Ocular manifestations in systemic lupus erythematosus

被引:143
作者
Silpa-archa, Sukhum [1 ,2 ,3 ]
Lee, Joan J. [1 ,2 ]
Foster, C. Stephen [1 ,2 ,4 ]
机构
[1] Massachusetts Eye Res & Surg Inst, Cambridge, MA 02142 USA
[2] Ocular Immunol & Uveitis Fdn, Cambridge, MA USA
[3] Rangsit Univ, Coll Med, Rajavithi Hosp, Fac Med,Dept Ophthalmol, Bangkok, Thailand
[4] Harvard Univ, Sch Med, Boston, MA USA
关键词
ENDOTHELIAL GROWTH-FACTOR; SEVERE VASOOCCLUSIVE RETINOPATHY; OPTIC NEUROPATHY; ORBITAL MYOSITIS; INTRAVITREAL BEVACIZUMAB; PSEUDOTUMOR CEREBRI; RETINAL VASCULITIS; VEIN OCCLUSION; FOLLOW-UP; CHOROIDOPATHY;
D O I
10.1136/bjophthalmol-2015-306629
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Systemic lupus erythematosus (SLE) can involve many parts of the eye, including the eyelid, ocular adnexa, sclera, cornea, uvea, retina and optic nerve. Ocular manifestations of SLE are common and may lead to permanent blindness from the underlying disease or therapeutic side effects. Keratoconjunctivitis sicca is the most common manifestation. However, vision loss may result from involvement of the retina, choroid and optic nerve. Ocular symptoms are correlated to systemic disease activity and can present as an initial manifestation of SLE. The established treatment includes prompt systemic corticosteroids, steroid-sparing immunosuppressive drugs and biological agents. Local ocular therapies are options with promising efficacy. The early recognition of disease and treatment provides reduction of visual morbidity and mortality.
引用
收藏
页码:135 / 141
页数:7
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