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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/28211
Title: Uveitis in Patients with Autoimmune Hepatitis
Authors: Lyndell L. Lim
John D. Scarborough
Jennifer E. Thorne
Elizabeth Graham
John H. Kempen
Friederike Mackensen
Quan Dong Nguyen
Tisha Prabriputaloong
Russell W. Read
Eric B. Suhler
Jonathan M. Schwartz
Justine R. Smith
OHSU School of Medicine
Oregon Health and Science University
University of Melbourne
The Wilmer Eye Institute at Johns Hopkins
Guy's and St Thomas' NHS Foundation Trust
University of Pennsylvania, Health System
Universitat Heidelberg
Mahidol University
University of Alabama at Birmingham
Keywords: Medicine
Issue Date: 1-Feb-2009
Citation: American Journal of Ophthalmology. Vol.147, No.2 (2009)
Abstract: Purpose: To report seven cases of uveitis occurring in patients with autoimmune hepatitis (AIH), raising the possibility that uveitis may be an extrahepatic feature of AIH. Design: Multicenter, retrospective, observational case series of patients with AIH and uveitis. Methods: One index case was identified at Oregon Health & Science University. Further cases were identified by a web-based survey of members of the American Uveitis Society, the International Uveitis Study Group, the Proctor Foundation mailing list server, and the First SUN International Workshop. Respondents were asked to provide clinical information about uveitis phenotype, AIH features, and treatment. Results: Clinical information was obtained for seven individuals (four females and three males; age range, seven to 67 years) who suffered from AIH and uveitis. Average duration of follow-up was 5.5 years. All patients had chronic, persistent bilateral uveitis that was anterior (n = 3), intermediate (n = 1), or pan (n = 3) in location. Every patient had complications arising from his or her uveitis, including cataract (n = 5), glaucoma (n = 3), cystoid macular edema (n = 3), and posterior synechiae (n = 3). Final visual acuities ranged from 20/16 to hand movements. To treat the uveitis and/or AIH, the majority of patients required oral prednisone and all seven patients were treated with systemic immunosuppression. Conclusion: Despite the small size of this study, our findings suggest an association between AIH and uveitis. The uveitis is chronic, bilateral, and associated with sight-threatening complications, necessitating systemic immunosuppression in some individuals. © 2009 Elsevier Inc. All rights reserved.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=58249098858&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/28211
ISSN: 00029394
Appears in Collections:Scopus 2006-2010

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