From The Archives of The AFIP: Endometriosis: Radiologic-Pathologic Correlation
From The Archives of The AFIP: Endometriosis: Radiologic-Pathologic Correlation
From The Archives of The AFIP: Endometriosis: Radiologic-Pathologic Correlation
CME FEATURE
Paula J. Woodward, MD • Roya Sohaey, MD • Thomas P. Mezzetti, Jr,
See accompanying
LCDR, USNR, MC
test at http://
www.rsna.org
/education Endometriosis is an important gynecologic disorder primarily affecting
/rg_cme.html
women during their reproductive years. Pathologically, it is the result
of functional endometrium located outside the uterus. It may vary
LEARNING
OBJECTIVES
from microscopic endometriotic implants to large cysts (endometrio-
FOR TEST 5 mas). The physical manifestations are protean, with some patients be-
After reading this ing asymptomatic and others having disabling pelvic pain, infertility, or
article and taking
the test, the reader
adnexal masses. Symptoms do not necessarily correlate with the sever-
will be able to: ity of the disease. Ultrasonographic (US) features are variable and can
■ Outline the pro- mimic those of other benign and malignant ovarian lesions. Low-level
posed mechanisms internal echoes and echogenic wall foci are more specific US features
of pathogenesis of
endometriosis and for endometriomas. Magnetic resonance imaging improves diagnostic
how they relate to accuracy, with endometriotic cysts typically appearing with high signal
the distribution of
disease. intensity on T1-weighted images and demonstrating “shading” on T2-
■ Identify which im- weighted images. The ovaries are the most common sites affected, but
aging features are endometriosis can also involve the gastrointestinal tract, urinary tract,
more specific for en-
dometriosis and help chest, and soft tissues. Small implants and adhesions are not well eval-
to distinguish it from uated radiologically; therefore, laparoscopy remains the standard of ref-
other adnexal masses.
■ Describe the un-
erence for diagnosis and staging. Both medical and surgical treatment
usual manifestations options are available depending on the patient’s specific case.
and complications
that can be seen with
endometriosis.
Bldg 54, Room M-121, Washington, DC 20306-6000; the Department of Radiology, Oregon Health Sciences University, Portland (R.S.); and
the Department of Radiology, University of Utah, Salt Lake City (P.J.W.). Received July 7, 2000; revision requested July 24; revision received
August 1; accepted August 3. Address correspondence to P.J.W. (e-mail: woodwardp@afip.osd.mil).
The opinions and assertions contained herein are the private views of the authors and are not to be construed as official nor as representing the
views of the Departments of the Navy or Defense.
©RSNA, 2001
194 January-February 2001 RG ■ Volume 21 • Number 1
Introduction Epidemiology
Endometriosis is classically defined as the pres- Endometriosis is found predominantly in women
ence of functional endometrial glands and stroma of childbearing age. The mean age at diagnosis is
outside the uterine cavity (ectopic as opposed to 25–29 years, but it is often greater in women who
normally located or eutopic endometrium). In present with infertility rather than pelvic pain (1).
older literature, endometriosis was further classi- Endometriosis is not uncommon among adoles-
fied as endometriosis interna and endometriosis cents. Approximately half of women under 20
externa. Endometriosis interna referred to en- years of age who have chronic pelvic pain or dys-
dometrial tissue within the uterine musculature, pareunia have the disease (2,3). Obstructive
and endometriosis externa referred to endome- müllerian duct anomalies of the cervix or vagina
trial tissue in all other sites. Currently, the term account for most cases of endometriosis in girls
adenomyosis has replaced endometriosis interna. under the age of 17 years (4). About 5% of endo-
Adenomyosis is considered a distinct and differ- metriosis cases are seen in postmenopausal
ent clinical entity because its pathogenesis, symp- women, and exogenous estrogen replacement
toms, and epidemiology differ from those of en- therapy is suggested to play a role (5). In rare
dometriosis. Endometriosis externa is now simply cases, men undergoing long-term estrogen thera-
called endometriosis and is the condition reviewed py may be affected (5).
in this article. The prevalence of endometriosis is difficult to
Endometriosis is a common and important determine accurately. Laparoscopy or surgery is
clinical problem of women, predominantly those required for the definitive diagnosis. Endometri-
in the reproductive age group. At pathologic osis has been reported in 4.1% of asymptomatic
analysis, it can vary from microscopic foci to large, women undergoing laparoscopy for tubal ligation.
grossly visible endometriotic cysts (endometrio- However, in the same study, 20% of women un-
mas). Radiologists are often involved in the diag- dergoing laparoscopic investigation for infertility
nosis and work-up of this disease in one of two and 24% of women with pelvic pain had endo-
scenarios: They are asked to exclude endometri- metriosis (6). Overall prevalence, including both
osis in a woman with pelvic pain or infertility or symptomatic and asymptomatic women, is esti-
they are considering endometriosis in the differ- mated to be 5%–10% (7,8).
ential diagnosis of an adnexal mass. When social and economic factors are accounted
Radiologists often use the terms endometriosis for, the prevalence of endometriosis is the same in
and endometriomas interchangeably. It is important women of different races (9,10). In a recent study,
to remember, however, that endometriomas are investigators compared menstrual characteristics
only a part of the disease process, which also in- that would increase peritoneal exposure to men-
cludes endometriotic implants and adhesions. All of strual fluid with the risk of developing endometri-
these features are important in the staging of endo- osis. The three characteristics studied were age of
metriosis, and normal results from an imaging pro- menarche, duration of menstrual flow, and men-
cedure do not rule out the presence of disease. strual cycle length. The only menstrual characteris-
To help radiologists better understand this tic that was significantly associated with endometri-
disease process, we review its epidemiology, osis was a menstrual cycle length of less than 28
pathogenesis, staging, and clinical features. Al- days (11). An increased prevalence of endometri-
though its imaging characteristics overlap with osis in families has been observed, and therefore a
those of other adnexal masses, those features genetic effect has been suggested (12).
more specific to endometriosis are discussed,
along with the strengths and weaknesses of the Pathogenesis
various imaging modalities. Endometriosis can Endometriosis is a complex disorder, and its
also occur in nongynecologic sites. A knowledge causes are probably multifactorial. Three theories
of these locations, their clinical manifestations, of histogenesis have been proposed: (a) metastat-
and radiologic appearances will aid radiologists in ic theory (retrograde menstrual implantation,
considering endometriosis in the differential diag- vascular and lymphatic spread, and intraopera-
nosis. Atypical manifestations of endometriosis, tive implantation), (b) metaplastic theory, and
complications, and treatment are also discussed. (c) induction theory (Fig 1). In addition, re-
searchers are presently investigating the role of
growth factors, immunity, and other mechanisms
RG ■ Volume 21 • Number 1 Woodward et al 195
1. 2.
