Abstract
The lifetime risk of developing an ovarian malignancy is
reported to be 1.4% [1,2]. Invasive epithelial ovarian can-
cers have the highest prevalence in women between 60-64
years while germ cell or borderline tumours pre-dominate in
women under 40 years [2]. We report the case of a 33-year-
old nulliparous woman with a 7 kg leiomyoma, extensive
endometriosis and several radiological features suggestive
of a high stage ovarian malignancy. Meigs syndrome typi-
cally presents as a triad of ascites, pleural effusion and a
benign ovarian fibroma [3]. Psuedo-meigs syndrome differs
by presentation with ascites, pleural effusion and alterna -
tive benign tumours of the ovary such as mucinous cystad-
enomas, teratomas, struma ovarii and uterine leiomyomas
[4]. However, in this reported case we demonstrate normal
ovarian appearance and histology.
Keywords
Endometriosis, Ovarian cancer, Neoplasms, Leiomyoma,
Fibroid, Meigs syndrome
*Corresponding author: Dr. Cathy Monteith, PhD, Department of Gynaecology, St. James Hospital, Dublin, Ireland, Tel:
+353-14103000
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Meigs syndrome which differs in presentation with asci-
tes, pleural effusion and alternative benign tumours of
the ovary such as mucinous cystadenomas, teratomas,
struma ovarii or uterine leiomyomas [4]. Uterine leio -
myomas are the most common benign gynaecological
neoplasm with a reported lifetime risk of 30% [5].
Case Description
We present a 33-year-old nulliparous woman with a
previous history of midline laparotomy and right oopho-
rectomy in another institution for a ruptured Dermoid
cyst. She presented to our unit with a two year history
of progressive painless abdominal distension, weight
loss, bilateral pitting oedema and cyclical bleeding from
the umbilicus. She delayed seeking medical attention
as she was trying to conceive. On clinical examination
she was cachectic, had palpable cervical lymph nodes
and auscultation of the lungs demonstrated reduced air
entry. Palpation of abdomen revealed an irregular mass
arising from the right iliac fossa, non-mobile, extending
to the right upper quadrant and a second additional
separate cystic mass palpable in left abdominal wall.
Laboratory data were normal with the exception of ele-
vated Ca125 of 233.
A computed tomography (CT) revealed a large left
pleural effusion, a 26 × 16 × 31 cm solid heterogenous
mass with low attenuation areas suggestive of necrosis
and overall appearance suggestive of ovarian malignan-
Introduction
The lifetime risk of developing an ovarian malignancy
is reported to be 1.4% [1, 2]. Invasive epithelial ovarian
cancers have the highest prevalence in women between
60-64 years while germ cell or borderline tumours
pre-dominate in women under 40 years [2]. Meigs syn-
drome, first described by Meigs typically presents as a
triad of ascites, pleural effusion and a benign ovarian fi-
broma [3]. A similar presentation is described in pseudo
ISSN: 2377-9004
DOI: 10.23937/2377-9004/1410187
Monteith et al. Obstet Gynecol Cases Rev 2020, 7:187
• Page 2 of 5 •
stage (Stage III or IV) of disease in two thirds of cases
with associated ascites or pleural effusions [2].
The aetiology of the observed ascites and pleural ef-
fusion in Meigs or Psuedo Meigs syndrome is unclear.
The suggested mechanisms have included hypo albu -
minemia, peritoneal irritation, lymphatic obstruction,
release of toxins or inflammatory mediators [6]. There
is limited literature surrounding fertility conservation in
the setting of Meigs syndrome including those occurring
in paediatric cases [7]. The attainment of a presurgical
diagnosis of Meigs or Psuedo Meigs syndrome remains
challenging especially in the setting of an elevated Ca
125.
Ca 125 is a glycoprotein which was first associated
and measured as a marker for established ovarian can-
cer in the early 1980s [8]. While it does not offer a role
in screening for ovarian cancer, a serum Ca 125 level is
a vital component of the risk of malignancy index (RMI)
which is used to triage cases of suspected malignancy.
An increased serum Ca 125 has shown ethic variation
with higher levels in Caucasian women when compared
to Black or Asian women. The following conditions have
also demonstrated increased serum Ca 125 levels: Pel-
vic inflammatory disease, fibroids, cyst accident, en-
dometriosis, tuberculosis, cirrhosis, ascites, hepatitis,
pancreatitis and pleuritis. Elevated levels have also
been demonstrated in primary breast, pancreas, lung
cy. In addition, there were multiple calcified lesions es-
pecially in the right upper quadrant abutting the liver
representing possible metastatic deposits. There was
large volume ascites and a 19 × 4 cm fluid collection in
the left anterior abdominal wall.
