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表现为孤立性自发性发作性构音障碍的孤立性硬化症。

Solitary sclerosis presenting as isolated spontaneous paroxysmal dysarthria.

作者信息

Xia Yuanxuan, Shoemaker Thomas, Gorelick Noah, McArthur Justin C

机构信息

Department of Neurology, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.

出版信息

eNeurologicalSci. 2019 Jan 11;14:98-100. doi: 10.1016/j.ensci.2019.01.001. eCollection 2019 Mar.

Abstract

Paroxysmal dysarthria and ataxia (PDA) is a rare syndrome characterized by brief, stereotyped episodes of slurred speech, clumsiness with extremities, or vertigo. It is usually observed in young patients suffering from multiple sclerosis with numerous lesions. PDA is challenging to identify in those presenting with atypical patterns. Here, a non-ataxic variant of PDA in an otherwise neurologically healthy elderly man is presented who had a single midbrain lesion. A broad diagnostic workup illustrates the challenges of identifying PDA. Teaching points emphasize the significance of the midbrain lesion and response to anti-epileptic medication.

摘要

阵发性构音障碍和共济失调(PDA)是一种罕见综合征,其特征为言语含糊、肢体笨拙或眩晕的短暂、刻板发作。它通常见于患有多发性硬化且有大量病灶的年轻患者。对于表现出非典型模式的患者,识别PDA具有挑战性。在此,报告了一名无共济失调变异型PDA的老年男性,其神经系统其他方面健康,仅有一个中脑病灶。全面的诊断检查说明了识别PDA的挑战。教学要点强调了中脑病灶的重要性以及对抗癫痫药物的反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74c6/6382995/a7a3829b11bf/gr1.jpg

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