A rare case of giant ovarian serous cystadenoma presenting as psuedo-meigs syndrome
Published on: 18th January, 2021
OCLC Number/Unique Identifier: 8897949620
Meigs’ syndrome is a rare condition characterized by the presence of a benign fibroma of the ovary, ascites and pleural effusion. Other benign cysts of the ovary (such as struma ovarii, mucinous cystadenoma, serous cystadenoma and teratomas), leiomyoma of the uterus, and secondary metastatic tumours to ovary if associated with hydro thorax and ascites are referred to as ‘Pseudo-Meigs” syndrome. It very uncommon and diagnosis is made difficult by symptoms that usually mimic disseminated malignancy or tuberculosis. The gold standard treatment is laparotomy and, by definition of the syndrome, after tumor removal, the symptoms resolves and the patients become asymptomatic. We presented an 18 years old girl with giant ovarian serous cystadenoma with associated pseudo-meigs syndrome, successfully managed in a low resources setting.
Giant hepatic cystadenoma mimicking a hydatid cyst: A challenging preoperative diagnosis
Published on: 24th March, 2021
OCLC Number/Unique Identifier: 8979497397
Biliary cystadenoma is a rare cystic tumor of the liver. It has a high recurrence rate and malignant transformation risk in middle-aged women. Pre-operative diagnosis is difficult because of the lack of clinical, biological and radiological specificity. The confirmation of the diagnosis is made by the histopathological examination. Complete surgical resection is preferred because of the high risk of malignant transformation and recurrence.
Huge Mucinous Cyst Adenoma, Case Report Series
Published on: 8th April, 2025
Mucinous cystadenoma constitutes 15% of epithelial ovarian tumors. In resource limited setting they may reach huge size as there is no regular medical checkup. This case series highlights these aspects along with diagnostic and surgical considerations.
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