Figures 1, 2. (1) Drawing depicts the potential mechanisms of endometriosis pathogenesis, including retrograde
menstruation (a), lymphatic spread (b), hematogenous spread (c), and coelomic metaplasia (d). Induction of undif-
ferentiated mesenchyma by unidentified endometrial substances is also theorized. (2) Drawing illustrates common
sites of endometriosis.
that may contribute to the development of this A second theory of histogenesis is that of meta-
disorder. plastic differentiation of serosal surfaces (coelomic
The most widely accepted theory is that endo- epithelium) or müllerian remnant tissue. Both
metriosis results from metastatic implantation endometrial and peritoneal cells derive from the
from retrograde menstruation (7,13,14). The coelomic wall–epithelium. The theory suggests
theory assumes transportation of endometrial tis- the possibility of peritoneal cells differentiating
sue from the uterus in a retrograde fashion into into functioning endometrial cells. The strongest
the peritoneal cavity. The endometrial cells re- evidence for this theory is the demonstration of
main viable and implant on serosal surfaces out- endometriosis in women lacking functional
side the uterus. The occurrence of retrograde eutopic endometrium (eg, those with Turner
menstruation has been documented with diag- syndrome, gonadal dysgenesis, uterine agenesis)
nostic laparoscopy and studies of peritoneal di- and in men (22). In the rare cases of endometri-
alysis fluid. Up to 90% of women have bloody osis occurring in men, they have usually received
peritoneal fluid during the perimenstrual period high doses of estrogen, which is sometimes done
(15–17). Investigators have shown the in vitro in the treatment of prostate carcinoma (7,23,24).
growth potential of shed endometrium and have In these men, the cause is possibly hyperplasia
demonstrated viable endometrial cells in perito- and spread of endometrial tissue from the pros-
neal fluid (7,18,19). Further evidence for this tatic utricle (a müllerian remnant) (7).
theory is suggested by the anatomic pattern of A third theory, the induction theory of endo-
the disease within the dependent areas of the pel- metriosis, is a combination of the first two. It
vis (Fig 2) (20). Endometriosis is also seen with suggests that shed endometrium releases sub-
greater frequency in women with excessive retro- stances that induce undifferentiated mesenchyma
grade flow due to obstructive anomalies of mül- to form endometriotic tissue (7). These sub-
lerian duct development (21). Other possible stances have not been identified, but animal re-
routes of metastatic spread include transport of search has shown the formation of endometrial
endometrial cells to distant sites via the blood glands (but not stroma) when experiments have
stream or lymphatic channels or iatrogenically been performed to test this theory (7,25).
during surgery or needle biopsy (22).
196 January-February 2001 RG ■ Volume 21 • Number 1
Table 1
Regardless of which theory is correct, other Most Common Sites for Endometriotic Im-
factors probably play a role in the occurrence of plants and Adhesions
endometriosis, since all women are not equally
Implants Adhesions
susceptible. Impairment of the immune response
Location (%) (%)
to remove peritoneal menstrual debris has been
suggested as an additional factor. Women with Ovaries 76 39
endometriosis have been found to have abnor- Anterior and
malities of T-cell–mediated cytotoxicity, natural posterior cul-de-sac 69 13
killer cell activity, B-cell function, and comple- Posterior broad ligament 47 43
Uterosacral ligament 36 7
ment deposition (26,27). The role of growth fac-
Uterus 11 3
tors and factors critical to cell implantation are
Fallopian tubes 6 26
also receiving attention (7). Sigmoid colon 4 12
Finally, the biologic behavior of ectopic en- Ureter 3 2
dometrial glands is variable and adds to the com- Small intestine 0.5 3
plexity of the disease. Ectopic endometriotic im-
plants generally respond to circulating hormones Source.—Adapted from reference 20.
in the same manner as eutopic endometrium
(though to a lesser degree). Estrogen stimulates
glandular growth, whereas progesterone inhibits
it. However, ectopic endometrium often behaves patches (usually less than 2 cm). The amount of
unpredictably, which leads to difficulties in diag- pigment in the implant appears to increase with
nosis and treatment (22). the age of the lesion. They may initially be un-
pigmented or appear as white, yellow, or red fo-
Pathologic Features ci, which progress to a more mature-appearing
Gross pathologic findings of endometriosis de- blue or brown lesion (Figs 3, 4) (22,28). These
pend on the duration of the disease and depth of brown, ecchymotic areas have been described as
penetration of the lesions. Endometriotic im- “powder burns.” Implants may change in appear-
plants vary from punctate foci to small stellate ance during the menstrual cycle, becoming more
swollen and congested during menses and bleed-
ing in some cases. These mature endometriotic
foci initiate an inflammatory response, with areas
RG ■ Volume 21 • Number 1 Woodward et al 197
a. b.
Figure 5. Left ovarian endometrioma in a 30-year-old woman. (a) Transabdominal US scan shows a hypoechoic
mass replacing the left ovary (arrows). Note the thickened wall. (b) Photograph of the gross specimen (external sur-
face on the left and internal surface on the right) reveals stellate patches of hemorrhage on the external surface (solid
arrows) and a thick-walled, dark, irregular internal cyst lining. A portion of the fallopian tube was adherent to the
endometrioma (open arrow). Scale is in centimeters.
a. b.
