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X 连锁型肌张力障碍帕金森病的深部脑刺激治疗前景。

The promise of deep brain stimulation in X-linked dystonia parkinsonism.

机构信息

Philippine Movement Disorder Surgery Center, Cardinal Santos Medical Center, Wilson St., MetroManila, Philippines.

出版信息

Int J Neurosci. 2011;121 Suppl 1:57-63. doi: 10.3109/00207454.2010.541573. Epub 2011 Jan 19.

Abstract

X-Linked dystonia parkinsonism (XDP) is a rapidly progressive and disabling neurodegenerative disease affecting mainly male Filipinos with origins from Panay Island. We reviewed all the past neurosurgical ablative procedures done for XDP patients listed in the Philippine XDP registry. From 1960 to 1982, six patients had undergone bilateral chemopallidotomies or bilateral thalomotomies staged over time. Half of these patients had significant improvement in their symptoms but five of the six patients (83%) developed postoperative morbidities, mainly speech impairment or hemiparesis. All the five reported GPi deep brain stimulation (DBS) cases for XDP were also reviewed, showing consistently immediate improvement of symptoms (61.5%-88.3% decrease in the Burke-Marsden-Fahn Dystonia Rating Scale) lasting up to a year with no adverse effects noted. We also present the first Philippine case of GPi DBS done in the youngest XDP patient to date. This present case showed dramatic improvement (88.3% decrease of the Burke-Marsden-Fahn Dystonia Rating Scale) of his dystonic symptoms, without incurring any persistent adverse effects. The results of these early cases of pallidal DBS for XDP show that DBS is generally a safe and effective procedure for alleviating the disabling symptoms of XDP in contrast to previous ablative surgeries performed on these patients.

摘要

X 连锁肌张力障碍性帕金森病(XDP)是一种进行性和致残性神经退行性疾病,主要影响来自菲律宾帕奈岛的菲律宾男性。我们回顾了菲律宾 XDP 登记处列出的所有过去用于 XDP 患者的神经外科消融手术。从 1960 年到 1982 年,六名患者接受了分期双侧苍白球切开术或双侧丘脑切开术。这些患者中有一半的症状有明显改善,但六名患者中的五名(83%)出现了术后并发症,主要是言语障碍或偏瘫。还回顾了所有五例报告的 XDP 的 GPi 深部脑刺激(DBS)病例,均显示出一致的即刻症状改善(Burke-Marsden-Fahn 肌张力障碍评定量表减少 61.5%-88.3%),持续长达一年,且无不良反应。我们还介绍了菲律宾首例迄今为止最年轻的 XDP 患者的 GPi DBS 病例。该病例的肌张力障碍症状明显改善(Burke-Marsden-Fahn 肌张力障碍评定量表减少 88.3%),且没有发生任何持续的不良反应。这些 XDP 患者的早期苍白球 DBS 结果表明,与之前对这些患者进行的消融手术相比,DBS 通常是一种安全有效的缓解 XDP 致残症状的方法。

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