Haitel A, Wiener H G, Susani M
Department of Pathology, University of Vienna, Austria.
Pathol Res Pract. 1996 Jan;192(1):81-5; discussion 86-7. doi: 10.1016/S0344-0338(96)80140-3.
Genuine adenocarcinomas of the ureter are rare tumors and have to be distinguished from other gland-forming malignancies arising from the transitional epithelium, due to the poor clinical outcome. The histopathological features of a tumor combined with intestinal metaplasia of the adjacent urothelium are described. The tumor has to be distinguished from transitional cell cancer with glandular metaplasia, muco-urothelial cancer, microcystic transitional cell cancer and transitional cell cancer with mucoid cytoplasmatic inclusions. Immunohistochemical analysis of the cancer shows positivity for carcinoembryonic antigen and a staining pattern characteristic for adenocarcinomas. The expression of keratin types 7 and 13, which is typically found in transitional cell carcinomas, is lost.
输尿管原发性腺癌是罕见肿瘤,由于临床预后较差,必须与起源于移行上皮的其他腺形成性恶性肿瘤相鉴别。本文描述了一例伴有相邻尿路上皮肠化生的肿瘤的组织病理学特征。该肿瘤必须与伴有腺化生的移行细胞癌、黏液性尿路上皮癌、微囊性移行细胞癌以及伴有黏液样胞质包涵体的移行细胞癌相鉴别。对该癌进行免疫组织化学分析显示癌胚抗原呈阳性,且具有腺癌特有的染色模式。在移行细胞癌中通常可见的角蛋白7和13的表达缺失。