Pacchioni Donatella, Bosco Martino, Allia Elena, Mussa Baudolino, Mikuz Gregor, Bussolati Gianni
Department of Biomedical Sciences and Human Oncology, University of Turin, via Santena 7, 10126, Turin, Italy.
Virchows Arch. 2009 Feb;454(2):223-7. doi: 10.1007/s00428-008-0693-7. Epub 2008 Nov 11.
Microcystic urothelial cell carcinoma is a rare variant of urothelial cell carcinoma which occurs in the bladder and, rarely, in the renal pelvis. Neuroendocrine differentiation is uncommon in pure urothelial carcinoma and is more frequently found in neoplasms with glandular differentiation. We report a case of microcystic urothelial cell carcinoma arising in renal pelvis and showing focal neuroendocrine differentiation. A 55-year-old man with a history of non-small cell cancer of the lung presented with abdominal pain and hematuria. Imaging studies and gross examination revealed a partially cystic mass in the left kidney. Microscopic examination disclosed invasive carcinoma with prominent microcystic features, with microcysts lined by low columnar and flat cells. Immunohistochemical analysis confirmed the urothelial histotype (positive for thrombomodulin, p63 and high-molecular-weight cytokeratins) and disclosed focal neuroendocrine differentiation.
微囊性尿路上皮癌是尿路上皮癌的一种罕见变体,发生于膀胱,很少见于肾盂。神经内分泌分化在单纯尿路上皮癌中不常见,而在有腺性分化的肿瘤中更常见。我们报告一例发生于肾盂并表现为局灶性神经内分泌分化的微囊性尿路上皮癌。一名有非小细胞肺癌病史的55岁男性,因腹痛和血尿就诊。影像学检查和大体检查发现左肾有一个部分囊性肿物。显微镜检查显示为具有显著微囊性特征的浸润性癌,微囊肿内衬低柱状和平坦细胞。免疫组化分析证实为尿路上皮组织学类型(血栓调节蛋白、p63和高分子量细胞角蛋白阳性),并显示局灶性神经内分泌分化。