颅内电极埋藏在枕叶癫痫中的作用

目的探讨运用颅内电极埋藏进行视频脑电图监测在定位困难的枕叶癫痫中的作用。方法通过对9例枕叶癫痫但定侧定位困难的患者,向颅内可疑部位植入硬膜下条状电极,进行视频脑电图监测,记录发作间期及发作期脑电图变化,确定癫痫病灶起始区。通过手术切除致痫灶。结果本组9例埋藏时间为3～9d,平均5d,均记录到间歇期痫样放电及发作期脑电图情况。行枕叶局部皮层切除6例及枕叶切除3例。术后按照Engel评分,I级7例,II级2例。所有病例均未出现埋藏电极引起的并发症。结论在致痫灶定位困难的顽固性枕叶癫痫中,采用颅内电极埋藏进行脑电图监测,可以精确定位致痫灶,从而提高癫痫的治愈率。     

颅内电极监测对顽固性颞叶癫痫致痫灶的定位价值

目的:探讨发作期及发作间期颅内电极监测对癫痫灶的定位作用。方法:20例难治性颞叶癫痫,经临床、影像学及头皮脑电图不能确定致痫灶部位,应用立体定向技术,在患者双侧颞叶植入硬膜下条状电极,进行长时间视频脑电图监测,记录发作期和发作间期的脑电图变化,并与头皮脑电图、MRI进行比较,分析癫痫灶部位,进行手术治疗,术后跟踪随访,评估致痫灶定位的准确性。结果:20例癫痫病人颅内电极埋藏时间1～5天,每个患者至少监测到2次临床发作,每一病例均记录发作间期和发作期的异常放电活动。15例发作间期与发作期定侧一致,2例发作间期为双侧棘波病灶,3例发作间期定位与发作期不一致。按Engel术后效果分级:手术效果满意(癫痫发作消失)13例(65%),显著改善3例(15%),良好3例(15%),无效1例(5%)。所有病例均未出现因颅内电极埋藏而致的并发症。结论:对于致痫灶不能定位的难治性癫痫,应用颅内电极记录方法,尤其是发作期起始时脑电图变化,可以确定致痫灶位置,为癫痫手术治疗提供可靠的依据。     

颞叶癫痫的手术治疗(附34例分析)

目的　探讨颞叶癫痫的术前评估和术式选择策略。方法　对 34例颞叶癫痫患者应用无创和有创方法进行术前综合评估 ,采用扩大额颞问号式手术切口 ,经外侧裂入路、皮层脑电监测引导下实施手术。对术前评估方法、术中脑电监测的意义和手术方式选择进行了分析。结果　 2 1例患者根据长程蝶骨电极脑电图和MRI等无创检查定位了致痫灶 ,13例根据颅内埋置电极脑电图定位了致痫灶。术后随访 15 .6± 6 .0月。 2 9例 (85 .3% )癫痫发作消失 ,3例 (8.8% )发作减少 75 % ,2例 (5 .9% )发作减少 5 0 %以上。 8例曾出现短期并发症 ,无永久性并发症发生。手术 6个月后 ,患者的日常生活能力评分与手术前相比明显改善 (P <0 .0 5 )。结论　长程视频脑电图和MRI检查是颞叶癫痫致痫灶定位可靠的无创性检查方法 ;颅内埋置电极检查是术前准确定位致痫灶必要的手段。颅内电极脑电图监测对设计切除方式有重要参考价值 ;改良的手术切口和经外侧裂入路有利于安全有效的切除前颞叶或选择性切除颞叶内侧结构     

