Department of Neurology, Mayo Clinic, Rochester, Minnesota 55905, USA.
Epilepsia. 2011 Aug;52(8):1522-6. doi: 10.1111/j.1528-1167.2011.03192.x. Epub 2011 Jul 18.
To evaluate long-term seizure outcome in children with epilepsy and a focal or hemispheric neuroimaging abnormality.
All children (<18 years and residing in Olmsted County, Minnesota) with new-onset epilepsy diagnosed between 1980 and 2004 and a single focal lesion on neuroimaging were identified by review of the Rochester Epidemiologic Project database. Outcomes were divided into three categories: (1) seizure freedom for 1 or more years at last follow-up, (2) ongoing seizures but not medically intractable epilepsy, and (3) medically intractable epilepsy or undergoing epilepsy surgery. We also evaluated the proportion who achieved seizure control without surgical intervention and whether lesion type predicted intractability.
Of the 359 children with newly diagnosed epilepsy, 37 (10%) had a focal or hemispheric lesion on neuroimaging. Median age of diagnosis was 89 months (25th percentile 26 months, 75th percentile 142 months) and at follow-up was 137 months (25th percentile 95 months, 75th percentile 211 months). Eighty-three percent of children with malformations of cortical development, 67% with mesial temporal sclerosis, 33% with encephalomalacia, and 50% with vascular malformations had intractable epilepsy at follow-up or underwent resective surgery for medically intractable epilepsy. Among the different etiologies, presence of encephalomalacia predicted the lowest likelihood of medical intractability or undergoing surgery (p < 0.01). At final follow-up, 24 (65%) of our entire cohort was seizure free. Following surgery, seizure freedom was achieved in 80% with mesial temporal sclerosis, 67% with encephalomalacia, 67% with vascular malformation, and 50% with malformations of cortical development. There was no statistically significant difference between the different etiologies on neuroimaging and seizure freedom after surgery. Twelve children (32%) achieved seizure freedom with medical management alone.
Focal lesions on neuroimaging confer a high risk of medical intractability among children with new-onset epilepsy. However, 32% of this cohort achieved seizure remission with medical management alone, including 58% with encephalomalacia and 33% with mesial temporal sclerosis.
评估有局灶性或半球性神经影像学异常的儿童癫痫的长期癫痫发作结局。
通过审查罗切斯特流行病学项目数据库,确定了 1980 年至 2004 年间新诊断为癫痫且神经影像学检查有单个局灶性病变的所有儿童(年龄<18 岁,居住在明尼苏达州奥姆斯特德县)。结局分为三类:(1)末次随访时至少 1 年无发作,(2)持续发作但非药物难治性癫痫,(3)药物难治性癫痫或正在接受癫痫手术。我们还评估了无手术干预实现癫痫控制的比例,以及病变类型是否预测难治性。
在 359 例新诊断为癫痫的儿童中,37 例(10%)神经影像学检查有局灶性或半球性病变。诊断时的中位年龄为 89 个月(25%分位数为 26 个月,75%分位数为 142 个月),随访时为 137 个月(25%分位数为 95 个月,75%分位数为 211 个月)。皮质发育畸形患儿中 83%、内侧颞叶硬化症患儿中 67%、脑软化症患儿中 33%、血管畸形患儿中 50%在随访时为药物难治性癫痫或接受了手术治疗。在不同病因中,脑软化症的存在预测药物难治性或手术的可能性最低(p<0.01)。在最终随访时,我们整个队列中有 24 例(65%)无发作。手术后,内侧颞叶硬化症的无发作率为 80%,脑软化症为 67%,血管畸形为 67%,皮质发育畸形为 50%。神经影像学不同病因之间手术后无发作的差异无统计学意义。12 例儿童(32%)单独通过药物治疗达到无发作。
神经影像学上的局灶性病变提示新诊断为癫痫的儿童药物难治性风险较高。然而,该队列中有 32%的儿童通过单纯药物治疗实现了癫痫缓解,包括 58%的脑软化症患儿和 33%的内侧颞叶硬化症患儿。