Renal Leiomyosarcoma, a Rare Presentation

IF 1.9 Q3 ONCOLOGY
T. Djiwa, K. Sabi, P. Simgban, Mayi Bombonne, B. Sama, Mazamaesso Tchaou, T. Darré
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引用次数: 1

Abstract

Renal sarcomas are very rare malignant tumours with a very poor prognosis. Renal leiomyosarcoma, a malignant tumour of smooth muscle origin, is the most common histological type. The article reports a case of leiomyosarcoma of renal location, with a review of the literature. A 38-year-old female patient, with no previous pathological history, consulted the nephrology department of the Teaching Hospital of Lomé for abdominal pain that had been present for 4 years. Histology showed a tumour proliferation of fasciculated architecture, made of spindle cells arranged in long bundles, with cytonuclear atypia and cytoarchitectural abnormalities. Immunohistochemical examination showed positive staining for smooth muscle actin, h-caldesmone, desmin and CD34 and negative for pancytokeratin (AE1/AE3), myogenin and PS100. Renal leiomyosarcoma is an exceptional malignancy. It remains the most common renal sarcoma, the differential diagnosis of which is based on immunohistochemical findings.
肾脏平滑肌肉瘤,一种罕见的表现
肾肉瘤是一种非常罕见的恶性肿瘤,预后很差。肾平滑肌肉瘤是一种起源于平滑肌的恶性肿瘤,是最常见的组织学类型。本文报告1例肾脏部位平滑肌肉瘤,并复习文献。38岁女性患者,既往无病理史,因腹痛4年就诊lomoise教学医院肾脏病科。组织学显示肿瘤呈束状结构增生,由长束排列的梭形细胞组成,具有细胞核异型性和细胞结构异常。免疫组化检查显示平滑肌肌动蛋白、h- caldesmoone、desmin和CD34阳性,全细胞角蛋白(AE1/AE3)、肌原蛋白和PS100阴性。肾平滑肌肉瘤是一种罕见的恶性肿瘤。它仍然是最常见的肾肉瘤,其鉴别诊断是基于免疫组织化学结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
自引率
6.20%
发文量
22
审稿时长
4 weeks
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