| Literature DB >> 23610735 |
Andrea Ferrari1, Cristina Meazza, Marco Vajna de Pava, Carlo Alfredo Clerici, Michela Casanova.
Abstract
This paper reports on two cases of adolescents with paratesticular embryonal rhabdomyosarcoma completely resected at diagnosis (a pediatric disease potentially curable in more than 90% of cases) and treated at adult facilities with a strategy used for adult soft tissue sarcomas. The final outcome of the two patients was dismal after they received a treatment inconsistent with pediatric protocols. The cases reported here give us a chance to turn the spotlight on a crucial issue-the referral of adolescents with pediatric-type tumors and their access to experienced centers and clinical trials.Entities:
Year: 2011 PMID: 23610735 PMCID: PMC3621802 DOI: 10.1089/jayao.2011.0016
Source DB: PubMed Journal: J Adolesc Young Adult Oncol ISSN: 2156-5333 Impact factor: 2.223