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

doi:10.1007/s00256-002-0613-x

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

Orthopaedic Surgery

Research output: Contribution to journal › Article › peer-review

26 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 language	English (US)
Pages (from-to)	236-239
Number of pages	4
Journal	Skeletal Radiology
Volume	32
Issue number	4
DOIs	https://doi.org/10.1007/s00256-002-0613-x
State	Published - Apr 1 2003

Keywords

Adult
MRI
Radiographs
Radius
Rosai-Dorfman disease
Solitary lesion

ASJC Scopus subject areas

Radiology Nuclear Medicine and imaging

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1007/s00256-002-0613-x

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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.",

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AU - George, J.

AU - Stacy, G.

AU - Peabody, T.

AU - Montag, A.

PY - 2003/4/1

Y1 - 2003/4/1

N2 - 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.

AB - 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.

KW - Adult

KW - MRI

KW - Radiographs

KW - Radius

KW - Rosai-Dorfman disease

KW - Solitary lesion

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ER -

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

Abstract

Keywords

ASJC Scopus subject areas

UN SDGs

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