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Sarcomatoid carcinoma of the urinary tract
Authors:Tetsuya Murata  Toshihiko Soga  Kazuhiro Tajima  Kaoru Saito  Yoshinori Komeda  Sergio Ossamu Loshii  Taizo Shiraishi  Teruyo Sakakura   Ryuichl Yatani
Affiliation:Divisions of Pathology, JA Suzuka Hospital, Suzuka;Divisions of Urology, JA Suzuka Hospital, Suzuka;Division of Urology, Hazu Hospital, Yokkaichi;Department of Pathology, Mie University School of Medicine, Tsu;Laboratory of Cell Biology, Riken, Tsukuba, Japan
Abstract:Sarcomatoid carcinoma is a rare variant of malignant tumor arising from the urinary tract. This tumor had been termed carcinosarcoma because of its carcinomatous and sarcomatous components. There is still some confusion in the terminology between true carcinosarcoma and sarcomatoid carcinoma; however, the latter is now regarded as primarily a malignant epithelial tumor with pseudosarcomatous transformation.
Four cases of sarcomatoid carcinoma arising from the urinary tract are reported. The patients were a 77 year old female, and three males aged 62, 69 and 80 years. All but the eldest patient complained of gross hematurla. Surgical removal was performed in the younger three cases, and an autopsy was done in the remaining case. All the tumors were macroscopically polypoid. Histopathologic examination revealed fasciculated spindle-cell tumors with myxold stroma or malignant fibrous histiocytoma-like spindle cell tumors. The epithelial nature was proven in these sarcomatous cells by immunohistochemical andlor electron-microscopic examinations. Only a small amount of squamous cell carcinoma components was also evident in the latter three cases. Although the younger three patients were alive at 44, 23 and 39 months'follow-up, respectively, constant careful monitoring Is recommended.
Keywords:sarcomatoid carcinoma    urinary tract
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