f dwarf tapeworm in, 138t
bubonic, 240t hepatitis E infection during, 12t
pneumonic, 240t listeriosis during, 64–66t, 316t
septicemic, 240t Lyme disease during, 64–66t
Plasmodium spp., malaria from, 224–225t rubella during, 56t
life cycle of, 224–225t syphilis during, 64–66t
Platelet transfusion, for Crimean-Congo hemorrhagic fever, 96t toxoplasmosis during, 64–66t
Plerocercoids, 132t Zika infection during, 64–66t, 218t
Plumber’s itch. See Cutaneous larva migrans (CLM) Prevotella, causing peritonsillar abscess, 258t
Pneumocystis jirovecii, 274–277t Primaquine, for malaria, 224–225t
Pneumocystis pneumonia, 274–277t Primary amoebic meningoencephalitis (PAM).
Pneumonia See Naegleriasis
in avian influenza, 210t Prion disease, 296–298, 296t, 297f
in melioidosis, 320t Procercoids, 132t
in Q fever, 318t Proctitis, chlamydia causing, 178t
Pneumonic fever, tularemia and, 94t Proctocolitis, in lymphogranuloma venereum, 198t
Pneumonic plague, 240t Proper water filtration, of dracunculiasis prevention, 122t
Podophyllotoxin Prostration
for condylomata acuminata, 172t in Haverhill fever, 244t
for molluscum contagiosum, 196t in smallpox, 280t
Polio, 284–286, 284t, 285f Protoscolices, tapeworms and, 130t
Poliomyelitis. See Polio Pruritus, in scabies, 188t
Poliovirus, 284t Pruritus ani, 112t
Polyarthritis, post-chikungunya, 232t Pseudoappendicitis
Polymerase chain reaction (PCR) testing campylobacteriosis and, 24t
for amebiasis, 48t yersiniosis and, 30t
for anaplasmosis, 90t Pseudoglanders. See Melioidosis
for anthrax, 300t Pseudomembranous colitis. See Clostridium difficile infection
for babesiosis, 92t Pseudomembranous oropharyngeal candidiasis, 264t
for bronchiolitis, 72t Psittacosis, 208–209, 208t, 209f
for brucellosis, 304t Pubic lice, 174–175, 174t, 175f
for chickenpox, 62t Pulmonary mucormycosis, 166t, 167f
for cryptosporidiosis, 46t Pulmonary perspective, of blastomycosis, 156t
for diphtheria, 260t Pulmonary sporotrichosis, 150t
for Ebola, 270t Pulmonary symptoms, of threadworm, 126t
for ehrlichiosis, 88t Puumala virus (PUUV), 236t
for epidemic typhus, 250t Pyrantel pamoate
for hepatitis E detection, 12t for hookworm, 116t
for herpes simplex, 184t for pinworms, 112t
for measles, 52t Pyrazinamide, for tuberculosis, 204t
for MERS, 202t
for mononucleosis, 282t
for mumps, 54t Q
for Norovirus, 38t Q fever, 318–319, 318t, 319f
for pertussis, 68t Quantitative real-time polymerase chain reaction assay, for
for polio, 284t Colorado tick fever, 98t
for rabies, 272t Quinine, for babesiosis, 92t
for Rocky Mountain spotted fever, 84t Quinolone, for vibriosis, 34t
for rubella, 56t Quinsy. See Peritonsillar abscess
for scrub typhus, 248t Quintan fever. See Trench fever
INDEX 361