6例磁共振阴性额叶癫痫患者致痫灶定位研究

目的探讨硬膜下电极脑电图(ECo G)监测对磁共振阴性癫痫患者致痫灶的定位作用。方法对经临床、影像学和头皮EEG检查不能确定致痫灶部位的6例难治性额叶癫痫患者,植入硬膜下条状电极进行视频EEG监测,观察颅内电极发作期及发作间期EEG变化,结合头皮EEG、临床发作结果对癫痫灶进行综合定位;术后随访,评估致痫灶定位的准确性。结果 6例患者颅内电极埋藏时间为2~5 d,每例监测到2次临床发作并记录发作间期和发作期的异常放电活动。5例患者发作期颅内电极EEG均能准确定位,5例显示一侧局灶性放电起源,1例患者显示双侧放电起源。术后按Engel疗效分级:EngelⅠ级4例(57.1%),EngelⅡ级1例(14.3%),随访不满1年的按谭氏术后效果分级,达到了满意。结论颅内电极EEG监测可为癫痫手术治疗提供可靠的病灶定位依据。     

枕叶癫痫的术前定位

目的:通过回顾分析9例枕叶癫痫患者的临床资料,讨论枕叶癫痫的临床特征和致痫灶的术前定位。方法:应用临床发作症状评估、CT/MRI扫描、SPECT/PET检查、长程视频脑电图监测、颅内电极记录以及皮层脑电监测等方法综合定位枕叶癫痫患者的致痫灶。结果:视觉先兆及头或眼向一侧偏转是最常见的发作早期改变;发作形式以复杂部分性发作为主,也可以继发全面性发作。致痫灶位于枕叶内侧面2例,背外侧面7例,其中致痫灶位于枕叶与顶叶的临界区1例,枕叶与颞叶的临界区或累及颞叶后部4例。术后随访1年以上,按照Engel's术后效果分级:Ⅰ级5例,Ⅱ级2例,Ⅲ级1例,Ⅳ级1例。结论:视觉先兆的出现常常提示致痫灶位于枕叶,MRI检查以及发作初始期头和眼向一侧偏转等症状学特点均有较高的定侧定位价值。当其他方法定位致痫灶较困难时,应用颅内电极记录有助于定位。     

长程颅内电极记录定位致痫灶的效果分析

目的 讨论应用颅内埋藏电极进行长程视频脑电(Video-EEG)监测，对于致痫灶的定位作用。方法 应用立体定向技术，向颅内可疑部位植入深部电极和／或硬膜下条状电极。采用DaVinci系统，进行长程视频脑电监测，记录发作间期及发作期EEG变化，确定癫痫起源部位。在皮层电极脑电图(ECoG)监测下，手术切除致痫灶或行立体定向毁损术。结果 本组17例患者颅内电极埋藏时间4～17天，平均9天。各例均记录到明确的发作间期异常放电和／或发作期EEG变化。手术切除致痫灶16例(联合胼胝体切开术1例)；行双侧杏仁核毁损术1例。术后复查Vidoo-EEG，显示痫性放电基本消失15例，改善2例(集中于手术对侧1例)。按照Engel术后效果分级：Ⅰ级15例，Ⅲ级1例，Ⅳ级1例。所有病例均未出现因长时间埋藏颅内电极引起的并发症。结论 在致痫灶定位困难的难治性癫痫患者中，应用埋藏式颅内深部电极和／或硬膜下条状电极，进行长程颅内电极记录，可以精确定位致痫灶，可改变外科治疗计划，从而提高了癫痫的治愈率及手术成功率。     

额叶癫痫的特点及手术治疗

目的 :分析额叶癫痫的临床特征、发作期及发作间期脑电图特点 ,探讨额叶癫痫手术治疗。方法 :应用视频脑电图对 9例额叶癫痫患者进行长程监测 ,并对其中 6例记录颅内脑电图。分析癫痫发作的临床表现及脑电图特点 ,定位致痫灶 ,行手术切除。结果 :额叶癫痫的发作特点为 :发作频繁而短暂 ,以睡眠期发作为主 ,常见过度运动 ,姿势性强直 ,发声等发作症状。发作期可见棘波节律 ,广泛低幅快活动 ,节律性慢波等特征性脑电活动。颅内电极记录可清晰显示异常脑电活动的发作起源及扩散情况 ,有助于定位致痫灶。手术切除病灶及致痫灶 ,效果满意。结论 :额叶癫痫是一组具有特征性的癫痫综合征 ,颅内电极记录有助于揭示其脑电活动变化。对于难治疗性额叶癫痫 ,准确定位致痫灶是手术成功的关键。     

