Ocular manifestations and concepts of systemic vasculitides

被引:41
|
作者
Perez, VL
Chavala, SH
Ahmed, M
Chu, D
Zafirakis, P
Baltatzis, S
Ocampo, V
Foster, CS
机构
[1] Harvard Univ, Sch Med, Massachusetts Eye & Ear Infirm, Immunol & Uveitis Serv, Boston, MA 02114 USA
[2] Cleveland Clin Fdn, Cole Eye Inst, Cornea & Uveitis Serv, Cleveland, OH 44195 USA
[3] Univ Med & Dent New Jersey, Newark, NJ 07103 USA
关键词
Churg-Strauss syndrome; cutaneous leukocytoclastic angiitis; giant cell arteritis; Henoch-Schonlein purpura; Kawasaki disease; microscopic polyangiitis; ocular manifestations; polyarteritis nodosa; primary vasculitis; Takayasu's arteritis; Wegener's granulomatosis;
D O I
10.1016/j.survophthal.2004.04.008
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Vasculitic disorders are relatively rare. Their etiology and pathophysiology remain enigmatic, leading to confusing nomenclature and multiple classification schemes. Untreated vasculitis can be fatal. Early diagnosis is the key to successful treatment and better prognosis. However, early diagnosis can be difficult; vasculitic conditions usually present with non-specific symptoms for a long period before clinically overt manifestations occur. Ophthalmologists should be familiar with the ocular manifestations of the vasculitic disorders because they may not only be sight-threatening, but more importantly could be the presenting manifestations of active, potentially lethal systemic disease. This review summarizes clinical and ocular manifestations of systemic vasculitic disorders. Furthermore, it discusses general concepts in diagnosis and treatment of these diseases in an effort to provide a practical framework for the ophthalmologist evaluating patients with vasculitis. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:399 / 418
页数:20
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