Figure 6. Right ovarian endometrioma in a 25-year-old woman. (a) Transvaginal US scan shows an echogenic
ovarian cyst filled with low-level echoes. (b) Photograph of the resected cyst, which has been opened, shows dark-
brown, viscous blood products. This appearance has been called a chocolate cyst. Multiple irregular hemorrhagic
foci are seen on the external surface of the cyst.
of organizing hemorrhage, fibrosis, and adhesion sue. Cyst walls are generally thick and fibrotic and
formation. Extensive adhesions can distort the commonly have areas of discoloration and dense
normal pelvic anatomy and obliterate the pouch fibrous adhesions. The cyst lining can vary from
of Douglas (22,28–30). The most common site smooth and pale to shaggy and brown (Fig 5).
of involvement is the ovary, but virtually all pel- Although cyst contents can be watery, they more
vic organs can be affected by the disease (Table typically are composed of thick, dark, degener-
1) (20). ated blood products. This appearance has been
Endometriotic cysts (endometriomas) gener- called “chocolate cyst” (Fig 6). Endometriomas
ally occur within the ovaries and are the result of
repeated cyclic hemorrhage within a deep implant.
They may completely replace normal ovarian tis-
198 January-February 2001 RG ■ Volume 21 • Number 1
a. b.
Figure 7. Microscopic appearance of an endometriotic implant. (a) Medium-power photomicrograph (original
magnification, ´4; hematoxylin-eosin stain) shows endometriotic glands and stroma (center). The endometriotic tissue
is surrounded by fibrosis (arrows) as well as degraded blood products and inflammatory debris (*). (b) High-power
photomicrograph (original magnification, ´80; hematoxylin-eosin stain) shows dark-brown particles of hemosiderin
or hemofuscin (straight arrows) and scattered red blood cells (curved arrows). A layer of endometriotic glands is
partially visible in the lower left corner.
are bilateral in up to half of the cases and may be (22,30). In rare cases, endometriosis may lack
large, although they seldom exceed 15 cm in di- glands (stromal endometriosis) (22).
ameter (22,29). Large lesions and lesions with
wall nodularity should be carefully sampled to Clinical Characteristics
rule out malignancy. Symptoms associated with endometriosis include
At microscopic analysis, endometriosis is com- infertility and pelvic pain. These nonspecific
posed of endometrial glands, stroma, and occa- symptoms can accompany a wide variety of disor-
sionally smooth muscle fibers. As with eutopic ders and are not pathognomonic for endometri-
endometrium, the ectopic endometrial foci re- osis. Unusual symptoms linked to atypical loca-
spond to circulating hormones and may show tion of disease can also occur. The extent of en-
secretory changes during the second half of the dometriosis does not always correlate with the
menstrual cycle and stromal decidualization dur- severity of symptoms, which further complicates
ing pregnancy (28). Hemorrhage within these the diagnosis. However, endometriosis should be
foci results in an inflammatory response, with in- considered in any woman of reproductive age with
filtration of histiocytes that become pigment pelvic pain or infertility.
laden with hemosiderin and hemofuscin (Fig 7) Infertility, with or without pelvic pain, may be
the presenting complaint in women with endo-
metriosis. It is estimated that 30%–50% of women
RG ■ Volume 21 • Number 1 Woodward et al 199
with endometriosis are infertile, and 20% of in- ment. Pelvic organs may be fixed from adhesions,
fertile women have endometriosis (6,31). Al- with the uterus often fixed in a retroverted posi-
though the association between the two is well tion (7). The physical examination should be
established, the causal mechanism is debated. An performed during early menses because implants
acceptable explanation is that endometriomas are more likely to be large and tender at this time
and adhesions cause pelvic distortion, which in the cycle. However, most women with endo-
leads to impaired ability of the fallopian tubes to metriosis have normal or nonspecific results from
capture ovum (7,31). In cases in which minimal physical examinations, and laparoscopy is neces-
endometriosis is present, the clinician must de- sary for the definitive diagnosis (13).
cide if the finding is incidental. Some proposed Laparoscopy is the standard of reference in the
mechanisms for infertility in women with mini- diagnosis of endometriosis. Although histologic
mal disease include abnormalities related to au- analysis of biopsy specimens to confirm the diag-
toimmunity and peritoneal fluid factors (31). nosis is desirable, it is not necessary. Staging of
Pelvic pain is a frequent complaint from the disease can also be done during laparoscopy.
women with endometriosis. Common symptoms Endometriotic implants, endometriomas, and ad-
include dysmenorrhea, dyspareunia, chronic pel- hesions are the typical findings. Implants may
vic pain, back pain, and rectal discomfort (8). measure from a few millimeters to a few centime-
The pain is not always cyclic, and endometriosis ters and may be superficial or deep. Because
is present in approximately one-third of patients endometriotic implants can vary in appearance,
with chronic pelvic pain (31). the accuracy of diagnosis depends on the ability
Unusual symptoms may occur when endome- of the surgeon to recognize the disease (Figs 3,
triotic implants occur in atypical locations. In- 4) (8). A pattern of lesion maturity has also been
volvement of the gastrointestinal tract may mani- described, with subtle findings seen in young
fest with catamenial diarrhea, rectal bleeding, women and more characteristic features identi-
and constipation. Bladder involvement may re- fied in the same women a decade later (35).
sult in urgency, frequent urination, and hema- Endometriotic cysts may be seen, most com-
turia. Ureteral involvement may cause urinary monly involving the ovaries. Inflammatory re-
obstruction and flank pain. Pleuritic chest pain, sponse to active endometrial lesions can lead to
pneumothorax, pleural effusions, or cyclic he- fibrosis and adhesions. Severe adhesions may ac-
moptysis can occur with pulmonary involvement tually compartmentalize the pelvis and impede
(32). Cyclic headaches, seizures, and subarach- laparoscopic evaluation.
