Rosai-Dorfman disease manifesting as a solitary lesion of the radius in a 41-year-old woman
Authors:
- 8 March 2003
- journal article
- case report
- Published by Springer Nature in Skeletal Radiology
- Vol. 32 (4) , 236-239
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.Keywords
This publication has 10 references indexed in Scilit:
- Treatment of sinus histiocytosis with massive lymphadenopathy (rosai‐dorfman disease): Report of a case and literature reviewAmerican Journal of Hematology, 2001
- Rosai-Dorfman Disease Presenting with Isolated Bilateral Orbital Masses: Report of Two Cases2001
- Sinus Histiocytosis (Rosai-Dorfman Disease) of the Suprasellar Region: MR Imaging Findings—A Case ReportRadiology, 1999
- Sinus histiocytosis with massive lymphadenopathy (Rosai–Dorfman disease)International Journal of Pediatric Otorhinolaryngology, 1998
- Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) presenting with skeletal lesionsSkeletal Radiology, 1998
- Sinus histiocytosis with massive lymphadenopathy. Multiple skull involvementsJournal of Korean Medical Science, 1998
- Sclerotic Lesion of the Tibia without Involvement of Lymph Nodes. Report of an Unusual Case of Rosai-Dorfman Disease*Journal of Bone and Joint Surgery, 1997
- Sinus histiocytosis with massive lymphadenopathy: MRI findings of osseous lesionsSkeletal Radiology, 1996
- Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease): review of the entity.1990
- Sinus histiocytosis with massive lymphadenopathy. A newly recognized benign clinicopathological entity.1969