Malignant fibrous histiocytoma of the kidney

Sunita Singh, Yashika Bhatia, J. Sharma, R. Sen
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Abstract

Primary renal malignant fibrous histiocytoma (MFH) is a rare tumor indistinguishable from renal cell carcinoma clinically and radiologically which can be differentiated only by histological and immunohistochemical studies. We report a case of primary renal MFH in a 40-year-old female who presented with left flank pain. Abdominal ultrasonography and computerized tomography revealed a well-defined renal mass. The contralateral kidney and renal functions were normal. Preoperative diagnosis was renal cell carcinoma and nephrectomy was performed. Histological examination and immunohistochemistry revealed MFH.
肾恶性纤维组织细胞瘤
原发性肾恶性纤维组织细胞瘤(MFH)是一种罕见的肿瘤,在临床和影像学上与肾细胞癌难以区分,只能通过组织学和免疫组织化学研究来鉴别。我们报告一例原发性肾MFH在一个40岁的女性谁提出了左侧疼痛。腹部超音波及电脑断层显示肾脏有明显肿块。对侧肾脏及肾功能正常。术前诊断为肾细胞癌,行肾切除术。组织学检查及免疫组化示MFH。
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