Mishra Shwetank, Awasthi Nipun, Hazra S P, Bera M K
Department of Urology, Institute of Post Graduate Medical Education and Research, Kolkata, West Bengal, India.
Saudi J Kidney Dis Transpl. 2015 Sep;26(5):996-9. doi: 10.4103/1319-2442.164590.
Primary synovial sarcoma (SS) of the kidney is a very rare disease as well as a diagnostic dilemma. Here, we present a case of a 60-year-old male clinically diagnosed as renal cell carcinoma. The radical nephrectomy specimen showed a well-circumscribed renal mass of approximately 13 cm × 9 cm × 7 cm. The cut-surface of the mass was tawny and firm, with cystic areas, and also showed focal hemorrhage and necrosis. Histologically, the tumor was composed of spindle cells arranged in the intersecting fascicles, alternating with hypocellular areas suggestive of monophasic synovial sarcoma. Morphological and immunohistochemical features were compatible with the diagnosis of SS of the kidney.
原发性肾滑膜肉瘤(SS)是一种极为罕见的疾病,也是一个诊断难题。在此,我们报告一例60岁男性患者,临床诊断为肾细胞癌。根治性肾切除标本显示一个边界清晰的肾脏肿块,大小约为13 cm×9 cm×7 cm。肿块切面呈黄褐色,质地坚硬,有囊性区域,还可见局灶性出血和坏死。组织学上,肿瘤由呈交叉束状排列的梭形细胞组成,与细胞稀少区域交替出现,提示为单相滑膜肉瘤。形态学和免疫组化特征与肾滑膜肉瘤的诊断相符。