Department of Neurology, Lahey Clinic, Burlington, Massachusetts 01805, USA.
J Neurosurg. 2010 Sep;113(3):634-8. doi: 10.3171/2010.1.JNS091127.
The authors report the cases of 2 young male patients (aged 16 and 26 years) with dystonic cerebral palsy of unknown origin, who developed status dystonicus, an acute and persistent combination of generalized dystonia and chorea. Both patients developed status dystonicus after undergoing general anesthesia, and in 1 case, after administration of metoclopramide. In attempting to control this acute hyperkinetic movement disorder, multiple medication trials failed in both cases and patients required prolonged intubation and sedation with propofol. Bilateral deep brain stimulation of the globus pallidus internus (4 and 2 months after the onset of symptoms in the first and second case, respectively) produced immediate resolution of the hyperkinetic movement disorder in each case. Deep brain stimulation provided persistent suppression of the dystonic movement potential after a follow-up of 30 and 34 months, respectively, as demonstrated by the reemergence of severe dystonia during the end of battery life of the implantable pulse generators that was readily controlled by exchange of the generators in each case.
作者报告了 2 例年轻男性患者(年龄分别为 16 岁和 26 岁),均患有不明原因的痉挛性脑瘫,出现张力障碍状态,即全身性肌张力障碍和舞蹈症的急性持续组合。这 2 例患者均在全身麻醉后发生张力障碍状态,1 例在使用甲氧氯普胺后发生。在试图控制这种急性运动障碍时,2 例患者均尝试了多种药物治疗,但均失败,需要长时间使用异丙酚进行插管和镇静。双侧苍白球 internus 深部脑刺激(第 1 例和第 2 例分别在症状出现后 4 个月和 2 个月)使每个病例的运动障碍均立即得到缓解。深部脑刺激分别在 30 个月和 34 个月的随访中持续抑制张力障碍运动电位,在每个病例中,当可植入脉冲发生器的电池寿命接近尾声时,严重的张力障碍再次出现,通过更换发生器可轻易控制。