颅内电极监测技术在癫痫手术中的应用

目的探讨颅内电极监测技术在难治性癫痫外科治疗中的应用价值。方法对头皮脑电图及影像学等非侵袭性检查难以确定致痫灶或致痫灶与重要功能区关系密切的51例难治性癫痫患者,行颅内电极埋置术,长程视频脑电图监测确定致痫灶,并行脑皮层电刺激功能区测定,再次手术切除致痫灶。结果术后致痫灶切除效果按Engel分级：I级32例,Ⅱ级13例,Ⅲ级5例,Ⅳ级1例。术后发生头皮愈合不良3例,延长住院时间后治愈。无脑脊液漏及永久性神经功能缺失发生。结论颅内电极监测可以精确定位致痫灶,皮层电刺激术对脑功能区定位可靠、方便,故对于采用非侵袭性检查不能明确致痫灶或致痫灶与重要功能区关系密切的难治性癫痫患者,颅内电极监测结合皮层电刺激术可以提高其治愈率,并有效降低并发症发生率。     

颅内电极脑电图监测对癫痫致痫灶的定位作用

目的探讨颅内电极脑电图（EEG）监测对癫痫致痫灶的定位作用。方法对经临床、影像学和常规EEG检查不能确定致痫灶部位的20例难治性颞叶癫痫患者，应用立体定向技术，经双侧颞叶植入硬膜下条状电极进行长时间EEG监测，观察发作期及发作间期EEG变化，结合常规EEG、MRI检查结果对癫痫灶进行综合定位；术后随访，评估致痫灶定位的准确性。结果20例患者颅内电极埋藏时间为1—5d，每例监测到／〉2次临床发作并记录发作间期和发作期的异常放电活动。20例患者发作期颅内电极EEG均能准确定位，15例致痫灶发作间期与发作期一致，2例发作间期为双侧棘波，3例发作间期定位与发作期不一致。术后按Engel疗效分级：发作消失13例（65％），显著改善3例（15％），良好3例（15％），无效1例（5％）。未出现因颅内电极安置所致的并发症。结论颅内电极EEG监测可为癫痫手术治疗提供可靠的病灶定位依据。     

内侧额叶癫痫发作的临床特征分析

目的 分析内侧额叶癫痫发作的临床特征。方法 回顾性分析10例经手术证实的内侧额叶起源的癫痫患者129次临床发作症状，脑电图表现，致痫灶定位及手术结果等临床资料。结果 内侧额叶癫痫发作的常见形式包括：过度运动发作、姿势性强直发作、额叶失神发作等，多在夜间发作，持续时间较短暂。10例均应用颅内电极进行长程记录定位致痫灶。致痫灶位于辅助运动区2例，内侧额回4例，额极1例，眶额区1例，扣带回1例，扣带回及额上回1例。按照Engel术后效果进行分级，Ⅰ级3例，Ⅱ级2例，Ⅲ级3例，2例随访时间未满1年。结论 内侧额叶癫痫发作具有一定的特征性。普通头皮脑电图定位致痫灶常较困难，需要应用颅内电极。手术切除致痫灶效果较满意。     

颅内电极埋藏在Lennox-Gastaut综合症中的应用(附10例临床分析)

目的探讨颅内电极埋藏术后进行视频脑电图评估在癫痫外科手术致痫灶定位困难的Lennox-Gastaut综合症中的使用。方法收集10例Lennox-Gastaut综合症致痫灶定位困难的患者,向颅内硬膜下植入条状电极,术后进行视频脑电图评估,记录发作间歇期及发作期脑电图变化,确定癫痫病灶的起始区,通过手术方式切除致痫灶。结果本组10例患者埋藏时间为2～7天,平均4天,均记录到间歇期及发作期脑电图情况。根据脑电图结果,行脑叶切除及胼胝体切开。术后按照Engel评分I级4例,II级2例,III级2例,IV级2例。所有病例均未出现埋藏电极引起的严重并发症。结论在致痫灶定位困难的Lennox-Gastaut综合症中,采用颅内电极埋藏进行视频脑电图检测,可以较准确定位主要致痫灶,从而提高Lennox-Gastaut综合症外科治疗有效率。     

