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Susac综合征。一种脱髓鞘疾病的鉴别诊断。

Susac syndrome. A differential diagnosis for demyelination.

作者信息

Vattoth Surjith, Compton Christopher J, Roberson Glenn H, Vaphiades Michael S

机构信息

Department of Radiology, Neuroradiology Section, University of Alabama at Birmingham, Birmingham, AL 35249-6830, USA.

出版信息

Neurosciences (Riyadh). 2013 Jan;18(1):74-8.

Abstract

Susac syndrome is a microangiopathy of unknown origin, probably autoimmune, affecting capillaries and precapillary arterioles of the brain, retina, and inner ear. It is often misdiagnosed as acute disseminated encephalomyelitis or multiple sclerosis. We report the case of a 25-year-old male with Susac syndrome who developed the clinical triad of encephalopathy, visual and hearing problems over the course of a year. The characteristic MRI findings including central corpus callosal involvement and brain infarctions were supported by branch retinal arterial/arteriolar occlusions on fluorescein retinal angiography. Most patients with Susac syndrome will not have the complete clinical triad initially. A very high index of suspicion is required by the clinician and radiologist in patients with any component of the clinical triad so as not to misdiagnose the MRI findings for demyelination. Even if initial ophthalmologic examinations are normal, these patients should be followed up for later development of branch retinal artery occlusions.

摘要

Susac综合征是一种病因不明的微血管病,可能为自身免疫性疾病,累及脑、视网膜和内耳的毛细血管及毛细血管前小动脉。它常被误诊为急性播散性脑脊髓炎或多发性硬化症。我们报告一例25岁患Susac综合征的男性病例,该患者在一年病程中出现了脑病、视觉和听力问题的临床三联征。特征性的MRI表现包括胼胝体中部受累和脑梗死,荧光素眼底血管造影显示的视网膜分支动脉/小动脉闭塞对其有支持作用。大多数Susac综合征患者最初不会出现完整的临床三联征。临床医生和放射科医生对有临床三联征任何一项表现的患者都需要高度怀疑,以免将MRI表现误诊为脱髓鞘病变。即使初始眼科检查正常,这些患者也应进行随访,观察是否会出现视网膜分支动脉闭塞。

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