Gürocak Serhat, Sözen Sinan, Akyürek Nalan, Uluoğlu Omer, Alkibay Turgut
Department of Urology, Gazi University School of Medicine, Ankara, Turkey.
Urology. 2005 Jun;65(6):1226. doi: 10.1016/j.urology.2004.12.035.
Collecting duct carcinoma is a rare, highly aggressive, renal tumor arising from the distal collecting ducts. Various histologic patterns can be found in the same tumor but most demonstrate duct-like or papillary architecture surrounded by desmoplastic stroma. Grossly, these tumors are typically located in the medullary portion of the kidney near the region of the pelvis without extensive hemorrhage. It has a tendency to affect young patients and present at more advanced stages with a poorer prognosis. We describe a case of collecting duct carcinoma with histologic and immunohistochemical findings in a cortically located tumor.
集合管癌是一种罕见的、侵袭性很强的肾脏肿瘤,起源于远端集合管。同一肿瘤中可发现多种组织学模式,但大多数表现为被促纤维组织增生性间质包绕的导管样或乳头状结构。大体上,这些肿瘤通常位于肾脏髓质部分靠近肾盂区域,无广泛出血。它倾向于累及年轻患者,且多在晚期出现,预后较差。我们描述了一例位于皮质的集合管癌的组织学和免疫组化结果。