Puj Ketul S, Pandya Shashank J, Warikoo Vikas, Chauhan Tapansingh, Samanta Satarupa T
Department of Surgical Oncology, The Gujarat Cancer and Research Institute, Ahmedabad, India.
Department of Surgical Oncology, The Gujarat Cancer and Research Institute, Ahmedabad, India.
Urology. 2018 Jun;116:e7-e8. doi: 10.1016/j.urology.2017.12.017. Epub 2018 Mar 19.
Primary renal synovial sarcoma (PRSS) is a rare entity. It should be considered as one of the differential diagnoses of spindle cell tumors of the kidney. Immunohistochemistry and genetic translocation studies should be used to confirm the diagnosis. Because of a lack of consistent literature data regarding the treatment options, management of PRSS remains a therapeutic challenge. In view of the chemosensitive nature of the tumor, we propose a multimodality treatment in form of surgery and chemotherapy in patients with PRSS. Here we report a rare case of PRSS in a 17-year-old adolescent.
原发性肾滑膜肉瘤(PRSS)是一种罕见的疾病。它应被视为肾脏梭形细胞瘤的鉴别诊断之一。免疫组织化学和基因易位研究应用于确诊。由于缺乏关于治疗方案的一致文献数据,PRSS的管理仍然是一个治疗挑战。鉴于该肿瘤对化疗敏感的特性,我们建议对PRSS患者采用手术和化疗形式的多模式治疗。在此,我们报告一例17岁青少年患PRSS的罕见病例。