| Literature DB >> 12652340 |
J George1, G Stacy, T Peabody, A Montag.
Abstract
Rosai-Dorfman disease is a rare entity predominantly affecting children and young adults, characterized in 83-95% of cases by painless bilateral cervical lymphadenopathy. We report the unusual case of a 41-year-old woman with Rosai-Dorfman disease that presented as a solitary lesion of the radius without other clinical manifestations.Entities:
Mesh:
Year: 2003 PMID: 12652340 DOI: 10.1007/s00256-002-0613-x
Source DB: PubMed Journal: Skeletal Radiol ISSN: 0364-2348 Impact factor: 2.199