Neonatal Surgical Emergencies
Neonatal Surgical Emergencies
Neonatal Surgical Emergencies
General Surgery
Prof. Kais Al-Wattar
Part 1
We classify them either according to the relation of the obstructive cause to the wall of the intestine A
physical blockage causing impedance to the passage of the bowel contents results in mechanical obstruction. These causes
are usually divided into those that compress the bowel from outside (extrinsic), those that arise from the wall of the bowel
and obstruct the lumen (intrinsic), and those that arise within the lumen., or to the level of the obstruction in
relation to the mid portion of the jejunum.
General Symptoms: in neonates in the first few weeks of life
-Bilious Vomiting
-Abdominal Distension
-Failure to pass meconium
Radwan showed us the stereotypes of medical students, which was pretty funny, what about medical professors? :P hope
u like it 3:)
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Table 1
Mechanical
Extrinsic
-Malrotation
-Volvulus Neonatorum
-Duplication
-Diaphragmatic Hernia
- Intussusceptions
Intrinsic
-Atresia
-Stenosis
Intraluminal
-Meconium Ileus
-Meconium Plug
Neurogenic
-Hirschsprungs Disease
-Intestinal Neuronal Dysplasia
-Dismosis
Other classifications of intestinal obstruction in neonates are according to the anatomical location of the
obstruction in relation to the mid portion of the jejunum, If the obstruction is higher proximal to the mid
portion of the jejunum its called high anatomical obstruction, when its distal to the mid jejunum we call it low
anatomical obstruction. The causes are summarized in table 2
Table 2
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development, so that a ring of pancreatic tissue surrounds the second or third part of the duodenum. It is most
often seen in association with congenital duodenal stenosis or atresia and is therefore more prevalent in children
with Downs syndrome. Duodenal obstruction typically causes vomiting in the neonate.
*Internal hernia, Internal herniation occurs when a portion of the small intestine becomes entrapped in one
of the retroperitoneal fossae or in a congenital mesenteric defect. The following are potential sites of internal
herniation:
the foramen of Winslow;
a hole in the mesentery;
a hole in the transverse mesocolon;
defects in the broad ligament;
congenital or acquired diaphragmatic hernia;
duodenal retroperitoneal fossae left paraduodenal and right duodenojejunal;
caecal/appendiceal retroperitoneal fossae superior, inferior and retrocaecal;
intersigmoid fossa.
Internal herniation in the absence of adhesions is uncommon and a preoperative diagnosis is unusual.
*Meconium ileus: cystic fibrosis is almost always the underlying cause of this condition, meconium is
normally kept fluid by the action of pancreatic enzymes. In meconium ileus the terminal ileum becomes filled
with thick viscid meconium, resulting in progressive intestinal obstruction.
A sterile meconium peritonitis may have occurred in utero.
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1.4 INVESTIGATIONS
Usually there is disturbance of fluid, electrolytes and acid base balance
Radiological examination:
-All neonates with suspected intestinal obstruction should have plain abdominal X-Ray in supine and erect or
lateral decubitus position, to see the shape of the gas in the intestine and the presence of fluid levels.
Lateral decubitus position
When medical professionals use this term to describe the position of a patient, they first state the part of the body on
which the patient is resting followed by the word "decubitus". For example, the right lateral decubitus would mean that the
patient is lying on his or her right side. Another example is angina decubitus, (chest pain while lying down)
In radiology, this term implies that the patient is lying down with the X-ray being taken parallel to the horizon.
Patient in lateral decubitus position
-All must have antero-posterior and left side down decubitus X-Rays.
-Radiology is usually difficult to differentiate dilated small bowel from collapsed large bowel before the first
year of age.
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Malrotation
In cases of Malrotation, the upper GIT contrast study is
characteristic; it usually shows failure of the duodeno-jejunal
junction to cross to the left of the spine, obstruction of the
duodenum and abnormal right-sided jejunum.
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Corkscre
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Target sign
Longitudinal U.S.
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SUMMARY
A. Intestinal Atresia, seriously guys no need to draw a table!
The commonest cause of neonatal intestinal obstruction.
Caused by: just theories
-Failure of recanalization of the intestine during the development of the GIT.
- Segmental occlusion of blood supply in the intrauterine life, leads to failure of development of that
segment and atresia.
-No clear cause.
Table 3
B. Duodenal Obstruction
Causes:
-Duodenal atresia (the most
common)
-Duodenal duplication
-Annular Pancreas
-Ladds band
-Duodenal Hematoma
(usually following blunt abdominal
trauma)
Diagnosed by:
-Maternal Polyhydromnios
-Bilious vomiting
-Upper abdominal distension
-Associated other anomalies;
congenital heart disease, skeletal
abnormalities and down syndrome
-Later signs of fluid and electrolytes
imbalance and sepsis
-Radiology, double bubble shadow
mostly with duodenal atresia
Treatment:
-Nasogastric suction
-Intravenous fluid
-Correction of electrolytes and acidbase balance
-Treat sepsis
-Surgery (dealing with the
underlying cause)
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Type 1
The bowel is continuous, but the
lumen is occluded by a
membrane.
Type2
The lobes of small intestine are
connected by a band, the
proximal lobe is dilated and the
distal lobe is collapsed, and there
is a mesentery between them.
Type 3
When there is no mesentery,
there is a missing segment
between the proximal dilated
lobe and the distal collapsed lobe.
Type 4
Multiple areas of intestinal
atresia of different types,
sometimes called Christmas Tree
type of atresia.
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2.2 MALROTATION
A. Embryology
Usually there is arrest of the rotation of the cecocolic loop at 180 degrees and the
caecum lie in the hypochondrium in front of and adjacent to the duodenum, there is a
narrow base of the mesentery of the entire gut attached to posterior abdominal wall
along the axis of the superior mesenteric artery.
Ladds band from the cecocolic loop crosses and compresses the second part of the
duodenum causing intermittent obstruction.
B. Clinically
The patient might be asymptomatic and then develop the symptoms when he is older,
family history of a similar condition might be encountered and the child might have other
associated congenital anomalies.
The presenting symptoms might be in the form of:
-Duodenal obstruction.
-Intermittent intestinal obstruction, when the segment rotate intermittently such additions
makes the difference between copy-pasting slides and actual tafree3 3:P.
-As a complication of the condition (Volvulus).
The radiological features which indicate the diagnosis in the uncomplicated case are:
-Plane x-ray showing gasless abdomen.
-Barium meal shows the dilatation of the stomach and the DJ flex :P is normally to the left of the
spine but now its to the right of the spine, which is another feature of Malrotation, the small
bowel is on the right side and the large bowel is on the right side, classical finding 8).
-Barium enema shows arrest at the mid site of the colon.
C. Treatment
-Pre Operative.
-Surgery.
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Part 3
Cystic duplication
Tubular duplication
B. Presentation
-Asymptomatic
-Abdominal mass
-Complications, intestinal obstruction, bleeding, perforationetc.
Duplication of the Jejunum usually present as cyst located at the mesenteric
side stretched by the normal jejunum, or may present as tubular duplication
which sometimes communicated with the adjacent intestine.
Large bowel duplication is usually tubular and maybe communicating.
C. Treatment
The treatment of duplication cyst is excision of the whole lesion, usually with the
related normal bowel segment because they have the same blood supply.
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THATS ENOUGH!
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3122
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