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Malignant fibrous histiocytoma arising from renal capsule: An extremely rare entity

机译:肾囊引起的恶性纤维组织细胞瘤:极为罕见的实体

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Malignant fibrous histiocytoma (MFH) usually presents in the extremities or retroperitoneum. MFH arising from renal parenchyma or renal capsule is extremely rare, only few cases have been reported in literature and portend a poor prognosis. Renal MFH is differentiated from renal cell carcinoma, renal sarcoma, and sarcomatoid renal tumor only by histological and immunohistochemical studies. Since the therapeutic options for MFH are different, its early diagnosis is imperative. Herein, we report a case of a primary renal MFH in a 35-year-old male.
机译:恶性纤维组织细胞瘤(MFH)通常存在于四肢或腹膜后。由肾实质或肾囊引起的MFH极为罕见,文献报道只有少数病例,预后不良。仅通过组织学和免疫组织化学研究,肾MFH才与肾细胞癌,肾肉瘤和肉瘤样肾肿瘤区分开。由于MFH的治疗选择不同,因此必须尽早诊断。在此,我们报告了一名35岁男性的原发性肾MFH病例。

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