Absence seizures in lesion-related epilepsy

IF 1.2 Q4 CLINICAL NEUROLOGY Acta Epileptologica Pub Date : 2023-09-13 DOI:10.1186/s42494-023-00133-4
Xiaoqin Sun, Miao Wang, Zeng He, Lihong Liu, Xianjun Shi, Chunqing Zhang, Ning An, Meihua Yang, Zhifeng Wu, Ruodan Wang, Li Wang, Zhongke Wang, Hui Yang, Xiaolin Yang, Shiyong Liu
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Abstract

Abstract Background In the new International League Against Epilepsy (ILAE) classification of seizure types, generalized seizures such as absence seizures (ASs) may originate from a focal point and rapidly spread to the bilaterally distributed brain network. Increasing evidence from animal and clinical studies has indicated that focal changes may occur prior to ASs; however, the relationship of ASs with epileptogenic lesions remains unclear. Methods We retrospectively collected and analyzed the clinical, imaging, and electrophysiological data of 16 patients who had ASs and structural lesions with seizure-free outcomes after lesion resection. Results In semiology analysis, nine patients displayed focal onset; only two patients showed simple ASs, and seizure types other than ASs were observed in the remaining patients. On ictal electroencephalography (EEG), four patients showed bilateral synchronous symmetric 3 Hz generalized spike-wave discharges (GSWDs), and the remaining patients showed bilateral 1.5–2.5 Hz GSWDs. Moreover, most patients (13/16, 81.3%) exhibited focal features in addition to ASs, while interictal EEG was the same in 12 patients. Furthermore, on stereoelectroencephalogram (SEEG), 2/5 patients showed focal discharges before bilateral burst GSWDs. Additionally, all patients had structural lesions on imaging. In four typical AS patients, the lesions were located in deep brain regions. Notably, in 9 patients (9/16, 56%), the lesions were located in the posterior cortex. All patients underwent lesion resection and had seizure-free outcomes during follow-up, and intelligence quotient (IQ) also improved by 10.71 ± 3.90 one year after surgery. Conclusions Patients with lesion-related epilepsy may present with ASs that have a focal onset and are associated with good surgical outcomes.
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病变相关性癫痫的失神发作
背景:在新的国际抗癫痫联盟(ILAE)癫痫类型分类中,全面性癫痫发作(如失神发作(ASs))可能起源于一个焦点并迅速扩散到双侧分布的大脑网络。来自动物和临床研究的越来越多的证据表明,病灶改变可能发生在as之前;然而,as与癫痫性病变的关系尚不清楚。方法回顾性收集并分析16例as合并结构性病变患者的临床、影像学和电生理资料,病变切除后无癫痫发作。结果符号学分析中,9例患者表现为局灶性发病;仅有2例患者表现为单纯性急性发作,其余患者均出现非急性发作类型。4例患者脑电图显示双侧同步对称3hz广义尖峰波放电,其余患者为双侧1.5 ~ 2.5 Hz GSWDs。此外,大多数患者(13/16,81.3%)除as外还表现局灶性特征,其中12例患者间期EEG相同。此外,在立体脑电图(SEEG)上,2/5的患者在双侧爆发性GSWDs之前表现出局灶性放电。此外,所有患者在影像学上均有结构性病变。在4例典型AS患者中,病变位于脑深部。值得注意的是,9例(9/16,56%)患者的病变位于后皮层。所有患者均行病变切除,随访期间无癫痫发作,术后1年智商(IQ)提高10.71±3.90。结论病变相关性癫痫患者可能出现局灶性发作的急性脑梗死,并伴有良好的手术效果。
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来源期刊
Acta Epileptologica
Acta Epileptologica Medicine-Neurology (clinical)
CiteScore
2.00
自引率
0.00%
发文量
38
审稿时长
20 weeks
期刊最新文献
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