A generalized seizure type: Myoclonic-to-tonic seizure

IF 3.7 3区 医学 Q1 CLINICAL NEUROLOGY Clinical Neurophysiology Pub Date : 2024-04-23 DOI:10.1016/j.clinph.2024.04.011
Zongpu Zhou , Pan Gong , Xianru Jiao , Yue Niu , Zhao Xu , Jiong Qin , Zhixian Yang
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Abstract

Background and purpose

To test the hypothesis that myoclonic seizures can evolve to tonic seizures, we documented the electroclinical features of this under-recognized seizure type.

Methods

We observed a distinct seizure pattern starting with myoclonus without returning to an interictal state, which subsequently evolved into generalized tonic seizures. The detailed symptomatic and electroencephalographic characteristics of this seizure were extracted, and the clinical manifestations, drug curative responses in patients with this seizure were reviewed and analyzed.

Results

The onset of all seizures was characterized by a preceding period of myoclonus and bursts of generalized spike or poly-spike slow wave discharges with high amplitude. This was closely followed by the occurrence of tonic seizures, which were distinguished by bursts of generalized fast activity at 10 Hz or higher frequency. This under-recognized seizure type has been designated as myoclonic-to-tonic (MT) seizure. The number of patients identified with MT seizures in this study was 34. The prevalence rate of MT seizures was found to be higher in males. While MT seizures typically included a tonic component, it should be noted that some patients experiencing this seizure type never presented with isolated tonic seizures. Generalized Epilepsy not further defined (GE) accounted for approximately one-third of the diagnosed cases, followed by Lennox-Gastaut syndrome and Epilepsy with Myoclonic-Atonic seizures. In comparison to other types of epilepsy, GE with MT seizures demonstrated a more favorable prognosis.

Conclusions

The classification of myoclonic-to-tonic seizure represents a novel approach in comprehending the ictogenesis of generalized seizures and can provide valuable assistance to clinicians in epilepsy diagnosis.

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一种全身性发作类型:肌阵挛转强直性发作
背景和目的为了验证肌阵挛发作可演变为强直性发作的假设,我们记录了这一未被充分认识的发作类型的电临床特征。方法我们观察到一种独特的发作模式,从肌阵挛开始,不返回发作间期状态,随后演变为全身强直性发作。结果所有癫痫发作的起始阶段都有一段肌阵挛和一阵阵高振幅的全身性棘波或多棘慢波放电。紧随其后的是强直性发作,其特征是频率为 10 赫兹或更高的阵发性全身快速活动。这种未被充分认识的发作类型被称为肌阵挛强直(MT)发作。在这项研究中,被确认为 MT 发作的患者人数为 34 人。研究发现,男性的MT发作患病率较高。虽然 MT 癫痫发作通常包括强直性成分,但应该注意的是,一些经历过这种发作类型的患者从未出现过孤立的强直性发作。未进一步界定的全身性癫痫(GE)约占确诊病例的三分之一,其次是伦诺克斯-加斯豪特综合征(Lennox-Gastaut syndrome)和肌阵挛-强直性癫痫。与其他类型的癫痫相比,伴有MT发作的全身性癫痫的预后较好。结论肌阵挛-强直发作的分类是理解全身性癫痫发作机制的一种新方法,可为临床医生的癫痫诊断提供有价值的帮助。
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来源期刊
Clinical Neurophysiology
Clinical Neurophysiology 医学-临床神经学
CiteScore
8.70
自引率
6.40%
发文量
932
审稿时长
59 days
期刊介绍: As of January 1999, The journal Electroencephalography and Clinical Neurophysiology, and its two sections Electromyography and Motor Control and Evoked Potentials have amalgamated to become this journal - Clinical Neurophysiology. Clinical Neurophysiology is the official journal of the International Federation of Clinical Neurophysiology, the Brazilian Society of Clinical Neurophysiology, the Czech Society of Clinical Neurophysiology, the Italian Clinical Neurophysiology Society and the International Society of Intraoperative Neurophysiology.The journal is dedicated to fostering research and disseminating information on all aspects of both normal and abnormal functioning of the nervous system. The key aim of the publication is to disseminate scholarly reports on the pathophysiology underlying diseases of the central and peripheral nervous system of human patients. Clinical trials that use neurophysiological measures to document change are encouraged, as are manuscripts reporting data on integrated neuroimaging of central nervous function including, but not limited to, functional MRI, MEG, EEG, PET and other neuroimaging modalities.
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