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内镜经脑室“由内向外”胼胝体切开术:病例说明

Endoscopic transventricular "inside-out" corpus callosotomy: illustrative case.

作者信息

Baumgartner Michael E, Atallah Elias, Galligan Kathleen, McDonnell Pamela, Kennedy Benjamin C

机构信息

Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

Department of Neurological Surgery, Thomas Jefferson University, Philadelphia, Pennsylvania.

出版信息

J Neurosurg Case Lessons. 2024 Aug 26;8(9). doi: 10.3171/CASE24160.

Abstract

BACKGROUND

Tonic and atonic "drop attack" seizures are a classic and morbid semiology in Lennox-Gastaut syndrome, resulting in frequent injuries and emergency room visits, in addition to neurocognitive sequelae. Recent years have seen a growing interest in less invasive techniques for performing the classic surgical treatment for drop attacks in Lennox-Gastaut syndrome, that is, corpus callosotomy.

OBSERVATIONS

A 5-year-old boy with Lennox-Gastaut syndrome presented for surgical evaluation. He experienced up to 20 daily tonic seizures despite multiple antiseizure medications. Preoperative imaging revealed highly abnormal anatomy with severe ventriculomegaly and thinning of the cortex and corpus callosum. Open microsurgery or an interhemispheric bimanual endoscopic approach to corpus callosotomy posed a risk for ventricular collapse and subdural hematoma, and the corpus callosum was too thin for laser ablation. A fully endoscopic transventricular "inside-out" complete corpus callosotomy was performed through a 7-mm burr hole via a single working channel without intraoperative complications. The patient continues to experience daily seizures but with a reduced frequency and intensity and a family-reported increased quality of life.

LESSONS

In cases of drug-resistant tonic and atonic seizures associated with ventriculomegaly, a fully endoscopic transventricular complete corpus callosotomy can be performed safely, potentially limiting the risk of ventricular collapse and subdural bleeding. https://thejns.org/doi/10.3171/CASE24160.

摘要

背景

强直性和失张力性“跌倒发作”癫痫是Lennox-Gastaut综合征的一种典型且严重的症状学表现,除了神经认知后遗症外,还会导致频繁受伤和急诊就诊。近年来,人们对采用侵入性较小的技术来进行Lennox-Gastaut综合征跌倒发作的经典手术治疗(即胼胝体切开术)的兴趣日益浓厚。

观察结果

一名患有Lennox-Gastaut综合征的5岁男孩接受手术评估。尽管使用了多种抗癫痫药物,但他每天仍发作多达20次强直性癫痫。术前影像学检查显示解剖结构高度异常,伴有严重的脑室扩大以及皮质和胼胝体变薄。采用开放式显微手术或经半球间双手操作的内镜方法进行胼胝体切开术存在脑室塌陷和硬膜下血肿的风险,而且胼胝体过薄无法进行激光消融。通过一个7毫米的骨孔,经单一工作通道进行了全内镜经脑室“由内向外”完全胼胝体切开术,术中无并发症。该患者仍有每日癫痫发作,但发作频率和强度降低,据家属报告生活质量有所提高。

经验教训

在伴有脑室扩大的耐药性强直性和失张力性癫痫病例中,可以安全地进行全内镜经脑室完全胼胝体切开术,这可能会降低脑室塌陷和硬膜下出血的风险。https://thejns.org/doi/10.3171/CASE24160

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/875f/11373692/d6adaea767b4/CASE24160_figure_1.jpg

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