Focal negative motor seizures: Multimodal evaluation.

IF 6.6 1区 医学 Q1 CLINICAL NEUROLOGY
Epilepsia Pub Date : 2024-11-22 DOI:10.1111/epi.18191
Roberta Di Giacomo, Rachele Colombo, Laura Canafoglia, Dunja Duran, Chiara Pastori, Andrea Stabile, Giulia Battaglia, Giuseppe Didato, Valeria Cuccarini, Francesco Deleo, Ambra Dominese, Marco de Curtis, Davide Rossi Sebastiano
{"title":"Focal negative motor seizures: Multimodal evaluation.","authors":"Roberta Di Giacomo, Rachele Colombo, Laura Canafoglia, Dunja Duran, Chiara Pastori, Andrea Stabile, Giulia Battaglia, Giuseppe Didato, Valeria Cuccarini, Francesco Deleo, Ambra Dominese, Marco de Curtis, Davide Rossi Sebastiano","doi":"10.1111/epi.18191","DOIUrl":null,"url":null,"abstract":"<p><p>This case report shows the importance of multimodal evaluation to formulate a proper diagnosis of negative motor seizures (NMSs). Only few reports in literature document NMSs with video-electroencephalographic (EEG) and electromyographic coregistration. A multimodal evaluation is crucial to exclude common mimics and propose correct therapy. We describe a case of a 62-year-old man with drug-resistant focal epilepsy and NMSs, evaluated with video-EEG recording with polygraphy, magnetoencephalography (MEG), and brain magnetic resonance imaging (MRI). Video-EEG monitoring showed 182 focal NMSs, with preserved awareness and comprehension. The patient reported complex paresthesia of the left hand followed by left facial grimace, left arm flaccid paralysis, and bradycardia. EEG showed ictal discharges in the right frontocentral region associated with sudden electromyographical silence in left limb muscles consistent with loss of tonic contraction from distal to proximal muscles of the arm. MEG localized the epileptic zone in the right opercular region, consistent with MRI evidence of type II cortical dysplasia in the right inferior frontal gyrus. Multimodal evaluation is essential to document the temporal relationship between ictal discharges, clinical onset of limb paresis, and electrophysiologic evidence of loss of tonic muscular contraction. It allows definition of the specific cortical area involved in NMSs, offering new insight into physiological brain functioning.</p>","PeriodicalId":11768,"journal":{"name":"Epilepsia","volume":" ","pages":""},"PeriodicalIF":6.6000,"publicationDate":"2024-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Epilepsia","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/epi.18191","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

This case report shows the importance of multimodal evaluation to formulate a proper diagnosis of negative motor seizures (NMSs). Only few reports in literature document NMSs with video-electroencephalographic (EEG) and electromyographic coregistration. A multimodal evaluation is crucial to exclude common mimics and propose correct therapy. We describe a case of a 62-year-old man with drug-resistant focal epilepsy and NMSs, evaluated with video-EEG recording with polygraphy, magnetoencephalography (MEG), and brain magnetic resonance imaging (MRI). Video-EEG monitoring showed 182 focal NMSs, with preserved awareness and comprehension. The patient reported complex paresthesia of the left hand followed by left facial grimace, left arm flaccid paralysis, and bradycardia. EEG showed ictal discharges in the right frontocentral region associated with sudden electromyographical silence in left limb muscles consistent with loss of tonic contraction from distal to proximal muscles of the arm. MEG localized the epileptic zone in the right opercular region, consistent with MRI evidence of type II cortical dysplasia in the right inferior frontal gyrus. Multimodal evaluation is essential to document the temporal relationship between ictal discharges, clinical onset of limb paresis, and electrophysiologic evidence of loss of tonic muscular contraction. It allows definition of the specific cortical area involved in NMSs, offering new insight into physiological brain functioning.

局灶性阴性运动性癫痫发作:多模式评估
本病例报告显示了多模态评估对于正确诊断阴性运动性癫痫发作(NMS)的重要性。文献中只有极少数报告记录了视频脑电图(EEG)和肌电图核心连接的 NMS。多模态评估对于排除常见的拟态并提出正确的治疗方案至关重要。我们描述了一例 62 岁男性患者的病例,他患有耐药性局灶性癫痫和 NMS,通过视频脑电图记录和多导图、脑磁图(MEG)和脑磁共振成像(MRI)对其进行了评估。视频脑电图监测显示,患者出现了 182 次局灶性 NMS,但意识和理解能力均得到了保留。患者称左手有复杂的麻痹感,随后出现左脸狰狞、左臂弛缓性麻痹和心动过缓。脑电图显示,右侧前中央区有发作性放电,左侧肢体肌肉突然出现肌电图沉默,与手臂远端到近端肌肉失去强直性收缩一致。脑电图将癫痫区定位在右侧厣区,与核磁共振成像显示的右侧额叶下回 II 型皮质发育不良相一致。多模态评估对于记录发作性放电、肢体瘫痪的临床发作和强直性肌肉收缩丧失的电生理学证据之间的时间关系至关重要。它可以确定NMSs所涉及的特定皮质区域,为了解大脑的生理功能提供新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Epilepsia
Epilepsia 医学-临床神经学
CiteScore
10.90
自引率
10.70%
发文量
319
审稿时长
2-4 weeks
期刊介绍: Epilepsia is the leading, authoritative source for innovative clinical and basic science research for all aspects of epilepsy and seizures. In addition, Epilepsia publishes critical reviews, opinion pieces, and guidelines that foster understanding and aim to improve the diagnosis and treatment of people with seizures and epilepsy.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信