腹膜多囊间皮瘤1例

K. Tagore, R. Kumar, N. Bhavani, S. Ramachander
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引用次数: 0

摘要

腹膜多囊间皮瘤是一种罕见的间皮瘤,因其特有的组织学表现和良性表现而值得单独考虑。过去,这种病变常与囊性淋巴管瘤、肠系膜淋巴囊肿、弥漫性间皮瘤和播散性产黏液腺癌相混淆。由于复发率高,需要准确的诊断和长期随访。我们报告一个罕见的病例巨大的多囊腹膜间皮瘤在一个36岁的妇女。术后随访18个月,患者无症状,无进一步生长。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A case of multicystic peritoneal mesothelioma
Multicystic peritoneal mesothelioma is an unusual mesothelial lesion that deserves separate consideration because of its characteristic histologic picture and its benign behavior. In the past, this lesion was often confused with cystic lymphangioma, mesenteric lymphatic cyst, diffuse mesothelioma, and disseminated form of mucin-producing adenocarcinoma. Diagnostic accuracy and long-term follow-up are needed due to high incidence of recurrence. We report a rare case of huge multicystic peritoneal mesothelioma in a 36-year-old woman. At follow-up 18 months after surgery, the patient remained asymptomatic with no further growth.
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