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Multilocular cystic renal cell carcinoma: A case report and review of the literature
Author(s) -
Jia Hu,
Lü Jin,
Yifan Li,
Tao He,
Jiaju Liu,
Bentao Shi,
Shangqi Yang,
Yaoting Gui,
Xiangming Mao,
Yongqing Lai,
Liangchao Ni
Publication year - 2017
Publication title -
molecular and clinical oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.442
H-Index - 7
eISSN - 2049-9469
pISSN - 2049-9450
DOI - 10.3892/mco.2017.1526
Subject(s) - nephrectomy , renal cell carcinoma , medicine , pathological , renal mass , radiology , stage (stratigraphy) , cancer , kidney , pathology , paleontology , biology
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.

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