| Literature DB >> 19760524 |
Lohith S Bachegowda1, Gayathri Nagaraj, Petros D Grivas, Lingyi Chen, Eugene Choi, Michael Styler.
Abstract
Rhabdomyosarcoma (RMS) is the most common soft-tissue tumor in childhood, but is extremely rare in elderly. We present a rare case of cardiac RMS, which developed 1 year after the diagnosis and management of acute lymphoblastic leukemia in a 68-year-old female. The occurrence of such phenomena is intriguing, especially in an individual without prior history of malignancy at a younger age. Through the review of the existing literature, we attempt to approach the pathogenesis and clinical manifestations of this rare clinical entity.Entities:
Mesh:
Year: 2009 PMID: 19760524 DOI: 10.1007/s12032-009-9299-4
Source DB: PubMed Journal: Med Oncol ISSN: 1357-0560 Impact factor: 3.064