A pleuritic drain was inserted and yielded serous
fluid with cytology negative for malignancy and pelvic
biopsy showed no evidence of necrosis, atypia or in -
creased mitoses and was in keeping with a smooth mus-
cle lesion likely representing a benign leiomyoma. With
the clinical and radiological suspicions, the gynaecology
multidisciplinary meeting recommended progressing
surgery with pre-operative insertion of right ureteric
stent, interval reduction in pleural effusion, coagulation
specialist opinion regarding insertion of a prophylactic
IVC filter (advised prophylactic heparin only) and pro-
phylactic uterine artery embolization which was per-
formed six days pre-operatively.
The team proceeded to a total abdominal hysterec -
tomy due to grossly distorted uterus inseparable from 7
kg mass, left salpingectomy, biopsy and conservation of
left ovary due to normal gross appearance, appendec -
tomy, excision of presumed abdominal wall seroma, in-
fra-colic omentectomy, refashioning of abdominal wall,
drainage of 2.6 L ascites, estimated blood loss 1000 ml.
Intra-operative ascitic fluid was negative on cytology
for malignancy. Histopathology reported a 28 cm leio -
myoma with hyalinization, ischaemic necrosis second -
ary to embolization and extensive adenomyosis. There
was extensive endometriosis of the anterior abdominal
wall, umbilicus, omentum and seroma with endometri-
otic cyst formation. The perihepatic calcifications were
blood clot associated with aggregated macrophages,
acute inflammatory cells and fragments of mesotheli -
um. Left ovarian biopsy demonstrated normal ovarian
stroma with no evidence of endometriosis and similarly
normal assessment of the appendix and left fallopian
tube.
The early post-operative course was complicated
with a third order pulmonary embolism and transfusion
of four units red cells to correct anaemia. The ureteric
stent was removed at three months post-operatively. At
the six month post-operative review the patient report-
ed an uncomplicated physical recovery with appropriate
weight gain, healthy appearance, laboratory confirma-
tion of preserved ovarian function with anti-mullerian
hormone of 24 and satisfactory cosmetic result of ab-
domen. She was discharged at that visit to her general
practitioner and a reproductive counsellor.
Conclusion
Ovarian cancer remains one of the most frequent
causes of death at 47% of all deaths from cancers of the
female genital tract [2]. Women with ovarian cancer of-
ten report only vague symptoms of bloating, abdominal
distension and as a result frequently present at a late
Figure 1: Pre-operative CT imaging of a patient with
Psuedo-Meigs Syndrome.
ISSN: 2377-9004
DOI: 10.23937/2377-9004/1410187
Monteith et al. Obstet Gynecol Cases Rev 2020, 7:187
• Page 3 of 5 •
There have been previous reported cases of Pseudo
Meigs syndrome secondary to uterine leiomyomas with
reported elevated Ca 125 ranging between 83-1854
[6,9]. There have been previous case reports of ascites
+/- pleural effusion in the setting of endometriosis. In
those cases the ascitic or pleuritic fluid was frequently
reported as blood stained with the haemosiderin con -
tent making interpretation of fluid cytology challenging
[10]. Our reported case is unique and is in contrast to
the prior reports of pseudo Meigs syndrome describing
multiple pathologies of leiomyoma, adenomyosis and
extensive endometriosis. In addition, our presented
case highlights that in the setting of benign fluid cytol-
ogy and benign pelvic biopsy that fertility conserving
surgery is a reasonable alternative (Figure 1, Figure 2,
Figure 3, Figure 4, Figure 5, Figure 6, Figure 7, Figure 8, or colon cancers where there is presence of peritoneal
metastasis.
Figure 2: Pre-operative fluoroscopy at time of fibroid
embolisation in a patient with Psuedo-Meigs Syndrome.
Figure 3: Pre-operative examination of a patient with
Psuedo-Meigs Syndrome.
Figure 4: Pre-operative clinical examination (lateral
view) of a patient with Psuedo-Meigs Syndrome.
Figure 5: Intra-operative Pelvic mass.
ISSN: 2377-9004
DOI: 10.23937/2377-9004/1410187
Monteith et al. Obstet Gynecol Cases Rev 2020, 7:187
• Page 4 of 5 •
Authors Declaration
All authors have had equal contribution to this sub -
mission and all authors report no conflicts of interest.
Figure 9 and Figure 10).
Funding
No funding sources for this submission.
Figure 6: Intra-operative peri-hepatic calcified lesions.
Figure 7: Left abdominal wall subcuticular seroma/
Endometriotic cyst capsule.
Figure 8: Excised pelvic mass Anterior view.
Figure 9: Excised pelvic mass Posterior view.
ISSN: 2377-9004
DOI: 10.23937/2377-9004/1410187
Monteith et al. Obstet Gynecol Cases Rev 2020, 7:187
• Page 5 of 5 •
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Figure 10: Three month post-operative abdominal
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