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多发性硬化症患者中的伏格特-小柳-原田综合征

Vogt-Koyanagi-Harada syndrome in a case of multiple sclerosis.

作者信息

Montero Javier A, Sanchis M Eugenia, Fernandez-Munoz Marta

机构信息

VISSUM, Instituto Oftalmológico de Alicante, Retina Unit, Alicante, Spain.

出版信息

J Neuroophthalmol. 2007 Mar;27(1):36-40. doi: 10.1097/WNO.0b013e3180325d84.

Abstract

A 34-year-old woman in whom multiple sclerosis (MS) had been diagnosed 2 years earlier developed progressive bilateral visual loss associated with peripapillary exudative retinal detachment and other features of Vogt-Koyanagi-Harada (VKH) syndrome. She was treated with corticosteroid pulses and interferon beta-1A with visual acuity improvement and resolution of the retinal detachment. This is the first reported case of VKH syndrome in a patient with MS. The combination of VKH syndrome and MS suggests a common autoimmune pathogenesis.

摘要

一名34岁女性,两年前被诊断为多发性硬化症(MS),现出现进行性双侧视力丧失,伴有视乳头周围渗出性视网膜脱离及Vogt-小柳-原田(VKH)综合征的其他特征。她接受了糖皮质激素冲击治疗和干扰素β-1A治疗,视力得到改善,视网膜脱离也得以消退。这是首例报道的MS患者并发VKH综合征的病例。VKH综合征与MS并存提示存在共同的自身免疫发病机制。

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