| Literature DB >> 15882748 |
Stanley Zaslau1, Adam E Perlmutter, Hesam Farivar-Mohseni, William W L Chang, Stanley J Kandzari.
Abstract
Paratesticular rhabdomyosarcomas are rare tumors with aggressive growth patterns. Multimodal therapy with surgery, chemotherapy, and radiotherapy provides the patient with an excellent long-term prognosis. These tumors often present in the first two decades after birth. We report on the case of an 18-year-old man with a paratesticular rhabdomyosarcoma.Entities:
Mesh：
Year: 2005 PMID： 15882748 DOI： 10.1016/j.urology.2004.11.004
Source DB: PubMed Journal: Urology ISSN： 0090-4295 Impact factor: 2.649