Leucine-Rich Glioma-Inactivated 1 Encephalitis: Broadening the Sphere

IF 2.5 Q2 CLINICAL NEUROLOGY Tremor and Other Hyperkinetic Movements Pub Date : 2019-10-09 DOI:10.7916/tohm.v0.663
A. Rachdi, J. Dupouy, M. Benaiteau, C. Bost, M. Moreau, C. B. Courbon, O. Rascol, F. Magne
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引用次数: 4

Abstract

Background Leucine-rich glioma-inactivated 1 (LGI1) encephalitis is a rare entity. Its typical features are seizures, faciobrachial dystonic seizures (FBDS), cognitive impairment, and personality changes. Case report We report the case of a 66-year-old man with an unusual presentation, consisting of two types of FBDS, one starting in the foot and the other consisting of asynchronous myoclonic and dystonic jerks of the face triggered by noise and chin stimulation. The patient displayed no personality changes or cognitive impairment. Discussion LGI1 encephalitis is a heterogeneous disease. Many different forms of FBDS may be observed, and these seizures can be the only symptom. This type of encephalitis should be suspected in presenting very frequent episodic events with dystonic features, regardless of the part of the body affected.
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富亮氨酸胶质瘤-灭活1脑炎:扩大范围
背景富含亮氨酸的胶质瘤失活1型脑炎是一种罕见的疾病。其典型特征是癫痫发作、面臂肌张力障碍性发作(FBDS)、认知障碍和性格变化。病例报告我们报告了一例66岁的男性,其表现异常,由两种类型的FBDS组成,一种始于足部,另一种由噪音和下巴刺激引发的面部异步肌阵挛和肌张力障碍性抽搐组成。患者没有表现出性格变化或认知障碍。讨论LGI1脑炎是一种异质性疾病。可以观察到许多不同形式的FBDS,这些癫痫发作可能是唯一的症状。无论身体的哪个部位受到影响,这种类型的脑炎都应该被怀疑表现出非常频繁的具有肌张力特征的发作性事件。
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来源期刊
CiteScore
4.00
自引率
4.50%
发文量
31
审稿时长
6 weeks
期刊最新文献
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