| Literature DB >> 26029305 |
Brendan Wallace1, Michael Organ2, Scott Bagnell3, Ricardo Rendon4, Jennifer Merrimen4.
Abstract
We present a case of renal cell carcinoma (RCC) arising in a 26-year-old patient with a history of neuroblastoma. RCC after a previous diagnosis of neuroblastoma is very uncommon, and there have only been 23 reported cases. Using the results of our patient workup, we hoped to determine whether there was a genetic predisposition or iatrogenic cause for the RCC. There is no clear explanation why neuroblastoma survivors are prone to developing RCC. However, genetic predisposition and previous treatment likely play a role. Since there have been few cases described, and few investigations into the genetics of this subtype of RCC, it remains important for individual cases to be added to the literature of this recently described and rare entity.Entities:
Year: 2015 PMID: 26029305 PMCID: PMC4439234 DOI: 10.5489/cuaj.2564
Source DB: PubMed Journal: Can Urol Assoc J ISSN: 1911-6470 Impact factor: 1.862