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Bilateral anterior granulomatous uveitis associated with cutaneous Rosai-Dorfman disease.

Authors :
Gaviria JG
Johnson DA
Kinney MC
Proffer LH
Losi-Sasaki JM
Kraus EW
Source :
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie [Graefes Arch Clin Exp Ophthalmol] 2005 Mar; Vol. 243 (3), pp. 281-4. Date of Electronic Publication: 2004 Sep 30.
Publication Year :
2005

Abstract

Background: Rosai-Dorfman disease (RDD) is a benign, rare, histiocytic disorder of unknown etiology. We describe the case of a 61-year-old woman who presented to the ophthalmology clinic with bilateral granulomatous anterior uveitis.<br />Methods: The uveitis was controlled on topical prednisolone acetate 1%. One month after presentation, she developed generalized macules and papules, and dermatologic and systemic evaluations were performed.<br />Results: On the basis of skin biopsy, purely cutaneous RDD was established.<br />Conclusion: Anterior granulomatous uveitis may be the presenting sign of cutaneous RDD. Consultation is necessary for accurate diagnosis.

Details

Language :
English
ISSN :
0721-832X
Volume :
243
Issue :
3
Database :
MEDLINE
Journal :
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie
Publication Type :
Academic Journal
Accession number :
15806376
Full Text :
https://doi.org/10.1007/s00417-004-0993-9