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迟发性运动障碍作为桥脑中央髓鞘溶解症的一种并发症。

Delayed onset movement disorders as a complication of central pontine myelinolysis.

作者信息

Tison F X, Ferrer X, Julien J

机构信息

Department of Neurology, Hôpital du Haut Lévêque, Pessac, France.

出版信息

Mov Disord. 1991;6(2):171-3. doi: 10.1002/mds.870060215.

DOI:10.1002/mds.870060215
PMID:2057010
Abstract

This report describes a case of central pontine myelinolysis occurring after a rapid correction of profound hyponatremia. Delayed-onset generalized dystonia and choreoathetosis then appeared. A small pontine myelinolysis was demonstrated by magnetic resonance images, but striatal myelinolysis could not be established. Aspects of movement disorders associated with the osmotic demyelination syndrome are briefly reviewed and discussed.

摘要

本报告描述了一例在严重低钠血症快速纠正后发生的中央桥脑髓鞘溶解症。随后出现迟发性全身性肌张力障碍和舞蹈指划样动作。磁共振成像显示有一小片桥脑髓鞘溶解,但纹状体髓鞘溶解无法确诊。本文简要回顾并讨论了与渗透性脱髓鞘综合征相关的运动障碍方面的问题。

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Dystonia in central pontine myelinolysis without evidence of extrapontine myelinolysis.中央桥脑髓鞘溶解症中的肌张力障碍,无桥脑外髓鞘溶解症证据。
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