| Literature DB >> 31969398 |
Jessica Connor1, Johnson F Tsui2, Wenlei He3, Ravi Munver4,2.
Abstract
Adult renal rhabdomyosarcoma (RMS) is a rare and aggressive entity with a paucity of data and reports in the literature. As a result, treatment guidelines for this malignancy are not well-established. Herein, we present the diagnosis, management and clinical course of a 39-year-old patient diagnosed with primary renal embryonal RMS (ERMS) following radical nephrectomy. We also review the existing literature on primary renal ERMS. © BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: pathology; urological cancer
Mesh:
Year: 2020 PMID: 31969398 PMCID: PMC7021188 DOI: 10.1136/bcr-2019-231000
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X