Zidverc-Trajković Jasna, Jovanović Dejana R, Marjanović Ivan, Radojičić Aleksandra, Beslać-Bumbaširević Ljiljana
Institute of Neurology, School of Medicine, Clinical Centre of Serbia, Belgrade, Serbia.
Neurologist. 2011 Jul;17(4):205-7. doi: 10.1097/NRL.0b013e31821a25c4.
Hemiballism (HB) is a relatively rare hyperkinetic disorder commonly caused by an acute stroke. Such patients usually receive symptomatic therapy with limited effect. We report the case of an acute stroke patient with HB who was successfully treated with intravenous recombinant tissue plasminogen activator (rtPA).
A 67-year-old man with a history of hypertension and ischemic coronary heart disease presented in the emergency room 85 minutes after sudden onset of involuntary coarse flinging movements of the left arm and leg. Neurological investigation revealed oromandibular dyskinesia; left blepharospasm; dyskinetic movements of the head and neck; dysarthria; and forceful, jerky, irregular, flinging, large-amplitude involuntary movements involving his left arm and left leg. Initial brain computed tomography showed only mild confluent periventricular hypodensities in the vicinity of the frontal horns. The calculated National Institutes of Health Stroke Scale score was 1, for dysarthria. The sudden onset of HB, however, suggested an acute stroke and we decided to treat the patient with intravenous rtPA. Thrombolytic therapy with rtPA began 200 minutes after symptom onset, and after the patient's increased arterial blood pressure was resolved. Follow-up examination performed 12 hours after therapy revealed only mild dysarthria; mild ataxia of the left arm, and ataxic gait. Delayed brain computed tomography did not indicate recent ischemia, although a fluid attenuated inversion recovery magnetic resonance imaging sequence revealed high signal intensity lesions in the vicinity of the right putamen and left cerebellar hemisphere. After 1 month, a follow-up examination revealed only mild dysarthria and mild ataxia of the left arm.
Acute stroke patients with low National Institutes of Health Stroke Scale score, including patients with HB, should be considered as candidates for thrombolytic treatment.
偏身投掷症(HB)是一种相对罕见的运动亢进性疾病,通常由急性中风引起。此类患者通常接受对症治疗,但效果有限。我们报告一例急性中风合并偏身投掷症患者,经静脉注射重组组织型纤溶酶原激活剂(rtPA)成功治疗。
一名67岁男性,有高血压和缺血性冠心病病史,在左臂和左腿突然出现不自主粗大投掷运动85分钟后就诊于急诊室。神经系统检查发现口下颌运动障碍;左侧眼睑痉挛;头颈部运动障碍;构音障碍;以及涉及左臂和左腿的有力、急促、不规则、投掷样、大幅度不自主运动。初始脑部计算机断层扫描仅显示额角附近轻度融合性脑室周围低密度影。计算得出的美国国立卫生研究院卒中量表评分为1分,原因是构音障碍。然而,偏身投掷症的突然发作提示急性中风,我们决定对该患者进行静脉rtPA治疗。在症状发作200分钟后,且患者升高的动脉血压得到控制后,开始rtPA溶栓治疗。治疗后12小时进行的随访检查仅发现轻度构音障碍;左臂轻度共济失调,以及共济失调步态。延迟脑部计算机断层扫描未显示近期缺血,尽管液体衰减反转恢复磁共振成像序列显示右侧壳核和左侧小脑半球附近有高信号强度病变。1个月后,随访检查仅发现轻度构音障碍和左臂轻度共济失调。
美国国立卫生研究院卒中量表评分较低的急性中风患者,包括偏身投掷症患者,应被视为溶栓治疗的候选者。