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 |
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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. |
doi_str_mv | 10.1007/s00417-004-0993-9 |
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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.</description><identifier>ISSN: 0721-832X</identifier><identifier>EISSN: 1435-702X</identifier><identifier>DOI: 10.1007/s00417-004-0993-9</identifier><identifier>PMID: 15806376</identifier><language>eng</language><publisher>Germany: Springer Nature B.V</publisher><subject>Female ; Granuloma - etiology ; Histiocytosis, Sinus - complications ; Histiocytosis, Sinus - pathology ; Humans ; Middle Aged ; Skin Diseases - complications ; Skin Diseases - pathology ; Uveal Diseases - etiology ; Uveitis, Anterior - etiology</subject><ispartof>Graefe's archive for clinical and experimental ophthalmology, 2005-03, Vol.243 (3), p.281-284</ispartof><rights>Springer-Verlag 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c326t-d3cbcc32054b9431ac3724d03364c733bd058a04ee182d38036a5a79c13cb9433</citedby><cites>FETCH-LOGICAL-c326t-d3cbcc32054b9431ac3724d03364c733bd058a04ee182d38036a5a79c13cb9433</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15806376$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gaviria, Juan G</creatorcontrib><creatorcontrib>Johnson, Daniel A</creatorcontrib><creatorcontrib>Kinney, Marsha C</creatorcontrib><creatorcontrib>Proffer, Liana H</creatorcontrib><creatorcontrib>Losi-Sasaki, Jacqueline M</creatorcontrib><creatorcontrib>Kraus, Eric W</creatorcontrib><title>Bilateral anterior granulomatous uveitis associated with cutaneous Rosai-Dorfman disease</title><title>Graefe's archive for clinical and experimental ophthalmology</title><addtitle>Graefes Arch Clin Exp Ophthalmol</addtitle><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.</description><subject>Female</subject><subject>Granuloma - etiology</subject><subject>Histiocytosis, Sinus - complications</subject><subject>Histiocytosis, Sinus - pathology</subject><subject>Humans</subject><subject>Middle Aged</subject><subject>Skin Diseases - complications</subject><subject>Skin Diseases - pathology</subject><subject>Uveal Diseases - etiology</subject><subject>Uveitis, Anterior - etiology</subject><issn>0721-832X</issn><issn>1435-702X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNpdkE9LxDAUxIMo7rr6AbxI8eAt-tLXNs1R17-wIIjC3kKaZjVL26xJq_jtzdIFwcubd_jNMAwhpwwuGQC_CgAZ4zReCkIgFXtkyjLMKYd0uU-mwFNGS0yXE3IUwhoiiDk7JBOWl1AgL6ZkeWMb1RuvmkR1Ua3zybtX3dC4VvVuCMnwZWxvQ6JCcNpGtk6-bf-R6KFXndkSLy4oS2-dX7WqS2objArmmBysVBPMyU5n5O3-7nX-SBfPD0_z6wXVmBY9rVFXOr6QZ5XIkCmNPM1qQCwyzRGrGvJSQWYMK9MaS8BC5YoLzaIxGnBGLsbcjXefgwm9bG3QpmnGcrLgHBiUPILn_8C1G3wXu8kUgXMBoogQGyHtXQjerOTG21b5H8lAbjeX4-YyXrndXIroOdsFD1Vr6j_HbmT8BSEefPc</recordid><startdate>200503</startdate><enddate>200503</enddate><creator>Gaviria, Juan G</creator><creator>Johnson, Daniel A</creator><creator>Kinney, Marsha C</creator><creator>Proffer, Liana H</creator><creator>Losi-Sasaki, Jacqueline M</creator><creator>Kraus, Eric W</creator><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>200503</creationdate><title>Bilateral anterior granulomatous uveitis associated with cutaneous Rosai-Dorfman disease</title><author>Gaviria, Juan G ; Johnson, Daniel A ; Kinney, Marsha C ; Proffer, Liana H ; Losi-Sasaki, Jacqueline M ; Kraus, Eric W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c326t-d3cbcc32054b9431ac3724d03364c733bd058a04ee182d38036a5a79c13cb9433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Female</topic><topic>Granuloma - etiology</topic><topic>Histiocytosis, Sinus - complications</topic><topic>Histiocytosis, Sinus - pathology</topic><topic>Humans</topic><topic>Middle Aged</topic><topic>Skin Diseases - complications</topic><topic>Skin Diseases - pathology</topic><topic>Uveal Diseases - etiology</topic><topic>Uveitis, Anterior - etiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gaviria, Juan G</creatorcontrib><creatorcontrib>Johnson, Daniel A</creatorcontrib><creatorcontrib>Kinney, Marsha C</creatorcontrib><creatorcontrib>Proffer, Liana H</creatorcontrib><creatorcontrib>Losi-Sasaki, Jacqueline M</creatorcontrib><creatorcontrib>Kraus, Eric W</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Graefe's archive for clinical and experimental ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gaviria, Juan G</au><au>Johnson, Daniel A</au><au>Kinney, Marsha C</au><au>Proffer, Liana H</au><au>Losi-Sasaki, Jacqueline M</au><au>Kraus, Eric W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bilateral anterior granulomatous uveitis associated with cutaneous Rosai-Dorfman disease</atitle><jtitle>Graefe's archive for clinical and experimental ophthalmology</jtitle><addtitle>Graefes Arch Clin Exp Ophthalmol</addtitle><date>2005-03</date><risdate>2005</risdate><volume>243</volume><issue>3</issue><spage>281</spage><epage>284</epage><pages>281-284</pages><issn>0721-832X</issn><eissn>1435-702X</eissn><abstract>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.</abstract><cop>Germany</cop><pub>Springer Nature B.V</pub><pmid>15806376</pmid><doi>10.1007/s00417-004-0993-9</doi><tpages>4</tpages></addata></record> |
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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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