A Pelvic Mass Masquerading as High Stage Malignancy - An Interesting Presentation of Psuedo-Meigs Syndrome

In: Obstetrics and Gynaecology Cases - Reviews · 2020 · vol. 7(6) · doi:10.23937/2377-9004/1410187 · W3116105969
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This case report describes a 33-year-old woman whose large uterine leiomyoma with endometriosis mimicked advanced ovarian malignancy due to ascites and pleural effusion, resembling Pseudo-Meigs syndrome.

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This case report describes a 33-year-old woman presenting with symptoms and radiological features mimicking high-stage ovarian malignancy, including ascites, pleural effusion, elevated CA125, and a large pelvic mass. Surgical intervention revealed that the mass was actually a benign leiomyoma associated with extensive endometriosis and adenomyosis, confirming a diagnosis of pseudo-Meigs syndrome rather than cancer. The study highlights that benign conditions like leiomyomas can produce malignant-appearing clinical signs and notes that fertility-conserving surgery is a viable option when cytology excludes malignancy. Relevance to endometriosis: listed as one indication for GnRH antagonists, though the paper's main focus is uterine fibroids.

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Abstract

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 typically presents as a triad of ascites, pleural effusion and a benign ovarian fibroma
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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 Check for updates 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 •

References

1. Gaughan EMG, Walsh TA (2014) Risk-reducing surgery for women at high risk of epithelial ovarian cancer. The Obste- trician & Gynaecologist 16: 185-191. 2. Berek JS, Kehoe ST, Kumar L, Friedlander M (2018) Can- cer of the ovary, fallopian tube, and peritoneum. Int J Gy- naecol Obstet 143: 59-78. 3. Meigs JV (1954) Fibroma of the ovary with ascites and hydrothorax; Meigs’ syndrome. Am J Obstet Gynecol 67: 962-985. 4. Peparini N, Chirletti P (2009) Ovarian malignancies with cytologically negative pleural and peritoneal effusions: De- mons’ or meigs’ pseudo-syndromes? Int J Surg Pathol 17: 396-397. 5. Younas K, Hadoura E, Majoko F, Bunkheila A (2016) A review of evidence-based management of uterine fibroids. The Obstetrician & Gynaecologist 18: 33-42. 6. Dong RY, Jin CJ, Zhang Q, Yang XS, Kong BH (2015) Cellular leiomyoma with necrosis and mucinous degener - ation presenting as pseudo-Meigs’ syndrome with elevated CA125. Oncol Rep 33: 3033-3037. 7. Fremed MA, Levin TL, Sun KY, Weiser DA (2015) Ovary preservation in the treatment of childhood Meigs syndrome. Pediatr Blood Cancer 62: 2011-2014. 8. Bast RC, Klug TL, St John E, Jenison E, Niloff JM, et al. (1983) A radioimmunoassay using a monoclonal antibody to monitor the course of epithelial ovarian cancer. N Engl J Med 309: 883-887. 9. Adlan A-S, Chua PT, Huang K-G (2010) Laparoscopic resection of a subserosal leiomyoma presenting as pseu- do-meigs’ syndrome. Journal of Gynecologic Surgery 36: 222-225. 10. Gungor T, Kanat-Pektas M, Ozat M, Zayifoglu Karaca M (2011) A systematic review: Endometriosis presenting with ascites. Arch Gynecol Obstet 283: 513-518. Figure 10: Three month post-operative abdominal examination of a patient with Psuedo-Meigs Syndrome.

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