Torenbeek R, Blomjous C E, de Bruin P C, Newling D W, Meijer C J
Department of Pathology, Free University Hospital, Amsterdam, The Netherlands.
Am J Surg Pathol. 1994 Mar;18(3):241-9.
Sarcomatoid carcinoma is a rare tumor in the urinary bladder and accounts for approximately 0.3% of all bladder malignancies. In this study, the clinicopathologic findings of 18 cases are described. Distribution of sex and age and clinical symptoms are not distinctive from transitional cell carcinoma. The tumor behaves as a high-grade malignancy with advanced initial stage and unfavorable outcome. Surgery is the therapy of choice. Histological differentiation from true sarcoma may be difficult. Recognition rests on the co-existence of an overt carcinomatous component or demonstration of the epithelial nature by immunohistochemistry or electron microscopy.
肉瘤样癌是膀胱中的一种罕见肿瘤,约占所有膀胱恶性肿瘤的0.3%。在本研究中,描述了18例病例的临床病理特征。其性别、年龄分布及临床症状与移行细胞癌并无明显差异。该肿瘤表现为高级别恶性肿瘤,初始阶段即已进展,预后不良。手术是首选治疗方法。与真正的肉瘤进行组织学鉴别可能存在困难。诊断依赖于明显癌性成分的共存,或通过免疫组化或电子显微镜证实其上皮性质。