Casaubon Leanne, Pohlmann-Eden Bernd, Khosravani Houman, Carlen Peter L, Wennberg Richard
Krembil Neuroscience Centre, Toronto Western Hospital, University of Toronto, Toronto, ON, Canada.
Epileptic Disord. 2003 Sep;5(3):149-56.
Whether cortical or subcortical structures, specifically the thalamus, play the dominant role in generating primary generalized seizures has been the subject of long debate. Most experimental data implicate a hyperexcitable cortical generator of spike-and-wave activity, with the thalamus quickly recruited to sustain the generalized oscillations through a reverberating thalamocortical network. However, there is little clinical evidence to support the cortical generator hypothesis. We present video-EEG recordings of generalized tonic-clonic seizures in three patients with proven primary generalized epilepsy (PGE), all of whom showed a consistent pattern of lateralized seizure onset compatible with a focal frontal lobe generator.
Among 300 patients referred for video-EEG monitoring for intractable epilepsy, three were found to have PGE with tonic-clonic convulsions. All had a positive family history for epilepsy and no other epilepsy risk factors. Epilepsy onset was during adolescence (2/3) or childhood (1/3). Patients were taking 1-4 antiepileptic drugs (AEDs) at admission, none of which was valproic acid.
Interictal EEG showed very active, bilaterally synchronous generalized spike-and-wave or polyspike-and-wave discharges between 2.5-4.5 Hz, maximal over the midfrontal structures symmetrically in all patients. Ictal EEG showed generalized rhythmic activity without lateralization at seizure onset. Surprisingly, in all 6 recorded tonic-clonic seizures there was a sustained (10-15 seconds), stereotyped, clinical lateralization at onset, which took the form of a tonic "fencing posture" in one patient (two seizures) and forced head/eye/torso version in two patients (four seizures). Two patients became seizure-free shortly after switching to valproate monotherapy. One patient refused valproate but has improved more than 90% with a change in AEDs to lamotrigine and phenobarbital (follow-up in all patients>18 months).
Tonic-clonic seizures are presumed to be generalized from onset in patients with PGE. However, video-EEG monitoring in these patients is rarely performed and the actual clinical features of the seizures maybe underappreciated. The demonstration of sustained lateralization at onset in our patients, with features clinically indistinguishable from focal onset frontal lobe seizures, is compatible with the hypothesis of a focal region of cortical hyperexcitability situated in the frontal lobes of some patients with PGE. Whether this cortical generator is autonomous or "triggered" by ascending, possibly normal, thalamocortical volleys is unresolved.
无论是皮质结构还是皮质下结构,特别是丘脑,在原发性全面性癫痫发作的产生中是否起主导作用一直是长期争论的话题。大多数实验数据表明,棘波和慢波活动的皮质过度兴奋发生器是存在的,丘脑通过丘脑皮质回响网络迅速被募集以维持全面性振荡。然而,几乎没有临床证据支持皮质发生器假说。我们展示了3例确诊为原发性全面性癫痫(PGE)患者的全身强直阵挛性发作的视频脑电图记录,所有患者均表现出与局灶性额叶发生器相符的一致的发作起始侧化模式。
在300例因难治性癫痫接受视频脑电图监测的患者中,发现3例患有PGE并伴有强直阵挛性惊厥。所有患者均有癫痫家族史,无其他癫痫危险因素。癫痫发作始于青春期(2/3)或儿童期(1/3)。患者入院时服用1 - 4种抗癫痫药物(AEDs),均非丙戊酸。
发作间期脑电图显示,所有患者双侧同步的2.5 - 4.5Hz棘波和慢波或多棘波和慢波放电非常活跃,在额中结构处最为明显且对称。发作期脑电图显示发作起始时无侧化的全面性节律性活动。令人惊讶的是,在所有记录的6次强直阵挛性发作中,发作起始时均有持续(10 - 15秒)、刻板的临床侧化,其中1例患者(2次发作)表现为强直“击剑姿势”,2例患者(4次发作)表现为强迫性头/眼/躯干转向。2例患者在改用丙戊酸单药治疗后不久癫痫发作停止。1例患者拒绝使用丙戊酸,但改用拉莫三嗪和苯巴比妥后病情改善超过90%(所有患者随访>18个月)。
PGE患者的强直阵挛性发作通常被认为从发作开始就是全面性的。然而,这些患者很少进行视频脑电图监测,癫痫发作的实际临床特征可能未得到充分认识。我们的患者发作起始时出现持续侧化,其特征在临床上与局灶性发作的额叶癫痫难以区分,这与部分PGE患者额叶皮质存在过度兴奋局灶区域的假说相符。这种皮质发生器是自主的还是由上升的、可能正常的丘脑皮质冲动“触发”的,目前尚无定论。