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偏侧肌张力障碍:22例患者的报告及文献综述

Hemidystonia: a report of 22 patients and a review of the literature.

作者信息

Pettigrew L C, Jankovic J

出版信息

J Neurol Neurosurg Psychiatry. 1985 Jul;48(7):650-7. doi: 10.1136/jnnp.48.7.650.

Abstract

Hemidystonia defined as involuntary, sustained posturing of the unilateral arm, leg, and face was studied in 12 male and 10 female patients. Hemidystonia was caused by cerebrovascular disease in eight patients, perinatal trauma or childhood injury in four, head trauma and its sequelae in three, neuronal storage disorders in two, neurodegenerative disease in two, lesions after thalamotomy in two, and presumed encephalitis in one. Sixteen patients (73%) had CT evidence of contralateral basal ganglia damage, history of hemiparesis, or both. Brain damage before 7 years of age produced contralateral hemidystonia with a mean delay of 9-7 years. In older patients hemidystonia appeared within 6 months after injury. Hemidystonia may result from a disconnection between the striatum and the thalamus with relative preservation of the corticospinal pathways.

摘要

对12例男性和10例女性患者进行了半身肌张力障碍的研究,半身肌张力障碍定义为单侧手臂、腿部和面部的不自主持续性姿势。8例患者的半身肌张力障碍由脑血管疾病引起,4例由围产期创伤或儿童期损伤引起,3例由头部创伤及其后遗症引起,2例由神经元贮积症引起,2例由神经退行性疾病引起,2例由丘脑切开术后病变引起,1例由推测的脑炎引起。16例患者(73%)有对侧基底节损害的CT证据、偏瘫病史或两者皆有。7岁前的脑损伤导致对侧半身肌张力障碍,平均延迟9至7年。在老年患者中,半身肌张力障碍在受伤后6个月内出现。半身肌张力障碍可能是由于纹状体与丘脑之间的联系中断,而皮质脊髓通路相对保留所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c80/1028406/3d4681900885/jnnpsyc00111-0041-a.jpg

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