noid hemorrhage have been described with brain The most widely used staging system for en-
lesions (33,34). Cutaneous lesions may manifest dometriosis is the 1985 Revised Classification of
with catamenial bleeding and tenderness (31). Endometriosis published by the American Fertil-
ity Society (8,36). This system consists of three
components: evaluation of the endometrial im-
Diagnostic Evalu-
plants (location, size, and depth of penetration),
ation: Physical Examina- degree of cul-de-sac obliteration, and evaluation
tion, Laparoscopy, and Staging of adhesions (amount of surface area involvement
Physical findings for endometriosis are nonspe- and appearance) (Table 2). On the basis of their
cific. Localized tenderness along the uterosacral score, patients are categorized as having mini-
ligaments and the cul-de-sac is often present. mal, mild, moderate, or severe disease. Critics of
Thickened or nodular ligamental or rectovaginal staging note that the stage of disease does not
masses may be palpated. Adnexal tenderness or
masses may be found if there is ovarian involve-
200 January-February 2001 RG ■ Volume 21 • Number 1
Table 2
Endometriosis Staging System of the American Fertility Society
A. Endometrial Implants
Size
Location Depth of Penetration <1 cm 1–3 cm >3 cm
Peritoneum Superficial 1 2 4
Deep 2 4 6
Ovary Right superficial 1 2 4
Right deep 4 16 20
Left superficial 1 2 4
Left deep 4 16 20
B. Obliteration of the Posterior Cul-de-sac
Degree of Obliteration Score
Partial 4
Complete 40
C. Adhesions
Amount of Surface Involvement
< 1/3 1/3–2/3 > 2/3
Location Appearance Enclosure Enclosure Enclosure
Ovary Right filmy 1 2 4
Right dense 4 8 16
Left filmy 1 2 4
Left dense 4 8 16
Fallopian tube Right filmy 1 2 4
Right dense 4 8 16
Left filmy 1 2 4
Left dense 4 8 16
Note.—Stage I (minimal) = score 1-5, stage II (mild) = score 6-15, stage III (moderate) = score 16-40, stage
IV (severe) = score >40. From reference 36.
Radiologic
necessarily correlate with the severity of symp-
toms (7,13), and consistent treatment options
Evaluation of Endometriosis
based on stage of disease have not been estab- Not unexpectedly, radiologic evaluation of small
lished (7). Despite these limitations, staging is endometriotic implants is limited; therefore, the
thought to offer some standardization in stratify- radiologist’s role is generally to identify and eval-
ing disease severity and in assessing response to uate endometriotic cysts. Because symptoms are
therapy. variable, patients may be referred for a diverse ar-
ray of imaging studies, including excretory urog-
raphy, barium studies, and computed tomogra-
phy (CT). These techniques lack both sensitivity
RG ■ Volume 21 • Number 1 Woodward et al 201
a. b.
Figure 8. Diffuse endometriosis in a 27-year-old woman
with pelvic pain. (a) Transabdominal midline sagittal US
scan shows a complex cystic mass (white arrow) posterior
to the uterus (U) filling the cul-de-sac (black arrow, right
ovary). (b) Transvaginal US scan shows that the mass is
contiguous with the serosal surface of the right ovary (ar-
row). (c) Photograph of the resected specimen shows ex-
tensive fibrous tissue and cysts filled with hemorrhage (ar-
rows). This mass obliterated the cul-de-sac and was ad-
herent to both the right ovary and appendix. Scale is in
centimeters.
Ultrasonography
Both transvesicular and transvaginal US should
be performed. Cysts involving the ovaries should
be completely characterized, with attention given
to internal echogenicity, wall morphology, and
effects on surrounding organs. Because the cul-
c. de-sac is commonly involved, care should be
taken during scanning to evaluate this area com-
pletely (Fig 8).
and specificity, and a variety of nonspecific radio- Endometriomas can have a variety of US ap-
logic findings may be seen. Ultrasonography (US) pearances. The majority exhibit diffuse low-level
is the most common imaging modality used to internal echoes, with the “classic” endometrioma
evaluate suspected endometriosis. However, it is being described as a homogeneous, hypoechoic
applicable only to the evaluation of endometriotic focal lesion within the ovary (Figs 5, 6) (37–41).
cysts; detection of adhesions or implants with US In one recent study of 40 endometrial cysts, 95%
is only anecdotal. Magnetic resonance (MR) im- demonstrated this finding (37). In rare cases,
aging has proved to be a very useful and more spe- they may be anechoic, mimicking a functional
cific imaging technique and is often used as a ovarian cyst.
problem-solving tool.
202 January-February 2001 RG ■ Volume 21 • Number 1
a. b.
Figure 9. Endometrioma with thin septations in a 26-year-old woman. Sagittal (a) and transverse (b) transvaginal
US images show a cystic mass posterior to the uterus in the cul-de-sac. It is filled with low-level internal echoes and
has a thin septation within it (long arrow). Bright echogenic foci are seen within the cyst wall (short arrows).
a. b.
Figure 10. Endometrioma with thick septations in a 35-year-old woman. (a) Transvaginal US scan shows
thick septations (arrow) with areas of wall irregularity (arrowhead). (b) Photograph of the gross specimen
shows an irregular wall and septations (forceps). This appearance overlaps with that of a neoplasm. Scale is in
centimeters.
12. 13.
Figures 12, 13. (12) Dermoid cyst. Transvaginal US scan demonstrates a cystic mass with an area of low-level
echoes that could be mistaken for an endometrioma. However, the lesion also has a well-defined area of increased
echogenicity (arrow), a finding that makes a dermoid cyst the more likely diagnosis. (13) Hemorrhagic cyst mimick-
ing an endometrioma. Transvaginal US scan shows a hypoechoic cystic lesion in the left ovary. The patient had pre-
sented with acute pain, a symptom that makes the diagnosis of a hemorrhagic cyst more likely. A 6-week follow-up
scan showed resolution.
a. b.
Figure 15. Bilateral endometriomas in a 27-year-old
woman. (a) Axial T1-weighted MR image shows bilat-
eral high-signal-intensity adnexal masses (solid arrows).
An intrauterine device is seen within the uterus (open
arrow). (b) On a T1-weighted fat-suppressed image,
these masses remain bright, a finding that effectively
rules out a diagnosis of dermoid cyst. (c) T2-weighted
image shows shading with mixed high and low signal
intensity in both lesions (arrows). Open arrow = in-
trauterine device.
a. b.
