Neth Bryan J, Mustafa Rafid
Department of Neurology, Mayo Clinic, Rochester, MN, USA.
Neurohospitalist. 2024 Apr;14(2):220-221. doi: 10.1177/19418744231210038. Epub 2023 Nov 5.
A 70-year-old male without prior psychiatric history presented with recurrent episodes (<60 seconds each, every 5-10 minutes) of left hemibody and right lower extremity jerking movements concerning for seizure with preserved awareness (Video). Examination showed left hemiparesis (leg > arm) in addition to right lower extremity weakness. Computed tomography showed a right parafalcine acute subdural hematoma (SDH). Clinical events did not recur after intravenous lorazepam (4 mg) and levetiracetam load (3500 mg), and his weakness improved. He was continued on levetiracetam and has since remained seizure free for 16 months. A 60-minute awake/sleep electroencephalogram (EEG) obtained 12 hours after administration of antiseizure medications showed low amplitude theta slowing (posterior predominant) in the range of 5-7 Hz. There was no apparent epileptiform activity or other abnormalities during the awake and sleep recording or photic stimulation. Focal seizures originate from pathologic disruption of neuronal activity within an isolated brain region, almost exclusively from a single hemisphere. Focal seizures may generalize bilaterally with associated impaired awareness. This is the first visual report demonstrating focal, bihemispheric clinical seizures, without generalization or impaired awareness. Rarely patients with generalized motor involvement from seizures have had retained consciousness and memory. The parafalcine SDH likely promoted epileptogenicity of the bilateral hemispheres. Acute and chronic SDH commonly present with seizures. Although there were no supportive electrographic findings, parasagittal epileptogenic lesions may be difficult for both clinical and electrographic localization. Post-event paresis with clinical improvement in the hours after event cessation supports clinical seizure.
一名70岁男性,既往无精神病史,出现反复发作(每次<60秒,每5 - 10分钟发作一次)的左半侧身体和右下肢抽搐运动,考虑为发作时意识保留的癫痫(视频)。检查发现除右下肢无力外,还有左侧偏瘫(腿部>手臂)。计算机断层扫描显示右侧大脑镰旁急性硬膜下血肿(SDH)。静脉注射劳拉西泮(4毫克)和负荷剂量左乙拉西坦(3500毫克)后临床事件未再复发,且他的无力症状有所改善。此后继续使用左乙拉西坦,自那以后16个月未再发作。在服用抗癫痫药物12小时后进行的一次60分钟清醒/睡眠脑电图(EEG)检查显示,在5 - 7赫兹范围内有低幅θ波减慢(以枕部为主)。在清醒和睡眠记录以及闪光刺激期间,没有明显的癫痫样活动或其他异常。局灶性癫痫发作源于孤立脑区内神经元活动的病理性破坏,几乎完全来自单个半球。局灶性癫痫发作可能双侧泛化并伴有意识障碍。这是第一份视觉报告,展示了局灶性、双侧半球临床癫痫发作,无泛化或意识障碍。极少有癫痫发作导致全身运动受累的患者能保持意识和记忆。大脑镰旁SDH可能促进了双侧半球的致痫性。急性和慢性SDH通常伴有癫痫发作。尽管没有支持性的脑电图结果,但矢状窦旁致痫性病变在临床和脑电图定位上可能都很困难。事件发生后出现的肢体无力在事件停止后的数小时内临床症状改善,支持临床癫痫发作的诊断。