Fuller Jonathan, Prescott Ian A, Moro Elena, Toda Hiroki, Lozano Andres, Hutchison William D
Faculty of Medicine, University of Toronto, Toronto, Ont., Canada.
Stereotact Funct Neurosurg. 2013;91(3):190-7. doi: 10.1159/000345113. Epub 2013 Feb 27.
The efficacy of bilateral globus pallidus internus (GPi) deep brain stimulation (DBS) for medically refractory idiopathic generalized dystonia has been demonstrated repeatedly. More variable outcomes have been reported in the treatment of secondary dystonia with GPi DBS.
The present study seeks to examine the pallidal physiology and clinical outcome of GPi DBS in a case of secondary dystonia.
We report on a 43-year-old man who at the age of 9 suffered a left basal ganglia stroke and at the age of 21 developed severe disabling hemidystonia. Following unsuccessful medical management for many years and an axial involvement of the dystonia, he underwent bilateral GPi DBS with dual microelectrode mapping of cell firing and evoked field potentials (fEP).
On the intact side we found regular firing of pallidal neurons and normal fEP indicative of functioning striatopallidal pathways. The affected side was found to include a higher frequency of bursting pallidal neurons. fEP could not be evoked on the affected side, suggesting their origin to be striatal GABAergic afferents.
The patient had marked benefit from bilateral GPi DBS, which suggests that the therapeutic effects of DBS were mediated by the intact pathways in this case of hemidystonia.
双侧苍白球内侧部(GPi)深部脑刺激(DBS)治疗药物难治性特发性全身性肌张力障碍的疗效已得到反复证实。关于GPi DBS治疗继发性肌张力障碍的结果报道则更具变异性。
本研究旨在探讨1例继发性肌张力障碍患者接受GPi DBS治疗时的苍白球生理学及临床疗效。
我们报告1例43岁男性,其9岁时发生左侧基底节卒中,21岁时出现严重致残性偏侧肌张力障碍。在多年药物治疗失败且肌张力障碍累及轴性肌肉后,他接受了双侧GPi DBS治疗,并采用双微电极记录细胞放电及诱发场电位(fEP)。
在未受累侧,我们发现苍白球神经元放电规律,fEP正常,提示纹状体 - 苍白球通路功能正常。在受累侧,发现爆发性放电的苍白球神经元频率更高。在受累侧无法诱发出fEP,提示其起源于纹状体GABA能传入纤维。
该患者从双侧GPi DBS治疗中获益显著,这表明在该例偏侧肌张力障碍中,DBS的治疗效果是由完整的通路介导的。