Figure 16. Bilateral endometriomas in a 46-year-old woman. (a) Axial T1-weighted MR image shows a unilocular
high-signal-intensity mass on the right and a multilocular high-signal-intensity mass on the left (arrows). (b) T2-
weighted image shows that the right-sided mass remains high in signal intensity (short arrow), whereas the one on the
left shows shading with marked signal loss (long arrows). The variable appearance of these lesions is thought to re-
flect the concentration of blood products.
fibrous nature of the cyst wall give it a low-sig- images, but the signal is considerably less intense
nal-intensity appearance on both T1- and T2- than that of fat or blood (55). The most prob-
weighted images. lematic lesions to differentiate are hemorrhagic
Looking at both the multiplicity and signal in- corpus luteum cysts, whose MR imaging appear-
tensity of lesions, Togashi et al (42) found that a ance can be similar to that of endometriomas.
“definitive” diagnosis of an endometrioma was Hemorrhagic cysts are usually unilocular as op-
made when a cyst was hyperintense on T1- posed to endometriomas, which are frequently
weighted images and shading was observed on multilocular and bilateral. In addition, hemor-
T2-weighted images. The diagnosis was also “de- rhagic cysts do not exhibit shading on T2-
finitive” when multiple hyperintense cysts were weighted images and will resolve with time (46).
seen on T1-weighted images regardless of their A follow-up examination (this can be done with
signal intensity on T2-weighted images. In their US) can confirm the diagnosis. Ovarian carci-
study, MR imaging yielded an overall sensitivity, noma can occasionally have internal hemorrhage.
specificity, and accuracy of 90%, 98%, and 96%, Visualization of solid components, septations, and
respectively. Because these cysts contain blood a size larger than expected for an endometrioma
products of different ages and concentrations, are features suggestive of malignancy.
cyst appearance can be variable. Those lesions Despite advances in technology, the diagnosis
that are not hyperintense on T1-weighted images of small endometriotic implants remains elusive.
can be difficult to distinguish from other adnexal Their signal intensity is quite variable. They may
masses (42,55). appear similar to normal endometrium (ie, low
Other lesions that appear with high signal in- signal intensity on T1-weighted images and high
tensity on T1-weighted images include dermoids, signal intensity on T2-weighted images), be hy-
mucinous cystic neoplasms, and hemorrhagic pointense with all pulse sequences, or be hyper-
masses. Dermoids can be recognized and differ- intense with all pulse sequences (Fig 17) (43,55,
entiated from endometriomas by the presence of 56). Implants can enhance with gadolinium; how-
chemical shift artifact and signal drop-out on the ever, this characteristic is neither sensitive nor
fat-suppression images. Mucinous lesions can specific (47).
have increased signal intensity on T1-weighted
Complications
Adhesions are an extremely common and impor-
tant complication of endometriosis, and an at-
RG ■ Volume 21 • Number 1 Woodward et al 207
a. b.
Figure 17. Endometriosis with an endometriotic cyst, implants, and adhesions. Axial T1-weighted (a) and
T2-weighted (b) MR images show the ovaries located more posteriorly than normally seen. The left ovary is
replaced by an endometrioma, which has low signal intensity on the T1-weighted image and which shows poste-
rior dependent shading on the T2-weighted image (solid curved arrow). There is a large endometriotic implant
on the surface of the right ovary, which has high signal intensity with both pulse sequences (open straight arrow).
Other implants were present at laparoscopy that were not seen on MR images. Note the adhesion extending
from the right ovary to the posterior pelvic wall (solid straight arrow in b), which is made conspicuous by fluid
on either side. Open curved arrow = uterus.
a. b.
Figure 20. Bilateral endometrioid carcinomas in a 30-year-old woman with pelvic pain and a palpable mass.
(a) Axial CT scan shows bilateral ovarian masses with large, enhancing solid components (arrows). (b) Pho-
tograph of the resected left ovary shows a large solid component, as well as blood within the cystic portion.
Endometriosis and endometrioid carcinoma were found at histologic analysis.
a. b.
Figure 21. Large atypical endometrioma in a 32-year-old woman with right-sided abdominal pain and infertility.
(a) CT image shows a complex right adnexal mass extending into the upper abdomen. Note the irregular nodular
enhancement within the wall of the mass (arrows). (b) Photograph of the gross specimen shows prominent soft-tissue
masses in the wall of the cyst. The findings are suggestive of malignancy, and the solid areas must carefully sampled.
Scale is in centimeters.
b.
210 January-February 2001 RG ■ Volume 21 • Number 1
b.
Figure 23. Endometriosis at the rectosigmoid junction
in a 28-year-old woman with menorrhagia and pelvic pain
who presented with a 6-week history of rectal bleeding.
(a) Double-contrast barium enema image shows circum-
ferential narrowing of the rectosigmoid colon (arrow).
(b) Photograph of the gross specimen shows marked
thickening of the bowel wall. In this case, the patient’s
clinical presentation, along with location and lack of mu-
cosal irregularity, were suggestive of endometriosis. Se-
vere endometriosis and dense adhesions were found at
surgery.
a.
Genitourinary Tract
Endometriotic implants may affect the urinary
tract in up to 20% of cases, but involvement is
usually asymptomatic except in conjunction with Figure 24. Endometriosis involving the bladder in a
severe pelvic disease (22,63). The bladder is the 42-year-old woman with hematuria and a history of
most frequently involved organ, followed by the pelvic endometriosis. Collimated view of the bladder
ureters. Only scattered cases of renal or urethral from an excretory urographic study shows an irregular
involvement have been reported (22). When the filling defect on the dome of the bladder (arrow). The
bladder is involved, endometriotic implants are appearance is nonspecific and requires biopsy to rule
often confined to the serosal surface but can infil- out malignancy.
trate the muscle and appear as mural masses pro-
jecting into the bladder lumen. These masses are
typically near the dome of the bladder and can be and cystoscopy with biopsy is required for a de-
seen during excretory urography or with US, CT, finitive diagnosis.
or MR imaging (Fig 24). This appearance is gen- The distal ureter is the most common ureteral
erally indistinguishable from that of a neoplasm, segment involved. Endometriotic foci may im-
plant on ureteral adventitia. Direct invasion of
the ureter can lead to hyperplasia and fibrosis of
RG ■ Volume 21 • Number 1 Woodward et al 211
Figure 25. Endometriosis of the distal right ureter in a 44-year-old woman with episodic painful
hematuria. (a) A 10-minute image from an excretory urographic study shows dilatation of the right
collecting system and proximal ureter (arrows). (b) Retrograde ureterogram shows a short, ta-
pered stricture in the distal right ureter (arrow). (c) Photograph of resected portions of the ureter
shows marked wall thickening and luminal narrowing.
a. b.
