Mayville C, Fakhoury T, Abou-Khalil B
Department of Neurology, Vanderbilt University, Nashville, Tennessee, USA.
Epilepsia. 2000 Apr;41(4):391-4. doi: 10.1111/j.1528-1157.2000.tb00178.x.
To report the clinical and electrographic features of absence seizures evolving into generalized tonic-clonic (GTC) activity in six patients with idiopathic generalized epilepsy.
All patients were referred for evaluation of refractory seizures and underwent video-EEG monitoring after discontinuation of their antiepileptic drugs (AEDs). We analyzed the video-EEG recordings for seizure semiology as well as ictal and interictal activity. We also reviewed the initial clinical data in all patients.
All patients were women, with a mean age of 27 years (range, 14-43 years). The mean age at seizure onset was 12 years (range, 5-15 years). Family history was positive for epilepsy in four patients. All patients had recorded seizures with an onset that was characteristic of generalized absence clinically and electrographically, with evolution into GTC activity. The EEG onset was with generalized 2.5-to 5-Hz spike-and-wave discharges, with evolution into faster rhythmic activity. Interictal EEG recordings showed generalized 2-to 5-Hz spike-and-wave discharges. All had normal background activity. All patients were treated with divalproex monotherapy. Five patients have been seizure free, and one had a single breakthrough GTC seizure during a follow-up period of 12-36 months.
GTC activity may evolve from typical absence seizures. This seizure type should be included in the International Classification of Seizures. Its recognition and distinction from complex partial seizures with secondary generalization are important for appropriate therapy.
报告6例特发性全身性癫痫患者失神发作演变为全身强直-阵挛(GTC)发作的临床和脑电图特征。
所有患者因难治性癫痫发作前来评估,在停用抗癫痫药物(AEDs)后接受视频脑电图监测。我们分析了视频脑电图记录的发作症状学以及发作期和发作间期的活动情况。我们还回顾了所有患者的初始临床资料。
所有患者均为女性,平均年龄27岁(范围14 - 43岁)。癫痫发作的平均起始年龄为12岁(范围5 - 15岁)。4例患者有癫痫家族史。所有患者记录到的发作在临床和脑电图上均具有全身性失神发作的特征,并演变为GTC发作。脑电图发作起始为全身性2.5至5赫兹棘慢波放电,随后演变为更快的节律性活动。发作间期脑电图记录显示全身性2至5赫兹棘慢波放电。所有患者背景活动均正常。所有患者均接受丙戊酸单药治疗。5例患者无癫痫发作,1例在12至36个月的随访期内有1次突破性GTC发作。
GTC发作可能由典型失神发作演变而来。这种发作类型应纳入国际癫痫发作分类中。对其进行识别并与继发全身性发作的复杂部分性发作相区分,对于恰当治疗很重要。