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儿童局灶性皮质发育不良患者行个体化和标准手术切除的长期癫痫发作结局。

Long-term seizure outcome in pediatric patients with focal cortical dysplasia undergoing tailored and standard surgical resections.

机构信息

Dept. of Epileptology, Medical Center - University of Freiburg, Germany; Faculty of Medicine, University of Freiburg, Germany.

Epilepsy Center Bielefeld, Germany.

出版信息

Seizure. 2018 Nov;62:66-73. doi: 10.1016/j.seizure.2018.09.021. Epub 2018 Sep 26.

DOI:10.1016/j.seizure.2018.09.021
PMID:30296740
Abstract

PURPOSE

Focal cortical dysplasia (FCD) is the major cause of focal intractable epilepsy in childhood. Here we analyze the factors influencing the success of surgical treatment in a large cohort of children with histologically ascertained FCD.

METHOD

A retrospective study of the effects of FCD type, surgical intervention, and age at surgery in a pediatric cohort.

RESULTS

A total of 113 patients (71 male; mean age at surgery 10.3 years; range 0-18) were analyzed; 45 had undergone lesionectomy, 42 lobectomy, 18 multi-lobectomy, and eight hemispherotomy. Complete seizure control (Engel Ia) was achieved in 56% after two years, 52% at five years, and 50% at last follow-up (18-204 months). Resections were more extensive in younger patients (40% of the surgeries affecting more than one lobe in patients aged nine years or younger vs. 22% in patients older than nine years). While resections were more limited in older children, their long-term outcome tended to be superior (42% seizure freedom in patients aged nine years or younger vs. 56% in patients older than nine years). The outcome in FCD I was not significantly inferior to that in FCD II.

CONCLUSIONS

Our data confirm the long-term efficacy of surgery in children with FCD and epilepsy. An earlier age at surgery within this cohort did not predict a better long-term outcome, but it involved less-tailored surgical approaches. The data suggest that in patients with an unclear extent of the dysplastic area, later resections may offer advantages in terms of the precision of surgical-resection planning.

摘要

目的

局灶性皮质发育不良(FCD)是儿童局灶性耐药性癫痫的主要原因。在此,我们分析了在一大群经组织学证实的 FCD 儿童中,影响手术治疗成功的因素。

方法

对儿科队列中 FCD 类型、手术干预和手术时年龄的影响进行回顾性研究。

结果

共分析了 113 例患儿(71 例男性;手术时平均年龄 10.3 岁;范围 0-18 岁);45 例行病灶切除术,42 例行叶切除术,18 例行多叶切除术,8 例行半脑切除术。术后两年完全控制发作(Engel Ia)的比例为 56%,五年为 52%,最后一次随访(18-204 个月)为 50%。在年龄较小的患者中,切除范围较广(9 岁或以下的患者中有 40%的手术影响了一个以上的脑叶,而 9 岁以上的患者中只有 22%)。虽然大龄儿童的切除范围较小,但他们的长期预后往往更好(9 岁或以下的患者中有 42%无发作,而 9 岁以上的患者中有 56%)。FCD I 的结果并不明显劣于 FCD II。

结论

我们的数据证实了手术治疗 FCD 伴癫痫儿童的长期疗效。在本队列中,手术年龄较早并不预示着更好的长期预后,但手术方法也不太适合。数据表明,对于病变区范围不明确的患者,延迟切除可能在手术切除规划的精确性方面具有优势。

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