Orbital Rosai-Dorfman Disease in a fifty-eight years old woman.

Abstract:

:Rosai-Dorfman disease (RDD) is rare and characterized by histiocytic proliferation and massive cervical lymphadenopathy. About 40% of patients have extra-nodal involvement. Opthalmic involvement is seen in 10% of cases. A case of orbital Rosai Dorfman disease in a 58 years old woman is presented here, who was misdiagnosed as orbital inflammatory disease initially. The patient did not respond to a course of oral prednisolone. Then complete surgical excision of the mass was performed and the histopathological examination was consistent with a diagnosis of RDD.

journal_name

Pak J Med Sci

authors

Li HY,Cui HG,Zheng XY,Ren GP,Gu YS

doi

10.12669/pjms.294.3554

subject

Has Abstract

pub_date

2013-07-01 00:00:00

pages

1065-7

issue

4

eissn

1682-024X

issn

1681-715X

journal_volume

29

pub_type

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