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Surgical Management of Cavernous Malformations Presenting with Drug-Resistant Epilepsy

机译:耐药性癫痫的海绵畸形的外科治疗

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摘要

Cerebral cavernous malformations (CMs) are dynamic lesions characterized by continuous size changes and repeated bleeding. When involving cortical tissue, CMs pose a significant risk for the development of drug-resistant epilepsy, which is thought to be result of an altered neuronal network caused by the lesion itself and its blood degradation products. Preoperative evaluation should comprise a complete seizure history, neurological examination, epilepsy-oriented MRI, EEG, video-EEG, completed with SPECT, PET, functional MRI, and/or invasive monitoring as needed. Radiosurgery shows variable rates of seizure freedom and a high incidence of complications, thus microsurgical resection remains the optimal treatment for CMs presenting with drug-resistant epilepsy. Two thirds of patients reach Engel I class at 3-year follow-up, regardless of lobar location. Those with secondarily generalized seizures, a higher seizure frequency, and generalized abnormalities on preoperative or postoperative EEG, show poorer outcomes, while factors such as gender, duration of epilepsy, lesion size, age, bleeding at the time of surgery, do not correlate consistently with seizure outcome. Electrocorticography and a meticulous removal of all cortical hemosiderin – beyond pure lesionectomy – reduce the risk of symptomatic recurrences.
机译:脑海绵状畸形(CMs)是动态病变,其特征是持续大小变化和反复出血。当涉及皮质组织时,CM对耐药性癫痫的发展构成重大风险,这被认为是由病变本身及其血液降解产物引起的神经元网络改变所致。术前评估应包括完整的癫痫病史,神经系统检查,以癫痫为导向的MRI,EEG,影像脑电图,SPECT,PET,功能性MRI和/或根据需要进行侵入性监测。放射外科手术显示癫痫发作的自由率可变,并发症发生率很高,因此显微外科切除术仍然是出现耐药性癫痫的CM的最佳治疗方法。不管叶的位置如何,三分之二的患者在3年的随访中均达到Engel I级。继发性癫痫发作,较高的癫痫发作频率以及术前或术后脑电图普遍性异常的患者,预后较差,而性别,癫痫病持续时间,病变大小,年龄,手术时出血等因素并不一致癫痫发作的结果。皮质脑电图检查和精心去除所有皮质含铁血黄素-除单纯病变切除术外-减少了症状复发的风险。

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