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不要忘记不明原因急性意识混乱患者的 Susac 综合征。

Do not forget Susac syndrome in patients with unexplained acute confusion.

机构信息

Department of Neurology, Loyola University Chicago Stritch School of Medicine, Maywood, Illinois.

Department of Neurology, Loyola University Chicago Stritch School of Medicine, Maywood, Illinois.

出版信息

J Stroke Cerebrovasc Dis. 2015 Apr;24(4):e93-5. doi: 10.1016/j.jstrokecerebrovasdis.2014.11.028. Epub 2015 Feb 11.

Abstract

BACKGROUND

To report 2 patients with Susac syndrome presenting with acute confusion and abnormal neuroimaging and cerebrospinal fluid (CSF) findings, both of whom were initially misdiagnosed. Susac syndrome is a rare, though likely underdiagnosed, endotheliopathy defined clinically by the triad of encephalopathy, branch retinal artery occlusions (BRAOs), and sensorineural hearing loss (SNHL). Its pathogenesis remains poorly understood. The classic clinical triad may not be fully developed at initial presentation, even at the time magnetic resonance imaging (MRI) demonstrates characteristic central corpus callosum lesions.

METHODS

We describe the patient's clinical course, investigations, management, and follow-up.

RESULTS

A 57-year-old woman had acute onset of confusion and was initially thought to have multiple strokes. MRI demonstrated restricted diffusion involving the splenium of the corpus callosum and CSF showed elevated protein levels. Audiometry showed asymmetric bilateral SNHL. Fluorescein angiography showed multiple bilateral BRAOs. Patient received corticosteroids and intravenous immunoglobulin (IVIG). At 1-month follow-up, patient's confusion had resolved. The second patient was a 32-year-old man who had acute onset of confusion. CSF demonstrated pleocytosis and elevated protein. MRI demonstrated restricted diffusion involving the corpus callosum. Patient was discharged and rehospitalized 20 days later where he was diagnosed with acute disseminated encephalomyelitis. Patient presented a third time with vision loss. Fluorescein angiography demonstrated bilateral BRAOs. Audiometry noted bilateral SNHL. He received IVIG and discharged on a prednisone taper and mycophenolate mofetil. At 1-month follow-up, patient's confusion had resolved.

CONCLUSIONS

We report 2 patients evaluated within 1 month of each other who presented with acute confusion and were eventually diagnosed with Susac syndrome. Susac syndrome should be considered in young patients with otherwise unexplained acute onset of confusion with MRI and CSF changes as described previously.

摘要

背景

报告 2 例以急性意识混乱和异常神经影像学及脑脊液(CSF)表现为特征的 Susac 综合征患者,均最初误诊。Susac 综合征是一种罕见但可能被低估的内皮病,临床上定义为脑病、视网膜分支动脉阻塞(BRAO)和感觉神经性听力损失(SNHL)三联征。其发病机制仍不清楚。即使磁共振成像(MRI)显示典型的胼胝体中央体病变,经典的临床三联征也可能在初始表现时未完全出现。

方法

我们描述了患者的临床病程、检查、治疗和随访情况。

结果

一位 57 岁女性突发意识混乱,最初被认为是多发性中风。MRI 显示胼胝体压部弥散受限,CSF 蛋白水平升高。听力图显示双侧非对称 SNHL。荧光素血管造影显示双侧多发 BRAO。患者接受了皮质类固醇和静脉注射免疫球蛋白(IVIG)治疗。1 个月随访时,患者的意识混乱已缓解。第二位患者是一位 32 岁男性,突发意识混乱。CSF 显示细胞增多和蛋白升高。MRI 显示胼胝体弥散受限。患者出院并在 20 天后再次住院,被诊断为急性播散性脑脊髓炎。第三次就诊时患者出现视力丧失。荧光素血管造影显示双侧 BRAO。听力图显示双侧 SNHL。他接受了 IVIG 治疗,出院时接受泼尼松减量和吗替麦考酚酯治疗。1 个月随访时,患者的意识混乱已缓解。

结论

我们报告了 2 例在彼此相隔 1 个月内接受评估的患者,他们均以急性意识混乱为首发表现,最终被诊断为 Susac 综合征。对于以MRI 和 CSF 改变为特征的不明原因的急性意识混乱年轻患者,应考虑 Susac 综合征。

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