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以基底样鳞状细胞癌成分为主的肉瘤样癌:输尿管罕见双相肿瘤的首例报告

Sarcomatoid carcinoma with a predominant basaloid squamous carcinoma component: the first report of an unusual biphasic tumor of the ureter.

作者信息

Maeda Daichi, Fujii Akiko, Yamaguchi Kazumi, Tominaga Takashi, Fukayama Masashi, Mori Masaya

机构信息

Department of Pathology, Faculty of Medicine, University of Tokyo, 7-3-1 Hongo Bunkyo-ku, Tokyo 113-0033, Japan.

出版信息

Jpn J Clin Oncol. 2007 Nov;37(11):878-83. doi: 10.1093/jjco/hym120.

Abstract

Malignant tumors of the ureter that display biphasic patterns are very rare; they include carcinosarcomas, sarcomatoid carcinomas and carcinomas with pseudosarcomatous stroma. Although the distinction between carcinosarcomas and sarcomatoid carcinomas has been extensively discussed in the past, the recent World Health Organization classification of urinary tract tumors (2004) does not distinguish the two lesions and use the term sarcomatoid carcinoma to represent these biphasic tumors. The epithelial components of previously reported ureteral biphasic tumors comprise transitional cell carcinoma, squamous cell carcinoma, carcinoma in situ, small cell carcinoma and adenocarcinoma. In this paper, we report the first case of sarcomatoid carcinoma of the ureter with a predominant basaloid squamous carcinoma component. A 63-year-old man who had developed asymptomatic gross hematuria was diagnosed with a right ureteral tumor and underwent a right nephroureterectomy. Macroscopic examination of the excised tumor revealed a polypoid mass. Histopathologic examination exposed a tumor with malignant epithelial and sarcomatous components. The malignant epithelial component was predominantly composed of basaloid squamous carcinoma, and the sarcomatous component was mostly composed of undifferentiated spindle cells. A small focus of a chondrosarcomatous component was present. There were also transitional zones between the two components. In addition, the spindle cells of the sarcomatous component were partially positive for cytokeratin 7. We believe that the findings of this case study will increase the morphological diversity used for diagnosing malignant tumors of the ureter.

摘要

呈现双相模式的输尿管恶性肿瘤非常罕见;它们包括癌肉瘤、肉瘤样癌以及伴有假肉瘤性间质的癌。尽管过去已对癌肉瘤和肉瘤样癌之间的区别进行了广泛讨论,但世界卫生组织最近的泌尿道肿瘤分类(2004年)并未区分这两种病变,而是使用肉瘤样癌这一术语来代表这些双相肿瘤。先前报道的输尿管双相肿瘤的上皮成分包括移行细胞癌、鳞状细胞癌、原位癌、小细胞癌和腺癌。在本文中,我们报告了首例以基底样鳞状癌成分为主的输尿管肉瘤样癌病例。一名63岁男性出现无症状肉眼血尿,被诊断为右侧输尿管肿瘤并接受了右侧肾输尿管切除术。对切除肿瘤的宏观检查显示为息肉样肿块。组织病理学检查发现肿瘤具有恶性上皮和肉瘤成分。恶性上皮成分主要由基底样鳞状癌组成,肉瘤成分大多由未分化的梭形细胞组成。存在一小灶软骨肉瘤成分。此外,两种成分之间还有过渡区域。另外,肉瘤成分的梭形细胞部分细胞角蛋白7呈阳性。我们认为本病例研究的结果将增加用于诊断输尿管恶性肿瘤的形态学多样性。

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