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A Rare Case of Benign Multicystic Peritoneal Mesothelioma: A Clinical Dilemma

机译:良性多囊性腹膜间皮瘤罕见病例:临床 困境

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摘要

A middle aged housewife presented with an anterior abdominal wall mass which was slowly growing over a period of 1 years over the midline scar of previous caesarean section with cystic degeneration in a part of the tumor. Fine needle aspiration cytology revealed a papillary serous cystadenoma. At exploratory laparotomy tumor was seen arising from the ventral surface of the parietal peritoneum with normal viscera, omentum and ovaries. The pathologist reported the tumor as Benign Multicystic Peritoneal Mesothelioma. It is a rare but clinically favourable neoplasm with wide excision as the definitive treatment. Of the 130 cases reported in the literature, it has the least incidence in the Indian Subcontinent.
机译:一名中年家庭主妇出现前腹壁肿块,在过去的剖腹产中线瘢痕上生长了一段时间,并在肿瘤的一部分发生了囊性变性,并在1年内缓慢增长。细针穿刺细胞学检查发现乳头状浆液性囊腺瘤。在探索性剖腹手术中,观察到肿瘤来自顶腹膜腹面,内脏,大网膜和卵巢均正常。病理学家报告该肿瘤为良性多囊性腹膜间皮瘤。它是一种罕见的但临床上有利的肿瘤,具有广泛的切除性,可作为最终治疗方法。在文献报道的130例病例中,它在印度次大陆发病率最低。

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