Chest
Well-documented endometriosis of the chest,
thoracic endometriosis syndrome (TES), is un-
common, and the diagnosis is usually established
on clinical grounds (64). The two theories enter-
tained for the development of TES are micro-
embolization and peritoneal-pleural migration. In
c. the microembolization theory, it is postulated that
endometrial tissue can be transported through the
lymphatic or vascular channels to the lung paren-
the muscularis and lamina propria, resulting in chyma. Alternatively, endometrial tissue may in-
luminal narrowing (22). Ureterography reveals a volve the pleura by migrating from the peritoneal
short or medium length ureteral stricture, usually cavity to the pleural cavity through diaphrag-
near the inferior aspect of the sacroiliac joint. matic defects. Pleural lesions are almost exclu-
The ureter may have a smooth stricture, abrupt sively right-sided, whereas lung lesions have no
tapering, and sharp medial angulation (Fig 25). such predilection (22). Regardless of pathophysi-
This narrowing can cause dilatation and even ology, TES is generally associated with coexistent
complete obstruction of the proximal ureter. pelvic endometriosis and usually occurs 5 years
These findings are nonspecific, and other causes after the diagnosis of pelvic endometriosis (64).
for ureteral stricture are in the differential diag-
nosis.
212 January-February 2001 RG ■ Volume 21 • Number 1
a. b.
Figure 29. Rectus muscle endometrioma in a 35-year-old woman with a history of prior abdominal hysterectomy
but not endometriosis. Transverse (a) and longitudinal (b) US scans of the abdominal wall show a hypoechoic mass
within the right rectus muscle (large arrows). The small arrow in a points to the midline. LL = left rectus muscle,
RR = right rectus muscle.
a. b.
Figure 30. Subcutaneous endometrioma in a 42-year-old woman with a 10-year history of a lump in her right
groin. (a) CT scan shows a soft-tissue-attenuation mass with surrounding inflammatory changes (arrow). (b) Low-
power photomicrograph (original magnification, ´8; hematoxylin-eosin stain) of the implant shows endometriotic
glands and stroma (arrows) scattered in a background of reactive fibrosis.
Medical treatment strategies focus on hor- 3. Chatman DL, Ward AB. Endometriosis in adoles-
monal manipulation of the menstrual cycle to cents. J Reprod Med 1982; 27:156–160.
4. Huffman JW. Endometriosis in young teen-age
create states of pseudopregnancy, pseudomeno- girls. Pediatr Ann 1981; 10:44–49.
pause, or chronic anovulation. Frequently pre- 5. Clement PB. Pathology of endometriosis. Pathol
scribed agents include danocrine (Danazol; Ann 1990; 25:245–295.
Sanofi-Winthrop, New York, NY), gonadotro- 6. Eskanazi B, Warner M. Epidemiology of endome-
pin-releasing hormone agonists (Lupron; TAP triosis. Obstet Gynecol Clin North Am 1997;
24:235–258.
Pharmaceuticals, Deerfield, Ill), oral contracep- 7. Olive DL, Schwartz LB. Endometriosis. N Engl J
tive pills, and other progestational agents. Dano- Med 1993; 328:1759–1769.
crine has been shown to demonstrate a decrease 8. Lu PY, Ory SJ. Endometriosis: current manage-
in disease in 60% of treated patients and provided ment. Mayo Clin Proc 1995; 70:453–463.
pain relief in 84%–92% (68). Medical treatment 9. Scott RB, Te Linde RW. External endometriosis:
the scourge of the private patient. Ann Surg 1950;
is of value when the goal is to reduce pain and 131:697–720.
possibly diminish the anatomic extent of the dis- 10. Lloyd FP. Endometriosis in the Negro woman: a
ease (7). five year study. Am J Obstet Gynecol 1954; 89:
Conservative surgery can be performed with 468–469.
laparoscopy or laparotomy. The surgery is con- 11. Arumgam K, Lim JM. Menstrual characteristics as-
sociated with endometriosis. Br J Obstet Gynaecol
sidered conservative when reproductive function 1997; 104:948–950.
is retained. Success rates are believed to be high, 12. Ranney B. Endometriosis IV. Hereditary ten-
but implant recurrence develops in 28% of pa- dency. Obstet Gynecol 1971; 37:734–737.
tients at 18 months after surgery and in 40% by 9 13. Wellberry C. Diagnosis and treatment of endome-
years (69,70). Adhesions recur in 40%–50% of triosis. Am Fam Physician 1999; 60:1753–1768.
14. Thomas EJ. Endometriosis, 1995: confusion or
patients (71). The usefulness of conservative sur- sense? Int J Gynecol Obstet 1995; 48:149–155.
gery for improving fertility is controversial, but 15. Halme J, Hammond MG, Hulka JF, Raj SG,
since it has not been shown to be detrimental, Talvert LM. Retrograde menstruation in healthy
the procedure is commonly performed (7,13). women and in patients with endometriosis. Obstet
Women with infertility and endometriosis may be Gynecol 1984; 64:151–154.
16. Liu DTY, Hitchcock A. Endometriosis: its asso-
treated with advanced reproductive techniques ciation with retrograde menstruation, dysmenor-
such as ovarian hyperstimulation and intrauterine rhea, and tubal pathology. Br J Obstet Gynaecol
insemination and have monthly fecundity rates of 1986; 93:859–862.
