A Rare Case of Giant Ovarian Serous Cystadenoma presenting as Psuedo-Meigs Syndrome

Richmond Ronald Gomes
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Abstract

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.
一例罕见的巨大卵巢浆液性囊腺瘤表现为假meigs综合征
梅格斯综合征是一种罕见的病症,其特征是卵巢良性纤维瘤、腹水和胸腔积液。其他良性卵巢囊肿(如卵巢瘤、粘液性囊腺瘤、浆液性囊腺瘤和畸胎瘤)、子宫平滑肌瘤和继发性卵巢转移瘤(如果伴有胸水和腹水)被称为“伪Meigs”综合征。它非常罕见,诊断困难,症状通常类似播散性恶性肿瘤或结核病。金标准治疗是开腹手术,根据综合征的定义,肿瘤切除后,症状消退,患者无症状。我们报告了一位18岁的女孩,患有巨大卵巢浆液性囊腺瘤并伴有伪meigs综合征,在低资源环境下成功治疗。
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