Rosai-Dorfman disease manifesting as a solitary lesion of the radius in a 41-year-old woman.

George, J; Stacy, G; Peabody, T; Montag, A · Skeletal Radiol · 2003

case_report · Level V

Where this comes from

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.

Medical subject headings

Anatomy