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首页> 外文期刊>Stereotactic and Functional Neurosurgery: Official Journal of the World Society for Stereotactic and Functional Neurosurgery >Unilateral pallidal deep brain stimulation in a patient with dystonia secondary to episodic ataxia type 2
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Unilateral pallidal deep brain stimulation in a patient with dystonia secondary to episodic ataxia type 2

机译:发作性共济失调2型继发性肌张力障碍患者的单侧苍白球深脑刺激

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摘要

Background/Aims: This paper describes the use of deep brain stimulation (DBS) of the globus pallidus internus (GPi) in the treatment of secondary dystonia caused by expisodic ataxia type 2 (EA2). Methods: We present the case of a patient with EA2, an autosomal dominant condition, who developed late-onset cervical and right upper limb segmental dystonia. The patient underwent left GPi DBS. Results: Within 4 months of commencing stimulation of the left GPi, the patient had resolution of his neck pain and was able to keep the head straighter for longer time intervals. There was also improvement in right arm segmental dystonia. There was an improvement in the Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS 21.5) of 55% at 4 months and of 51% at 22 months. Conclusion: The treatment of secondary dystonia is difficult and the results with GPi DBS are less favourable compared with primary dystonia. This case illustrates the successful treatment of secondary dystonia caused by EA2.
机译:背景/目的:本文介绍了苍白苍白球内侧脑(GPi)的深部脑刺激(DBS)在治疗由2型间歇性共济失调(EA2)引起的继发性肌张力障碍中的用途。方法:我们介绍了一名常染色体显性遗传疾病EA2患者,该患者发展为迟发性宫颈和右上肢节段性肌张力障碍。患者接受了左GPi DBS治疗。结果:开始刺激左GPi后的4个月内,患者的颈部疼痛得以缓解,并且能够在更长的时间间隔内保持头部挺直。右臂节段性肌张力障碍也有所改善。多伦多西部痉挛性斜颈评分量表(TWSTRS 21.5)在4个月时改善了55%,在22个月时改善了51%。结论:与原发性肌张力障碍相比,继发性肌张力障碍的治疗困难,GPi DBS的效果较差。该病例说明了由EA2引起的继发性肌张力障碍的成功治疗。

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