额叶癫癎发作的癫癎灶定位

目的 通过分析40例额叶癫痫发作患者术前定位的临床资料，探讨额叶癫痫发作的癫痫灶综合定位方法。方法 应用临床发作症状评估、MRI／CT扫描、单光子发射计算机体层摄影术(SPECT)检查、长程视频脑电图监测以及颅内电极记录等方法综合定位额叶癫痫患者的癫痫灶。结果 应用非侵袭性检查可以为45．0％的患者进行额叶癫痫灶定位；结合颅内脑电图长程记录，癫痫灶定位率可达90．0％；当影像学检查阴性时，78．9％的患者可以定位癫痫灶。结论 应用临床发作症状学评估、影像学检查、长程视频脑电图监测以及颅内脑电图长程记录相结合的综合定位方法，可以显著提高额叶癫痫发作的癫痫灶定位效果。     

Musicogenic seizures can arise from multiple temporal lobe foci: intracranial EEG analyses of three patients

PURPOSE: To determine the ictal-onset zone of musicogenic seizures by using intracranial EEG monitoring. METHODS: Musicogenic seizures in three patients with medically intractable musicogenic epilepsy were first localized by using noninvasive methods including, in one patient, ictal magnetoencephalography (MEG) and magnetic resonance spectroscopy (MRS). The ictal-onset zones in these patients were then further localized using by intracranial EEG monitoring, and the outcomes of the two patients who underwent epilepsy surgery were determined. RESULTS: Patient 1's musicogenic seizures localized to the right lateral temporal lobe, patient 2's originated in the right mesial temporal lobe, and patient 3's arose independently from both mesial temporal lobes. Patients 1 and 2 underwent resective epilepsy surgery and are seizure free (Engel class I). CONCLUSIONS: Musicogenic epilepsy is a heterogeneous syndrome with seizures that can arise from multiple temporal lobe foci. Patients with medically intractable musicogenic epilepsy and with unilateral ictal onset zones may be considered candidates for resective epilepsy surgery.     

Depth Electrode Studies in Temporal Lobe Epilepsy: Relation to Quantitative Magnetic Resonance Imaging and Operative Outcome

Summary: We performed a retrospective study of 30 patients with presumed intractable temporal lobe epilepsy (TLE) who underwent chronic intracranial EEG monitoring (CIEM). Multicontact depth electrodes were stereotactically implanted through the medial occipital lobe into amygdala and hippocampus. All patients had previously undergone extracranial ictal EEG monitoring that proved inadequate to localize the epileptogenic zone. No morbidity as associated with CIEM in the 30 patients. Twenty-five patients were shown to have exclusively or predominantly unilateral temporal lobe seizures, and 5 patients had bitemporal seizures without unilateral predominance; 24 patients subsequently underwent an anterotemporal lobe cortical resection. Twenty-one patients have been followed a minimum of 1 year postoperatively. Nine patients (43%) had a class I outcome (seizure-free, auras only, or provoked seizures), 3 patients (14%) had a class I1 outcome (≥95% seizure reduction), 4 patients (19%) had a class III outcome (≥50% seizure reduction); and 5 patients (24%) had a class IV outcome (<50% seizure reduction or no change). A prolonged interhemispheric propagation time (p <0.01) and magnetic resonance imaging (MR1)-identified hippocampal atrophy (p <0.01) correlated with a favorable surgical outcome. Results of this study may prove useful in counseling patients who undergo CIEM before temporal lobe surgery.     

