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 manifestation.
- Rosai-Dorfman disease
- Solitary lesion
ASJC Scopus subject areas
- Radiology Nuclear Medicine and imaging