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苍白球内侧部双侧深部脑刺激治疗莱施-尼汉病1例取得显著临床改善:五年随访

Remarkable clinical improvement with bilateral globus pallidus internus deep brain stimulation in a case of Lesch-Nyhan disease: five-year follow-up.

作者信息

Piedimonte Fabián, Andreani Juan Carlos, Piedimonte Leandro, Micheli Federico, Graff Pablo, Bacaro Valeria

机构信息

Fundación CENIT para la Investigación en Neurociencias, Buenos Aires, Argentina; Sociedad Argentina de Neuromodulación (SANE), Buenos Aires, Argentina; Instituto de Morfología "J.J. Naón," Facultad de Medicina, Universidad de Buenos Aires (UBA), Buenos Aires, Argentina.

出版信息

Neuromodulation. 2015 Feb;18(2):118-22; discussion 122. doi: 10.1111/ner.12261. Epub 2015 Jan 21.

Abstract

OBJECTIVES

Lesch-Nyhan disease (LND) is a hereditary disorder characterized by hyperuricemia, self-mutilation, developmental retardation, and movement disorders such as spasticity and dystonia. The lack of a precise understanding of the neurological dysfunction has precluded the development of useful conservative therapies. We present our experience treating a LND patient by bilateral globus pallidus internus (GPi) deep brain stimulation (DBS) with improvement in dystonia symptoms and disappearance of self-injurious behavior.

METHODS

We present a 29-year-old patient characterized by generalized severe dystonia and self-injurious behavior, both refractory to conservative treatment. The patient underwent a GPi bilateral electrode implant for chronic stimulation. Symptoms were evaluated with the Burke-Fhan-Marsden Dystonia Rating Scale (BFMDRS) and Mean Disability Scale (MDS) preoperatively and during the five-year follow-up.

RESULTS

We observed a remarkable improvement in dystonia symptoms and complete disappearance of self-injurious behavior.

CONCLUSIONS

This case supports the hypothesis that automutilation in LND might be related to dysfunction of the basal ganglia circuits and the idea that bilateral GPi-DBS is a safe and effective treatment modality for this condition.

摘要

目的

莱施-奈恩病(LND)是一种遗传性疾病,其特征为高尿酸血症、自残行为、发育迟缓以及运动障碍,如痉挛和肌张力障碍。由于对神经功能障碍缺乏精确的了解,阻碍了有效的保守治疗方法的开发。我们介绍了通过双侧内侧苍白球(GPi)深部脑刺激(DBS)治疗一名LND患者的经验,该患者的肌张力障碍症状得到改善,自残行为消失。

方法

我们介绍了一名29岁的患者,其特征为全身性严重肌张力障碍和自残行为,这两种情况对保守治疗均无效。该患者接受了双侧GPi电极植入以进行长期刺激。术前及五年随访期间,使用伯克-法恩-马斯登肌张力障碍评定量表(BFMDRS)和平均残疾量表(MDS)对症状进行评估。

结果

我们观察到肌张力障碍症状有显著改善,自残行为完全消失。

结论

该病例支持以下假设,即LND中的自残行为可能与基底神经节回路功能障碍有关,以及双侧GPi-DBS是治疗这种疾病的一种安全有效的治疗方式这一观点。

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