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

J. George, G. Stacy*, T. Peabody, A. Montag

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

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 manifestation.

Original languageEnglish (US)
Pages (from-to)236-239
Number of pages4
JournalSkeletal Radiology
Volume32
Issue number4
DOIs
StatePublished - Apr 1 2003

Keywords

  • Adult
  • MRI
  • Radiographs
  • Radius
  • Rosai-Dorfman disease
  • Solitary lesion

ASJC Scopus subject areas

  • Radiology Nuclear Medicine and imaging

Fingerprint Dive into the research topics of 'Rosai-Dorfman disease manifesting as a solitary lesion of the radius in a 41-year-old woman'. Together they form a unique fingerprint.

Cite this