Involuntary movement is an uncommon manifestation of moyamoya disease. We describe a 12-year-old boy who suffered from involuntary movement after the first surgery but it improved dramatically after the second surgery...Involuntary movement is an uncommon manifestation of moyamoya disease. We describe a 12-year-old boy who suffered from involuntary movement after the first surgery but it improved dramatically after the second surgery. Initially, the patient underwent an encephalo-duro-arterio-myosynangiosis on the right side and encephalo-duro-periostealsynangiosis on the bifrontal side, which ameliorated his motor weakness in his left upper extremity. However, involuntary movement appeared in his right upper extremity. Secondly, the patient underwent encephalo-duro-arterio-myo-periostealsynangiosis on the left side. Thereafter, the patient’s involuntary movement completely resolved. The involuntary movement might occur due to the unequal distribution of the blood flow in the basal ganglia.展开更多
Focal dystonia in young aged patients is considered to be the uncommon clinical presentation, unless a secondary cause is to be considered. Infarcts of the corpus callosum are rare and have not been well documented pr...Focal dystonia in young aged patients is considered to be the uncommon clinical presentation, unless a secondary cause is to be considered. Infarcts of the corpus callosum are rare and have not been well documented previously. As for a variety of signs and symptoms due to corpus callosum lesion, focal dystonia can be easily overlooked. The case is approved by ethical committee and explained to the patient with patient approval.展开更多
氟哌噻吨美利曲辛导致的迟发性运动障碍(tardive dyskinesia,TD)少见文献报告。本文报告1例高龄女性混合性焦虑抑郁障碍患者,服用氟哌噻吨美利曲辛1年后,出现不自主口-舌-颊动作,异常不自主运动量表(abnormal involuntary movement scal...氟哌噻吨美利曲辛导致的迟发性运动障碍(tardive dyskinesia,TD)少见文献报告。本文报告1例高龄女性混合性焦虑抑郁障碍患者,服用氟哌噻吨美利曲辛1年后,出现不自主口-舌-颊动作,异常不自主运动量表(abnormal involuntary movement scale,AIMS)评分为12分,诊断为TD,停用氟哌噻吨美利曲辛,未作其它处理。停药后TD症状在短暂加重后逐渐减轻,1年后完全消除,再评AIMS为0分。其转归较为特殊,有别于以往关于TD“不可逆”的普遍认识,值得同行关注和讨论。展开更多
文摘Involuntary movement is an uncommon manifestation of moyamoya disease. We describe a 12-year-old boy who suffered from involuntary movement after the first surgery but it improved dramatically after the second surgery. Initially, the patient underwent an encephalo-duro-arterio-myosynangiosis on the right side and encephalo-duro-periostealsynangiosis on the bifrontal side, which ameliorated his motor weakness in his left upper extremity. However, involuntary movement appeared in his right upper extremity. Secondly, the patient underwent encephalo-duro-arterio-myo-periostealsynangiosis on the left side. Thereafter, the patient’s involuntary movement completely resolved. The involuntary movement might occur due to the unequal distribution of the blood flow in the basal ganglia.
文摘Focal dystonia in young aged patients is considered to be the uncommon clinical presentation, unless a secondary cause is to be considered. Infarcts of the corpus callosum are rare and have not been well documented previously. As for a variety of signs and symptoms due to corpus callosum lesion, focal dystonia can be easily overlooked. The case is approved by ethical committee and explained to the patient with patient approval.
文摘氟哌噻吨美利曲辛导致的迟发性运动障碍(tardive dyskinesia,TD)少见文献报告。本文报告1例高龄女性混合性焦虑抑郁障碍患者,服用氟哌噻吨美利曲辛1年后,出现不自主口-舌-颊动作,异常不自主运动量表(abnormal involuntary movement scale,AIMS)评分为12分,诊断为TD,停用氟哌噻吨美利曲辛,未作其它处理。停药后TD症状在短暂加重后逐渐减轻,1年后完全消除,再评AIMS为0分。其转归较为特殊,有别于以往关于TD“不可逆”的普遍认识,值得同行关注和讨论。
