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双侧内囊梗死所致急性起病的持续性缄默症和吞咽困难。

Persistent mutism and dysphagia of acute onset due to bilateral internal capsule infarction.

作者信息

Chee M W, Tan C B, Tjia H T

机构信息

Department of Neurology, Tan Tock Seng Hospital, Singapore.

出版信息

Ann Acad Med Singap. 1990 May;19(3):393-5.

PMID:2393243
Abstract

Acute mutism with paralysis of the bulbar and facial muscles following discrete bilateral internal capsular infarction is a rare stroke syndrome. We describe a 62 year-old male who suddenly became unable to speak or swallow. The paucity of facial expression and inability to voluntarily move the facial, lingual and pharyngeal muscles were persistent and contrasted with a relatively mild limb paresis which recovered. High resolution CT scan revealed infarcts in the posterior limbs of both internal capsules. It is important to recognise this stroke syndrome because of the permanence of dysarthria and dysphagia associated with it.

摘要

双侧内囊梗死灶散在分布后出现急性缄默症伴延髓和面部肌肉麻痹是一种罕见的中风综合征。我们描述了一名62岁男性,他突然无法说话或吞咽。面部表情缺乏以及无法自主活动面部、舌部和咽部肌肉的情况持续存在,与之形成对比的是相对较轻的肢体轻瘫,后者已恢复。高分辨率CT扫描显示双侧内囊后肢梗死。认识到这种中风综合征很重要,因为与之相关的构音障碍和吞咽困难是永久性的。

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