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Multilocular cystic renal cell carcinoma: a rare entity with review of literature.
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Arch Iran Med. 2014 Feb;17(2):129-32.
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多房性囊性肾细胞癌:一例报告并文献复习

Multilocular cystic renal cell carcinoma: A case report and review of the literature.

作者信息

Hu Jia, Jin Lu, Li Yifan, He Tao, Liu Jiaju, Shi Bentao, Yang Shangqi, Gui Yaoting, Mao Xiangming, Lai Yongqing, Ni Liangchao

机构信息

Department of Urology, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.

Graduate School of Guangzhou Medical University, Guangzhou, Guangdong 510182, P.R. China.

出版信息

Mol Clin Oncol. 2018 Feb;8(2):326-329. doi: 10.3892/mco.2017.1526. Epub 2017 Dec 8.

DOI:10.3892/mco.2017.1526
PMID:29435299
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5776426/
Abstract

Multilocular cystic renal cell carcinoma (MCRCC), which exhibits low-stage and low-grade characteristics, is a special type of RCC. MCRCC is extremely rare and generally develops at ages >50 years. We herein report a case of MCRCC in a 28-year-old man, which, to the best of our knowledge, is the youngest case reported worldwide to date. The patient presented with irritative bladder symptoms for 1 year. Dynamic enhanced computed tomography (CT) imaging revealed a mass with inhomogeneous enhancement in the left kidney, with a rich blood supply. B-ultrasonography also revealed a renal protruding mass. As the mass was highly suspicious to be a malignant tumor, laparoscopic radical nephrectomy was performed and MCRCC was definitively diagnosed by pathological examination. The patient has been regularly followed up for 6 months, without complications or disease recurrence.

摘要

多房囊性肾细胞癌(MCRCC)是肾细胞癌的一种特殊类型,具有低分期和低分级的特点。MCRCC极为罕见,通常发生于50岁以上人群。我们在此报告一例28岁男性的MCRCC病例,据我们所知,这是迄今为止全球报道的最年轻病例。该患者出现刺激性膀胱症状1年。动态增强计算机断层扫描(CT)成像显示左肾有一个不均匀强化的肿块,血供丰富。B超检查也显示有一个肾突出肿块。由于该肿块高度怀疑为恶性肿瘤,遂行腹腔镜根治性肾切除术,病理检查确诊为MCRCC。患者已定期随访6个月,无并发症或疾病复发。