| Literature DB >> 830977 |
Abstract
Embryonal rhabdomyosarcoma of the prostate is typically a rare mesenchymal tumor of young boys, presenting with obstructive urinary symptoms or an abdominal mass. The origin is probably in undifferentiated mesenchymal cells that persist into adult life. Histologically, the tumor cells resemble normal muscle development in a 7 to 10-week fetus. Treatment is combined radical surgery and chemotherapy, and usually radiotherapy as well. The prognosis is extremely poor in all patients. Our case is added to the few in the literature in which this disease occurred in a man more than 50 years old.Entities:
Mesh:
Year: 1977 PMID: 830977 DOI: 10.1016/s0022-5347(17)58351-2
Source DB: PubMed Journal: J Urol ISSN: 0022-5347 Impact factor: 7.450