Göğüş Çağatay, Gökce Mehmet İlker, Süer Evren, Tulunay Özden, Şafak Mut
Department of Urology, Faculty of Medicine, Ankara University, Ankara, Turkey.
Department of Pathology, Faculty of Medicine, Ankara University, Ankara, Turkey.
Turk J Urol. 2013 Sep;39(3):194-7. doi: 10.5152/tud.2013.039.
We report a 44-year-old woman with a malignant fibrous histiocytoma (MFH) of the kidney. Primary renal MFH is an extremely rare tumor with a poor prognosis. Renal MFH is differentiated from renal cell carcinoma, renal sarcoma, and sarcomatoid renal tumors only by histological and immunohistochemical studies. Because the therapeutic options for MFH are different, its early diagnosis is imperative.
我们报告了一名44岁患有肾脏恶性纤维组织细胞瘤（MFH）的女性。原发性肾MFH是一种极其罕见且预后不良的肿瘤。肾MFH仅通过组织学和免疫组织化学研究与肾细胞癌、肾肉瘤及肉瘤样肾肿瘤相鉴别。由于MFH的治疗选择不同，早期诊断至关重要。
