Nagayoshi J, Kawakami T, Maruyama Y
Department of Urology, Matsusaka Chuo Hospital, Mie, Japan.
Int J Urol. 1997 Nov;4(6):618-20. doi: 10.1111/j.1442-2042.1997.tb00321.x.
We report a case of sarcomatoid carcinoma of the ureter in a 60-year-old woman who presented at our hospital with right flank pain. She had undergone total ovariectomy and radiation therapy for ovarian cancer at the age of 40 years. A diagnosis of ureteral tumor (cTsN0M0) led to radical right nephroureterectomy and partial cystectomy. Microscopic examination showed a tumor that contained areas of both sarcoma and transitional cell carcinoma. The carcinomatous tissues were blended into the sarcomatous areas and there was a transitional zone between the 2 components. Immunohistochemical examination showed that the spindle cells were positive for cytokeratin, so the final diagnosis was sarcomatoid carcinoma of the ureter. The patient has remained well without any evidence of recurrence for 5 months since the operation. There is no effective adjunctive therapy, so constant careful monitoring will be necessary. Sarcomatoid carcinoma of the ureter is a rare tumor and this is only the sixth case reported in Japan.
我们报告一例60岁女性输尿管肉瘤样癌病例,该患者因右侧腰痛前来我院就诊。她在40岁时因卵巢癌接受了全卵巢切除术和放射治疗。输尿管肿瘤(cTsN0M0)诊断后,患者接受了根治性右肾输尿管切除术和部分膀胱切除术。显微镜检查显示肿瘤包含肉瘤和移行细胞癌区域。癌组织与肉瘤区域混合,两者之间有一个过渡区。免疫组化检查显示梭形细胞细胞角蛋白阳性,因此最终诊断为输尿管肉瘤样癌。自手术以来,患者已健康存活5个月,无任何复发迹象。由于没有有效的辅助治疗方法,因此需要持续密切监测。输尿管肉瘤样癌是一种罕见肿瘤,这是日本报告的第六例病例。