腹膜后肉样瘤病的罕见病例

Soufiane Habyebete, Ahmed Ameziane, Ali Akjay, Khalid Lmezguidi, A. Ammani, J. Anzaoui
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引用次数: 0

摘要

肉样瘤病是一种病因未明的全身性肉芽肿病,其特点是受累器官形成上皮样和巨大细胞肉芽肿,但无病例坏死。我们的病例有肉样瘤病史,并伴有左侧腹痛。CT 扫描发现左肾积水,继发于腹膜后肿块包裹腰部输尿管,该肿块被双 J 支架分流。肿块活检显示纤维组织伴有上皮样和巨大细胞肉芽肿,但无病例性坏死。我们的病人是一例极为罕见的病例报告。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Rare Case of Retroperitoneal Sarcoidosis
Sarcoidosis is a systemic granulomatosis of undetermined etiology characterised by the formation of epithelioid and gigantocellular granulomas without caseous necrosis in the affected organs. Our case has a history of sarcoidosis with left flank pain. CT scan founded a left hydronephrosis secondary to a retroperitoneal mass encasing the lumbar ureter which was shunted by a double j stent. Biopsy of the mass showed fibrous tissue with epithelioid and gigantocellular granuloma without caseous necrosis. Our patient is an extremely rare case report.
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