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[一例表现为震颤的皮质反射性肌阵挛病例]

[A case of cortical reflex myoclonus manifesting tremor].

作者信息

Takigawa T, Mima T, Saida K, Kawasaki J, Shibasaki H

机构信息

Department of Neurology and Psychiatry, Utano National Hospital.

出版信息

Rinsho Shinkeigaku. 1997 Nov;37(11):1006-9.

PMID:9503972
Abstract

A 58-year-old woman developed slowly progressive tremulous myoclonus provoked mainly by action and posture. She had neither seizure nor dementia. No one in her family had similar symptoms. The presence of giant somatosensory evoked potentials (SEP) with enhanced long loop reflex and premovement cortical spikes demonstrated by the jerk-locked averaging method suggest that the involuntary movement is cortical reflex myoclonus. Magnetoencephalogram revealed that the generator sources of giant SEPs were the post-central somatosensory cortex and probably also the pre-central motor cortex. Symptoms improved after treatment with zonisamide, clonazepam and valpolate. This kind of involuntary movement might be called cortical myoclonic tremor.

摘要

一名58岁女性出现主要由动作和姿势诱发的缓慢进展性震颤性肌阵挛。她既无癫痫发作也无痴呆。其家族中无人有类似症状。通过抽搐锁定平均法显示存在巨大体感诱发电位(SEP)、长环反射增强以及运动前皮质棘波,提示这种不自主运动为皮质反射性肌阵挛。脑磁图显示巨大SEP的发生器来源为中央后体感皮层,可能还包括中央前运动皮层。使用唑尼沙胺、氯硝西泮和丙戊酸盐治疗后症状改善。这种不自主运动可能被称为皮质性肌阵挛性震颤。

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