结节性硬化症的无创性检查、早期手术和癫痫无发作。
Noninvasive testing, early surgery, and seizure freedom in tuberous sclerosis complex.
机构信息
Division of Pediatric Neurology, Mattel Children's Hospital at UCLA, David Geffen School of Medicine, Los Angeles, CA 90095-1752, USA.
出版信息
Neurology. 2010 Feb 2;74(5):392-8. doi: 10.1212/WNL.0b013e3181ce5d9e.
BACKGROUND
The unambiguous identification of the epileptogenic tubers in individuals with tuberous sclerosis complex (TSC) can be challenging. We assessed whether magnetic source imaging (MSI) and coregistration of (18)fluorodeoxyglucose PET (FDG-PET) with MRI could improve the identification of the epileptogenic regions noninvasively in children with TSC.
METHODS
In addition to standard presurgical evaluation, 28 children with intractable epilepsy from TSC referred from 2000 to 2007 had MSI and FDG-PET/MRI coregistration without extraoperative intracranial EEG.
RESULTS
Based on the concordance of test results, 18 patients with TSC (64%) underwent surgical resection, with the final resection zone confirmed by intraoperative electrocorticography. Twelve patients are seizure free postoperatively (67%), with an average follow-up of 4.1 years. Younger age at surgery and shorter seizure duration were associated with postoperative seizure freedom. Conversely, older age and longer seizure duration were linked with continued seizures postoperatively or prevented surgery because of nonlateralizing or bilateral independent epileptogenic zones. Complete removal of presurgery MSI dipole clusters correlated with postoperative seizure freedom.
CONCLUSIONS
Magnetic source imaging and (18)fluorodeoxyglucose PET/MRI coregistration noninvasively localized the epileptogenic zones in many children with intractable epilepsy from tuberous sclerosis complex (TSC), with 67% seizure free postoperatively. Seizure freedom after surgery correlated with younger age and shorter seizure duration. These findings support the concept that early epilepsy surgery is associated with seizure freedom in children with TSC and intractable epilepsy.
背景
在结节性硬化症(TSC)患者中,明确识别致痫性结节具有一定挑战性。我们评估了磁共振源成像(MSI)和(18)氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)与 MRI 的配准是否能在不进行额外的手术颅内脑电图的情况下,无创性地识别 TSC 患儿的致痫区。
方法
除了标准的术前评估外,2000 年至 2007 年期间,28 名来自 TSC 的耐药性癫痫儿童进行了 MSI 和 FDG-PET/MRI 配准,没有进行手术中的颅内脑电图。
结果
根据测试结果的一致性,18 名 TSC 患者(64%)接受了手术切除,最终的切除区域通过术中皮质电图证实。12 名患者术后无癫痫发作(67%),平均随访 4.1 年。手术时年龄较小和癫痫发作持续时间较短与术后无癫痫发作相关。相反,年龄较大和癫痫发作持续时间较长与术后持续癫痫发作或因非侧化或双侧独立致痫区而无法手术相关。术前 MSI 偶极子簇的完全切除与术后无癫痫发作相关。
结论
磁共振源成像和(18)氟脱氧葡萄糖 PET/MRI 配准无创性定位了许多耐药性癫痫结节性硬化症(TSC)儿童的致痫区,术后 67%的患者无癫痫发作。术后无癫痫发作与手术时年龄较小和癫痫发作持续时间较短相关。这些发现支持这样的观点,即儿童 TSC 和耐药性癫痫患者早期癫痫手术与无癫痫发作相关。
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