Suppr超能文献

分期双侧立体定向苍白球丘脑切开术治疗患有哈勒沃登-施帕茨病儿童的危及生命的肌张力障碍

Staged bilateral stereotactic pallidothalamotomy for life-threatening dystonia in a child with Hallervorden-Spatz disease.

作者信息

Balas Istvan, Kovacs Norbert, Hollody Katalin

机构信息

Department of Neurosurgery, University of Pecs, Pecs, Hungary.

出版信息

Mov Disord. 2006 Jan;21(1):82-5. doi: 10.1002/mds.20655.

Abstract

Hallervorden-Spatz disease (HSD) is a rare disorder characterized by progressive motor dysfunction and dementia. Dystonia is the most prominent and disabling symptom, responding only to a modest extent to pharmacological therapy. At the moment, only a few cases have been reported to improve dystonia and even fewer to resolve status dystonicus for a longer period in children. The authors present the case of a 10-year-old boy who had progressive generalized dystonia, resulting in spontaneous femur fracture and life-threatening swallowing and respiratory disability. As a rescue solution, staged bilateral pallidothalamotomy was performed. Postoperatively, Burke-Fahn-Marsden Dystonia Rating Scale and Dystonia Disability Rating Scale improved (from 116 and 30 points to 41 and 18 points, respectively) and painful dystonia was resolved, which was still continuous 4 years later (47 and 20 points). Stereotactic staged bilateral pallidothalamotomy should be considered as a potential treatment in the management of life-threatening generalized dystonia related to HSD.

摘要

哈勒沃登-施帕茨病(HSD)是一种罕见的疾病,其特征为进行性运动功能障碍和痴呆。肌张力障碍是最突出且致残的症状,药物治疗对此仅有一定程度的反应。目前,仅有少数儿童病例报告显示肌张力障碍有所改善,而能长期缓解肌张力障碍状态的病例更少。作者介绍了一名10岁男孩的病例,该男孩患有进行性全身性肌张力障碍,导致自发性股骨骨折以及危及生命的吞咽和呼吸功能障碍。作为一种挽救措施,实施了分期双侧苍白球丘脑切开术。术后,伯克-法恩-马斯登肌张力障碍评定量表和肌张力障碍残疾评定量表有所改善(分别从116分和30分降至41分和18分),疼痛性肌张力障碍得到缓解,4年后仍持续改善(47分和20分)。立体定向分期双侧苍白球丘脑切开术应被视为治疗与HSD相关的危及生命的全身性肌张力障碍的一种潜在方法。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验