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颞叶极部病变患者的运动过多性癫痫发作。

Hypermotor seizures in patients with temporal pole lesions.

作者信息

Wang Lina, Mathews Gregory C, Whetsell William O, Abou-Khalil Bassel

机构信息

Department of Neurology, Vanderbilt University Medical Center, United States.

出版信息

Epilepsy Res. 2008 Nov;82(1):93-98. doi: 10.1016/j.eplepsyres.2008.07.005. Epub 2008 Aug 29.

Abstract

Hypermotor seizures are considered to be characteristic of frontal lobe epilepsy, with only rare occurrence in temporal lobe epilepsy. After noting hypermotor seizures in several patients with lesions involving the pole of the temporal lobe, we investigated whether temporal pole lesions were associated with hypermotor seizures. We systematically reviewed medical records, MRI images and pathological findings in consecutive patients who underwent epilepsy surgery over the preceding 10 years in our institution and identified eight patients with temporal pole lesions and intractable complex partial seizures. We analyzed all recorded seizures for semiology, classifying seizures as hypermotor or typical "psychomotor." Four patients exhibited hypermotor seizure semiology and four patients manifested typical psychomotor seizure characteristics. In patients with hypermotor seizures, scalp EEG tended to demonstrate lateral anterior temporal ictal onset, with lesser involvement of the sphenoidal electrode, while the patients with psychomotor seizures had initial inferomesial temporal rhythmic theta activity. Two patients with hypermotor seizures had implanted frontal and temporal subdural grids demonstrating orbitofrontal spread before hypermotor behavior. Patients underwent either anterior temporal lobectomy or lesionectomy. All improved considerably, with six patients seizure-free since surgery. We conclude that hypermotor seizures occur frequently in patients with temporal pole lesions. A search for temporal pole pathology is recommended for patients with hypermotor seizures and temporal epileptiform discharges. Modification of the surgical approach to include this region should be considered in patients who exhibit hypermotor seizures.

摘要

运动过多性癫痫发作被认为是额叶癫痫的特征,在颞叶癫痫中仅罕见发生。在注意到几名颞叶极部有病变的患者出现运动过多性癫痫发作后,我们研究了颞叶极部病变是否与运动过多性癫痫发作有关。我们系统回顾了本机构在过去10年接受癫痫手术的连续患者的病历、MRI图像和病理结果,确定了8例有颞叶极部病变和难治性复杂部分性癫痫发作的患者。我们分析了所有记录的癫痫发作的症状学,将癫痫发作分类为运动过多性或典型的“精神运动性”。4例患者表现出运动过多性癫痫发作症状学,4例患者表现出典型的精神运动性癫痫发作特征。在运动过多性癫痫发作的患者中,头皮脑电图倾向于显示颞叶前部外侧发作起始,蝶骨电极受累较少,而精神运动性癫痫发作的患者最初有颞叶内侧下部节律性θ活动。2例运动过多性癫痫发作的患者植入了额叶和颞叶硬膜下网格,显示在运动过多行为之前眶额部扩散。患者接受了前颞叶切除术或病灶切除术。所有患者均有显著改善,6例患者术后无癫痫发作。我们得出结论,运动过多性癫痫发作常见于有颞叶极部病变的患者。对于有运动过多性癫痫发作和颞叶癫痫样放电的患者,建议寻找颞叶极部病变。对于表现出运动过多性癫痫发作的患者,应考虑修改手术方法以包括该区域。

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