| Literature DB >> 19547964 |
Françoise Rypens1, Laurent Garel, Julie Franc-Guimond, Hervé Sartelet.
Abstract
Pediatric paratesticular primary malignant tumors are rare, and most of them correspond to rhabdomyosarcomas (RMS). Paratesticular RMS has a better prognosis than RMS originating in other locations, because of its favorable histology and possible early diagnosis. The diagnosis relies upon the US findings of a paratesticular hypervascular mass in an adequate clinical setting. We report the unusual appearance of an infiltrating RMS tumor in a 3-year-old boy. The tumor presented as thickening of the tunica vaginalis. Atypical US appearance and discordance with clinical features caused suspicion of a tumoral process, allowing early diagnosis and treatment.Entities:
Mesh:
Year: 2009 PMID: 19547964 DOI: 10.1007/s00247-009-1315-5
Source DB: PubMed Journal: Pediatr Radiol ISSN: 0301-0449