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儿童扭转性肌张力障碍的脑深部电刺激治疗

Deep brain stimulation for torsion dystonia in children.

作者信息

Alterman Ron L, Tagliati Michele

机构信息

Department of Neurosurgery, Mount Sinai Medical Center, One Gustave L. Levy Place, P.O. Box 1136, New York, NY 10029, USA.

出版信息

Childs Nerv Syst. 2007 Sep;23(9):1033-40. doi: 10.1007/s00381-007-0382-x. Epub 2007 Jun 6.

Abstract

INTRODUCTION

Deep brain stimulation (DBS) at the internal globus pallidus (GPi) is an effective treatment for some patients with medically refractory torsion dystonia. In this article, we review the results of pallidal DBS surgery in children with dystonia. Details of the DBS procedure and programming of the DBS devices are discussed.

DISCUSSION

Pallidal DBS is most effective in patients with primary generalized dystonia. Children and adolescents possessing the DYT1 gene mutation may respond best of all. The presence of static dystonic postures and/or fixed orthopedic contractures may limit the functional response to DBS and may require additional surgery.

CONCLUSION

As a group, patients with secondary dystonias respond less well to DBS than patients with primary dystonia. However, patients with dystonia secondary to anoxic brain injury who have grossly intact basal ganglia anatomy may represent a subpopulation for whom pallidal DBS is a viable option.

摘要

引言

内侧苍白球(GPi)深部脑刺激(DBS)是治疗某些药物难治性扭转性肌张力障碍患者的有效方法。在本文中,我们回顾了苍白球DBS手术治疗儿童肌张力障碍的结果。讨论了DBS手术过程及DBS设备的程控细节。

讨论

苍白球DBS对原发性全身性肌张力障碍患者最为有效。携带DYT1基因突变的儿童和青少年可能反应最佳。静态肌张力障碍姿势和/或固定的骨科挛缩的存在可能会限制对DBS的功能反应,可能需要额外的手术。

结论

作为一个群体,继发性肌张力障碍患者对DBS的反应不如原发性肌张力障碍患者。然而,基底节解剖结构大体完整的缺氧性脑损伤继发肌张力障碍患者可能是苍白球DBS可行的亚群体。

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