Tailored resections in occipital lobe epilepsy surgery guided by monitoring with subdural electrodes: characteristics and outcome

PURPOSE: Occipital lobe epilepsy is uncommon in epilepsy surgery series and often difficult to assess due to rapid seizure propagation, misleading seizure semiology and confounding interictal epileptiform activity. Ictal recordings with surface electrodes may not define properly the seizure onset zone in surgical evaluation for intractable occipital epilepsy. Specially in dysplastic lesions, the extension of the epileptogenic zone is not well defined by neuroimaging techniques, therefore, implantation of intracranial electrodes is often indicated. In this study we present our experience with individually tailored resections of occipital lobe epileptic foci guided by monitoring with subdural electrodes. METHODS: Data from interictal and ictal surface and intracranial recordings, neuroimaging, surgical treatment, pathology and outcome of seven patients are presented. RESULTS: The most common seizure type (6/7 patients) was complex partial with temporal lobe semiology, five patients experienced visual auras as part of their complex partial seizures or as separate simple partial seizures. Two patients had seizures suggesting supplementary motor area involvement. One patient had temporal as well as frontal seizure propagation. Neuroimaging showed lesions in 6/7 patients. Pathological studies revealed cortical dysplasia and tumors as the most common causes. Intracranial recordings (6/7 patients) revealed focal onset in 2 patients, regional onset in 2, and diffuse onset in 2. Surgery was performed according to intracranial recordings restricting resections in cases with focal seizure onset (even in large dysplastic lesions) and performing wider resections in patients with regional or diffuse onset. Five of seven patients are seizure free after 12-55 months (mean 24.3). The two remaining patients may be classified as Engel 2b and 3a. CONCLUSIONS: This series of occipital lobe epilepsy surgery shows that, even in patients with cortical dysplasias, restricted resections may have a good outcome and that intracranial monitoring is usually necessary in order to design an individually tailored resection.     

Occipital lobe epilepsy: clinical characteristics, surgical outcome, and role of diagnostic modalities

PURPOSE: To assess the role of various diagnostic modalities, to identify surgical prognostic factors and concordances with presurgical evaluations, and to characterize the clinical features of occipital lobe epilepsy (OLE), we studied 26 patients who were diagnosed as having OLE and underwent epilepsy surgery. METHODS: Diagnoses were established by standard presurgical evaluations, which included magnetic resonance imaging (MRI), fluorodeoxyglucose-positron emission tomography (FDG-PET), ictal single-photon emission computed tomography (SPECT), scalp video-EEG monitoring, and intracranial EEG monitoring. After epilepsy surgery, patients were followed up for >2 years. RESULTS: Sixteen (61.5%) of the 26 became seizure free after surgery, and another eight patients had a favorable outcome. Sixteen of the 26 patients experienced a type of visual aura (i.e., visual hallucination, visual illusion, blindness, or a field defect). Nine patients had both automotor seizures and secondary generalized tonic-clonic seizures at different times. Interictal EEG showed correctly localizing spikes in 10 of the 16 patients who became seizure free, and in three of the 10 non-seizure-free patients. MRI correctly localized the lesion in seven of these 16 seizure-free patients, and in three of the 10 non-seizure-free patients. FDG-PET correctly localized the lesion in eight of the 16 seizure-free patients, and in three of nine non-seizure-free patients. Ictal SPECT was performed in 19 patients and correctly localized the lesion in only three of 12 seizure-free patients, and in four of seven non-seizure-free patients. Ictal EEG correctly localized the lesion in 13 of the 16 seizure-free patients, and in five of the 10 non-seizure-free patients. No significant relation was found between the diagnostic accuracy of any modality and surgical outcome. The localizations of epileptogenic zones by these different diagnostic methods were complementary. The concordance of three or more modalities was significantly observed in seizure-free patients (p = 0.042). However, no definite relation was observed between the presence of lateralizing clinical seizure manifestation and surgical outcome (p = 0.108). CONCLUSIONS: Some specific auras indicated an occipital epilepsy onset. Various diagnostic methods can be useful to diagnose OLE, and a greater concordance between presurgical evaluation modalities indicates a better surgical outcome.