Bilateral anterior granulomatous uveitis associated with cutaneous Rosai-Dorfman disease

Juan G. Gaviria; Daniel A. Johnson; Marsha C. Kinney; Liana H. Proffer; Jacqueline M. Losi-Sasaki; Eric W. Kraus

doi:10.1007/s00417-004-0993-9

Bilateral anterior granulomatous uveitis associated with cutaneous Rosai-Dorfman disease

Juan G. Gaviria
, Daniel A. Johnson
, Marsha C. Kinney
, Liana H. Proffer
, Jacqueline M. Losi-Sasaki
, Eric W. Kraus

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

12 Scopus citations

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. 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. Results: On the basis of skin biopsy, purely cutaneous RDD was established. Conclusion: Anterior granulomatous uveitis may be the presenting sign of cutaneous RDD. Consultation is necessary for accurate diagnosis.

Original language	English (US)
Pages (from-to)	281-284
Number of pages	4
Journal	Graefe's Archive for Clinical and Experimental Ophthalmology
Volume	243
Issue number	3
DOIs	https://doi.org/10.1007/s00417-004-0993-9
State	Published - Mar 2005

ASJC Scopus subject areas

Sensory Systems
Cellular and Molecular Neuroscience
Ophthalmology

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10.1007/s00417-004-0993-9

Cite this

@article{b955c5d9e39e4e90bb3592d600386846,

title = "Bilateral anterior granulomatous uveitis associated with cutaneous Rosai-Dorfman disease",

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. 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. Results: On the basis of skin biopsy, purely cutaneous RDD was established. Conclusion: Anterior granulomatous uveitis may be the presenting sign of cutaneous RDD. Consultation is necessary for accurate diagnosis.",

author = "Gaviria, \{Juan G.\} and Johnson, \{Daniel A.\} and Kinney, \{Marsha C.\} and Proffer, \{Liana H.\} and Losi-Sasaki, \{Jacqueline M.\} and Kraus, \{Eric W.\}",

note = "Funding Information: Acknowledgement This work was supported in part by Research to Prevent Blindness, New York, NY.",

year = "2005",

month = mar,

doi = "10.1007/s00417-004-0993-9",

language = "English (US)",

volume = "243",

pages = "281--284",

journal = "Graefe's Archive for Clinical and Experimental Ophthalmology",

issn = "0721-832X",

publisher = "Springer Verlag",

number = "3",

}

TY - JOUR

T1 - Bilateral anterior granulomatous uveitis associated with cutaneous Rosai-Dorfman disease

AU - Gaviria, Juan G.

AU - Johnson, Daniel A.

AU - Kinney, Marsha C.

AU - Proffer, Liana H.

AU - Losi-Sasaki, Jacqueline M.

AU - Kraus, Eric W.

N1 - Funding Information: Acknowledgement This work was supported in part by Research to Prevent Blindness, New York, NY.

PY - 2005/3

Y1 - 2005/3

N2 - 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. 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. Results: On the basis of skin biopsy, purely cutaneous RDD was established. Conclusion: Anterior granulomatous uveitis may be the presenting sign of cutaneous RDD. Consultation is necessary for accurate diagnosis.

AB - 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. 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. Results: On the basis of skin biopsy, purely cutaneous RDD was established. Conclusion: Anterior granulomatous uveitis may be the presenting sign of cutaneous RDD. Consultation is necessary for accurate diagnosis.

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U2 - 10.1007/s00417-004-0993-9

DO - 10.1007/s00417-004-0993-9

M3 - Article

C2 - 15806376

AN - SCOPUS:17144365086

SN - 0721-832X

VL - 243

SP - 281

EP - 284

JO - Graefe's Archive for Clinical and Experimental Ophthalmology

JF - Graefe's Archive for Clinical and Experimental Ophthalmology

IS - 3

ER -

Bilateral anterior granulomatous uveitis associated with cutaneous Rosai-Dorfman disease

Abstract

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