Suppr超能文献

马尾受累于苏萨克综合征。

Cauda equina involvement in Susac's syndrome.

作者信息

Allmendinger Andrew M, Mallery Robert M, Magro Cynthia M, Wang Nancy, Egan Robert A, Samuels Martin A, Callahan Alison, Viswanadhan Narayan, Klufas Roman A, Hsu Liangge, Prasad Sashank

机构信息

Department of Radiology, Brigham and Women's Hospital, Boston, MA, United States.

Departments of Neurology and Ophthalmology, University of Pennsylvania, Philadelphia, PA, United States.

出版信息

J Neurol Sci. 2014 Feb 15;337(1-2):91-6. doi: 10.1016/j.jns.2013.11.023. Epub 2013 Nov 22.

Abstract

Susac's syndrome is a rare autoimmune microangiopathy characterized by the clinical triad of encephalopathy, branch retinal artery occlusions, and sensorineural hearing loss. In many cases, the clinical triad is not fully present at the onset of symptoms. MRI studies often show characteristic punched out lesions of the central fibers of the corpus callosum, and leptomeningeal enhancement and deep gray matter lesions may also be seen. Here we present a case of Susac's syndrome in a middle aged man with the unique clinical finding of cauda equina syndrome and spinal MRI showing diffuse lumbosacral nerve root enhancement. Biopsy specimens of the brain, leptomeninges, and skin showed evidence of a pauci-immune endotheliopathy, consistent with pathology described in previous cases of Susac's syndrome. This case is important not only because it expands the clinical features of Susac's syndrome but also because it clarifies the mechanism of a disorder of the endothelium, an important target for many disorders of the nervous system.

摘要

苏萨克综合征是一种罕见的自身免疫性微血管病,其特征为脑病、视网膜分支动脉阻塞和感音神经性听力损失组成的临床三联征。在许多病例中,症状发作时临床三联征并不完全具备。MRI研究常显示胼胝体中央纤维有特征性的筛孔状病变,也可见软脑膜强化和深部灰质病变。在此,我们报告一例中年男性苏萨克综合征病例,其独特的临床表现为马尾综合征,脊柱MRI显示腰骶神经根弥漫性强化。脑、软脑膜和皮肤活检标本显示为寡免疫性内皮病,与既往苏萨克综合征病例所描述的病理情况相符。该病例之所以重要,不仅在于它扩展了苏萨克综合征的临床特征,还在于它阐明了内皮功能障碍的机制,而内皮是许多神经系统疾病的重要靶点。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验