9%–18% (72,73). 17. Blumenkrantz MJ, Gallagher N, Bashore RA,
Definitive surgery includes hysterectomy and Tenckhoff H. Retrograde menstruation in women
undergoing chronic peritoneal dialysis. Obstet
oophorectomy and is usually reserved for women Gynecol 1981; 57:667–670.
with intractable pain (74). In less severe cases, 18. Keetle WC, Stein RJ. The viability of the cast-off
one ovary may be retained. Endometriosis may menstrual endometrium. Am J Obstet Gynecol
recur with exogenous estrogen replacement thera- 1951; 61:440–442.
py, even in women who have undergone oopho- 19. Koninckx PR, Ide P, Vandenbroucke W, Brosens
IA. New aspects of the pathophysiology of endo-
rectomy (74). metriosis and associated infertility. J Reprod Med
1980; 24:257–260.
References 20. Jenkins S, Olive DL, Haney AF. Endometriosis:
1. Dmowski WP, Lesniewicz R, Rana N, Pepping P, pathogenic implications of the anatomic distribu-
Noursalehi M. Changing trends in the diagnosis of tion. Obstet Gynecol 1986; 67:335–338.
endometriosis: a comparative study of women with 21. Olive DL, Henderson DY. Endometriosis and
pelvic endometriosis presenting with chronic pelvic mullerian anomalies. Obstet Gynecol 1987; 69:
pain or infertility. Fertil Steril 1997; 67:238–243. 412–415.
2. Goldstein DP, deCholnoky C, Emans SJ, Leventhal 22. Clement PB. Diseases of the peritoneum. In:
JM. Laparoscopy in the diagnosis and management Kurman RJ, ed. Blaustein’s pathology of the female
of pelvic pain in adolescents. J Reprod Med 1989; genital tract. 4th ed. New York, NY: Springer-
24:251–256. Verlag, 1994; 660–680.
23. Oliker AJ, Harris AE. Endometriosis of the blad-
der in a male patient. J Urol 1971; 106:858–859.
24. Pinkert TC, Catlow CE, Straus R. Endometriosis
of the urinary bladder in a man with prostatic car-
cinoma. Cancer 1979; 43:1562–1567.
RG ■ Volume 21 • Number 1 Woodward et al 215
25. Merrill JA. Endometrial induction of endometri- 41. Filly RA. Ovarian masses…what to look for…what
osis across Millipore filters. Am J Obstet Gynecol to do. In: Callen PW, ed. Ultrasonography in ob-
1966; 94:780–790. stetrics and gynecology. 3rd ed. Philadelphia, Pa:
26. Oosterlynck DJ, Cornillie FJ, Waer M, Vande- Saunders, 1994; 625–640.
putte M, Koninckx PR. Women with endometri- 42. Togashi K, Nishimura K, Kimura I, et al. En-
osis show a defect in natural killer activity result- dometrial cysts: diagnosis with MR imaging. Radi-
ing in a decreased cytotoxicity to autologous endo- ology 1991; 180:73–78.
metrium. Fertil Steril 1991; 56:45–51. 43. Arrive L, Hricak H, Martin MC. Pelvic endometri-
27. Badawy SZA, Cuenca V, Stitzel A, Jacobs RDB, osis: MR imaging. Radiology 1989; 171:687–692.
Tomar RH. Autoimmune phenomenon in infertile 44. Dooms GC, Hricak H, Tscholakoff D. Adnexal
patients with endometriosis. Obstet Gynecol 1984; structures: MR imaging. Radiology 1986; 158:
63:271–275. 639–646.
28. Gompel C, Silverberg SG. The female peritoneum. 45. Sugimura K, Okizuka H, Imaoka I, et al. Pelvic en-
In: Pathology in gynecology and obstetrics. 4th ed. dometriosis: detection and diagnosis with chemical
Philadelphia, Pa: Lippincott, 1994; 425–431. shift MR imaging. Radiology 1993; 188:435–438.
29. Scully RE, Young RH, Clement PB. Tumor-like 46. Siegelman ES, Outwater EK. Tissue characteriza-
lesions. In: Tumors of the ovary, maldeveloped tion in the female pelvis by means of MR imaging.
gonads, fallopian tube, and broad ligament. Wash- Radiology 1999; 212:5–18.
ington, DC: Armed Forces Institute of Pathology, 47. Ascher SM, Agrawal R, Bis KG, et al. Endometri-
1998; 430–434. osis: appearance and detection with conventional
30. Crum CP. The female genital tract. In: Cortran and contrast-enhanced fat-suppressed spin-echo
RS, Kumar V, Collins T, eds. Robbins pathologic techniques. J Magn Reson Imaging 1995; 5:
basis of disease. 6th ed. Philadelphia, Pa: Saunders 251–257.
1999; 1057–1059. 48. Ha HK, Lim YT, Kim HS, Suh TS, Song HH,
31. Schenken RS. Endometriosis. In: Scott JR, Di Kim SJ. Diagnosis of pelvic endometriosis: fat-
Saia PJ, Hammond CB, Spellacy WN, eds. Dan- suppressed T1-weighted vs conventional MR im-
forth’s obstetrics and gynecology. 8th ed. Philadel- ages. AJR Am J Roentgenol 1994; 163:127–131.
phia, Pa: Lippincott Williams & Wilkins 1999; 49. Outwater EK, Dunton CJ. Imaging of the ovary
669–676. and adnexa: clinical issues and applications of MR
32. Foster DC, Stern JL, Buscema J, Rock JA, Wood- imaging. Radiology 1995; 194:1–18.
ruff JD. Pleural and parenchymal pulmonary en- 50. Thurmher S, Hudler J, Baer S, Maricek B, von
dometriosis. Obstet Gynecol 1981; 58:552–556. Schulthess GK. Gadolinium-DOTA enhanced
33. Thibodeau LL, Prioleau GR, Manuelidis EE, Me- MR imaging of adnexal tumors. J Comput Assist
rino MJ, Haefner MD. Cerebral endometriosis: Tomogr 1990; 14:939–949.
case report. J Neurosurg 1987; 66:609–610. 51. Bis KG, Vrachliotis TG, Agrawal R, Shetty AN,
34. Duke R, Fawcett P, Booth J. Recurrent subarach- Maximovich A, Hricak H. Pelvic endometriosis:
noid hemorrhage due to endometriosis. Neurology MR imaging spectrum with laparoscopic correla-
1995; 45:1000–1002. tion and diagnostic pitfalls. RadioGraphics 1997;
35. Redwine DB. Age related evolution in color ap- 17:639–655.
pearance of endometriosis. Fertil Steril 1987; 48: 52. Som PM, Dillon WP, Fullerton GD, Zimmerman
1062–1063. RA, Rajagopalan B, Marom Z. Chronically ob-
36. Revised American Fertility Society classification of structed sinonasal secretions: observation on T1
endometriosis: 1985. Fertil Steril 1985; 43:351–352. and T2 shortening. Radiology 1989; 172:515–520.
