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[岛叶癫痫。第1部分:症状学]

[Insular lobe epilepsy. Part 1: semiology].

作者信息

Hagiwara Koichi

机构信息

Epilepsy and Sleep Center, Fukuoka Sanno Hospital.

出版信息

Rinsho Shinkeigaku. 2024 Aug 27;64(8):527-539. doi: 10.5692/clinicalneurol.cn-001930-1. Epub 2024 Jul 27.

Abstract

The insula is often referred to as "the fifth lobe" of the brain, and its accessibility used to be very limited due to the deep location under the opercula as well as the sylvian vasculature. It was not until the availability of modern stereo-electroencephalography (SEEG) technique that the intracranial electrodes could be safely and chronically implanted within the insula, thereby enabling anatomo-electro-clinical correlations in seizures of this deep origin. Since the first report of SEEG-recorded insular seizures in late 1990s, the knowledge of insular lobe epilepsy (ILE) has rapidly expanded. Being on the frontline for the diagnosis and management of epilepsy, neurologists should have a precise understanding of ILE to differentiate it from epilepsies of other lobes or non-epileptic conditions. Owing to the multimodal nature and rich anatomo-functional connections of the insula, ILE has a wide range of clinical presentations. The following symptoms should heighten the suspicion of ILE: somatosensory symptoms involving a large/bilateral cutaneous territory or taking on thermal/painful character, and cervico-laryngeal discomfort. The latter ranges from slight dyspnea to a strong sensation of strangulation (laryngeal constriction). Other symptoms include epigastric discomfort/nausea, hypersalivation, auditory, vestibular, gustatory, and aphasic symptoms. However, most of these insulo-opercular symptoms can easily be masked by those of extra-insular seizure propagation. Indeed, sleep-related hyperkinetic (hypermotor) epilepsy (SHE) is a common clinical presentation of ILE, which shows predominant hyperkinetic and/or tonic-dystonic features that are often indistinguishable from those of fronto-mesial seizures. Subtle objective signs, such as constrictive throat noise (i.e., laryngeal constriction) or aversive behavior (e.g., facial grimacing suggesting pain), are often the sole clue in diagnosing insular SHE. Insular-origin seizures should also be considered in temporal-like seizures without frank anatomo-electro-clinical correlations. All in all, ILE is not the epilepsy of an isolated island but rather of a crucial hub involved in the multifaceted roles of the brain.

摘要

脑岛常被称为大脑的“第五叶”,由于其位于脑盖下方深处以及大脑外侧裂血管系统,过去很难对其进行研究。直到现代立体定向脑电图(SEEG)技术出现,才能够将颅内电极安全、长期地植入脑岛,从而实现对这种深部起源癫痫发作的解剖-电-临床关联研究。自20世纪90年代末首次报道SEEG记录的脑岛癫痫发作以来,岛叶癫痫(ILE)的相关知识迅速扩展。作为癫痫诊断和治疗的一线人员,神经科医生应准确了解ILE,以便将其与其他脑叶癫痫或非癫痫性疾病区分开来。由于脑岛具有多模态性质和丰富的解剖-功能连接,ILE有广泛的临床表现。以下症状应引起对ILE的怀疑:涉及大面积/双侧皮肤区域或具有热/疼痛特征的躯体感觉症状,以及颈-喉不适。后者范围从轻微呼吸困难到强烈的窒息感(喉部收缩)。其他症状包括上腹部不适/恶心、流涎过多、听觉、前庭、味觉和失语症状。然而,大多数这些脑岛-脑盖症状很容易被岛外癫痫传播的症状所掩盖。事实上,睡眠相关运动过多性(多动性)癫痫(SHE)是ILE的常见临床表现,其主要表现为多动性和/或强直性-肌张力障碍性特征,通常与额内侧癫痫发作难以区分。细微的客观体征,如收缩性喉音(即喉部收缩)或厌恶行为(例如,面部 grimacing 提示疼痛),往往是诊断脑岛SHE的唯一线索。在没有明确解剖-电-临床关联的类似颞叶癫痫发作中,也应考虑脑岛起源的癫痫发作。总之,ILE不是一个孤立的癫痫岛,而是一个参与大脑多方面功能的关键枢纽。

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