Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan; Brain & Mind Research Center, Nagoya University, Nagoya, Japan.
Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan; Brain & Mind Research Center, Nagoya University, Nagoya, Japan.
Brain Dev. 2024 Oct;46(9):302-307. doi: 10.1016/j.braindev.2024.07.003. Epub 2024 Aug 1.
Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) develops along with status epilepticus and widespread subcortical white matter edema. We aimed to evaluate the epileptic foci and networks in two patients with epilepsy after AESD using simultaneous electroencephalography and functional magnetic resonance imaging (EEG-fMRI).
Statistically significant blood oxygen level-dependent (BOLD) responses related to interictal epileptiform discharges (IEDs) were analyzed using an event-related design of hemodynamic response functions with multiple peaks.
Patient 1 developed focal seizures at age 10 years, one year after AESD onset. Positive BOLD changes were observed in the bilateral frontotemporal lobes, left parietal lobe, and left insula. BOLD changes were also observed in the subcortical structures. Patient 2 developed epileptic spasms at age two years, one month after AESD onset. Following total corpus callosotomy (CC) at age three years, the epileptic spasms resolved, and neurodevelopmental improvement was observed. Before CC, positive BOLD changes were observed bilaterally in the frontotemporal lobes. BOLD changes were also observed in the subcortical structures. After CC, the positive BOLD changes were localized in the temporal lobe ipsilateral to the IEDs, and the negative BOLD changes were mainly in the cortex and subcortical structures of the hemisphere ipsilateral to IEDs.
EEG-fMRI revealed multiple epileptic foci and extensive epileptic networks, including subcortical structures in two cases with post-AESD epilepsy. CC may be effective in disconnecting the bilaterally synchronous epileptic networks of epileptic spasms after AESD, and pre-and post-operative changes in EEG-fMRI may reflect improvements in epileptic symptoms.
急性伴癫痫发作和后期弥散受限的脑病(AESD)与癫痫持续状态和广泛的皮质下白质水肿一起发展。我们旨在使用同时进行的脑电图和功能磁共振成像(EEG-fMRI)评估 AESD 后两名癫痫患者的癫痫灶和网络。
使用具有多个峰的血流动力学反应函数的事件相关设计分析与间发性癫痫样放电(IED)相关的统计上显著的血氧水平依赖性(BOLD)反应。
患者 1 在 AESD 发病一年后 10 岁时出现局灶性癫痫发作。在双侧额颞叶、左顶叶和左岛叶观察到阳性 BOLD 变化。BOLD 变化也在皮质下结构中观察到。患者 2 在 AESD 发病一个月后两岁时出现癫痫性痉挛。在三岁时进行全胼胝体切开术(CC)后,癫痫性痉挛得到缓解,神经发育得到改善。在 CC 之前,双侧额颞叶观察到阳性 BOLD 变化。BOLD 变化也在皮质下结构中观察到。在 CC 之后,阳性 BOLD 变化定位于 IED 同侧的颞叶,而阴性 BOLD 变化主要在 IED 同侧半球的皮质和皮质下结构中。
EEG-fMRI 显示了两个 AESD 后癫痫病例中的多个癫痫灶和广泛的癫痫网络,包括皮质下结构。CC 可能有效地阻断 AESD 后癫痫性痉挛的双侧同步癫痫网络,并且 EEG-fMRI 的术前和术后变化可能反映了癫痫症状的改善。