37. Patel MD, Feldstein VA, Chen DC, Lipson SD, 53. Dillon WP, Som PM, Fullerton GD. Hypointense
Filly RA. Endometriomas: diagnostic performance MR signal in chronically inspissated sinonasal se-
of US. Radiology 1999; 210:739–745. cretions. Radiology 1990; 174:73–78.
38. Guerriero S, Ajossa S, Paoletti AM, Mais V, 54. Sugimura K, Takemori M, Sugiura M, Okzuka H,
Angiolucci M, Melis GB. Tumor markers and Kono M, Ishida T. The value of magnetic reso-
transvaginal ultrasonography in the diagnosis of en- nance relaxation time in staging ovarian endome-
dometrioma. Obstet Gynecol 1996; 88:403–407. trial cysts. Br J Radiol 1992; 65:502–506.
39. Jain KA. Prospective evaluation of adnexal masses 55. Togashi K. Endometriosis. In: MRI of the female
with endovaginal gray-scale and duplex and color pelvis. Tokyo, Japan: Igaku-Shoin, 1993; 203–226.
Doppler US: correlation with pathologic findings. 56. Zawin M, McCarthy S, Scoutt LM, Comite F.
Radiology 1994; 191:63–67. Endometriosis: appearance and detection at MR
40. Volpi E, De Grandis T, Zuccaro G, La Vista A, imaging. Radiology 1989; 171:693–696.
Sismondi P. Role of transvaginal sonography in the
detection of endometriomata. J Clin Ultrasound
1995; 23:163–167.
216 January-February 2001 RG ■ Volume 21 • Number 1
57. Yantiss RK, Clement PB, Young RH. Neoplastic 66. Miller WB Jr, Melson GL. Abdominal wall endome-
and pre-neoplastic changes in gastrointestinal en- trioma. AJR Am J Roentgenol 1979; 132:467–468.
dometriosis. Am J Surg Pathol 2000; 24:513–524. 67. Walsh JW, Taylor KJW, Rosenfield AT. Gray
58. Scully RE, Young RH, Clement PB. Endometrioid scale ultrasonography in the diagnosis of endome-
tumors. In: Tumors of the ovary, maldeveloped go- triosis and adenomyosis. AJR Am J Roentgenol
nads, fallopian tube, and broad ligament. Wash- 1979; 132:87–90.
ington, DC: Armed Forces Institute of Pathology, 68. Bayer SR, Seibel MM. Medical treatment: danazol.
1998; 107–140. In: Schenken RS, ed. Endometriosis: contemporary
59. Scully RE, Young RH, Clement PB. Clear cell tu- concepts in clinical management. Philadelphia, Pa:
mors. In: Tumors of the ovary, maldeveloped go- Lippincott, 1989; 169–187.
nads, fallopian tube, and broad ligament. Wash- 69. Gordts S, Boeckx W, Brosens I. Microsurgery of
ington, DC: Armed Forces Institute of Pathology, endometriosis in infertile patients. Fertil Steril
1998; 141–152. 1984; 42:520–525.
60. Gedgaudas-McClees RK. Gastrointestinal compli- 70. Olive DL. Conservative surgery. In: Schenken RS,
cations of gynecologic diseases. In: Textbook of ed. Endometriosis: contemporary concepts in
gastrointestinal radiology. Philadelphia, Pa: clinical management. Philadelphia, Pa: Lippincott,
Saunders, 1994; 2559–2567. 1989; 213–247.
61. Zwas FR, Lyon DT. Endometriosis: an important 71. Vancaillie T, Schenken RS. Endoscopic surgery.
condition in clinical gastroenterology. Dig Dis Sci In: Schenken RS, ed. Endometriosis: contempo-
1991; 36:353–364. rary concepts in clinical management. Philadel-
62. Gordon RL, Evers K, Kressel HY, Laufer I, phia, Pa: Lippincott, 1989; 249–266.
Herlinger H, Thompson JJ. Double-contrast en- 72. Chaffkin LM, Nulsen LC, Luciano AA, Metzger
ema in pelvic endometriosis. AJR Am J Roent- DA. A comparative analysis of the cycle fecundity
genol 1982; 138:549–552. rates associated with combined human meno-
63. The urinary bladder. In: Dunnick NR, Sandler pausal gonadotropin (hMG) and intrauterine in-
CM, Amis ES, Newhouse JH, eds. Textbook of semination (IUI) versus either hMG or IUI alone.
uroradiology. 2nd ed. Baltimore, Md: Williams & Fertil Steril 1991; 55:252–257.
Wilkins, 1997; 396–439. 73. Dodson WC, Haney AF. Controlled ovarian hy-
64. Joseph J, Sahn SA. Thoracic endometriosis syn- perstimulation and intrauterine insemination for
drome: new observations from an analysis of 110 the treatment of infertility. Fertil Steril 1991; 55:
cases. Am J Med 1996; 100:164–170. 457–467.
65. Wolf C, Obrist P, Ensinger C. Sonographic fea- 74. Namnoum AB, Hickman TN, Goodman SB,
tures of abdominal wall endometriosis. AJR Am J Gehlbach DL, Rock JA. Incidence of symptom re-
Roentgenol 1997; 169:916–917. currence after hysterectomy for endometriosis.
Fertil Steril 1995; 64:898–902.
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