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儿童非典型良性部分性癫痫病例中的癫痫性负性肌阵挛:一项详细的视频多导记录研究

Epileptic negative myoclonus in a case of atypical benign partial epilepsy of childhood: a detailed video-polygraphic study.

作者信息

Fernández-Torre José L, Otero Benito

机构信息

Department of Clinical Neurophysiology, Hospital Universitario Marqués de Valdecilla, Santander, Spain.

出版信息

Seizure. 2004 Jun;13(4):226-34. doi: 10.1016/S1059-1311(03)00151-1.

Abstract

PURPOSE

To describe the clinical and electroencephalographic features of a child diagnosed as having atypical benign partial epilepsy (ABPE) who suffered from frequent lapses of postural tone in the right lower limb that were considered to represent a focal epileptic negative myoclonus (ENM).

MATERIAL AND METHODS

Electrophysiological evaluation included four serial waking and two sleep EEGs. Moreover, the investigation included a polygraphic recording with simultaneous video-EEG monitoring performed in rest, during hyperventilation, and while standing up with the aim of capturing patient's typical seizures.

RESULTS

During awake the EEG showed frequent bilateral centrotemporal discharges maximal over the left central area. Moreover, we recorded short generalised paroxysms of spike-and-wave discharges accompanied by a clear transient cognitive impairment that were in keeping with absences. We also captured several episodes of sudden and unexpected loss of postural tone in the right lower limb. These focal inhibitory seizures were associated with brief diffuse but asymmetrical paroxysms of irregular spike-and-wave discharges maximal over the left side. EMG flattening of the right quadriceps muscle was time-locked to the midline of the slow-wave component of the diffuse spike-and-wave discharges.

CONCLUSIONS

ENM leading to focal lapses of postural tone in lower extremities may be a predominant type of seizures in ABPE. A polygraphic recording with video-EEG monitoring is essential to confirm the diagnosis, and to detect other concomitant seizures, such as atypical absences. In our case, ENM could be more likely due to a transient disruption of cortical function.

摘要

目的

描述一名被诊断为非典型良性部分性癫痫(ABPE)的儿童的临床和脑电图特征,该患儿右下肢频繁出现姿势性肌张力丧失,被认为是局灶性癫痫性负性肌阵挛(ENM)。

材料与方法

电生理评估包括4次连续清醒脑电图和2次睡眠脑电图。此外,检查还包括在静息、过度换气和站立时进行同步视频脑电图监测的多导记录,目的是捕捉患者的典型发作。

结果

清醒时脑电图显示左侧中央区出现频繁的双侧中央颞区放电,且放电最强。此外,我们记录到伴有明显短暂认知障碍的短阵全身性棘慢波放电发作,符合失神发作。我们还捕捉到右下肢几次突然且意外的姿势性肌张力丧失发作。这些局灶性抑制性发作与左侧最强的短暂弥漫性但不对称的不规则棘慢波放电阵发有关。右侧股四头肌肌电图波幅降低与弥漫性棘慢波放电慢波成分的中线时间锁定。

结论

导致下肢局灶性姿势性肌张力丧失的ENM可能是ABPE中主要的发作类型。视频脑电图监测的多导记录对于确诊以及检测其他伴随发作(如非典型失神发作)至关重要。在我们的病例中,ENM更可能是由于皮质功能的短暂破坏所致。

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