Bilateral anterior granulomatous uveitis associated with cutaneous Rosai-Dorfman disease

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. The uveitis was controlled on topical prednisolone acetate 1%. One month after...

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Veröffentlicht in:Graefe's archive for clinical and experimental ophthalmology 2005-03, Vol.243 (3), p.281-284
Hauptverfasser: Gaviria, Juan G, Johnson, Daniel A, Kinney, Marsha C, Proffer, Liana H, Losi-Sasaki, Jacqueline M, Kraus, Eric W
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container_title Graefe's archive for clinical and experimental ophthalmology
container_volume 243
creator Gaviria, Juan G
Johnson, Daniel A
Kinney, Marsha C
Proffer, Liana H
Losi-Sasaki, Jacqueline M
Kraus, Eric W
description 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. 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. On the basis of skin biopsy, purely cutaneous RDD was established. Anterior granulomatous uveitis may be the presenting sign of cutaneous RDD. Consultation is necessary for accurate diagnosis.
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subjects Female
Granuloma - etiology
Histiocytosis, Sinus - complications
Histiocytosis, Sinus - pathology
Humans
Middle Aged
Skin Diseases - complications
Skin Diseases - pathology
Uveal Diseases - etiology
Uveitis, Anterior - etiology
title Bilateral anterior granulomatous uveitis associated with cutaneous Rosai-Dorfman disease
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