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结构磁共振成像在识别结节性硬化症幼儿致痫灶中的应用有限。

Limited utility of structural MRI to identify the epileptogenic zone in young children with tuberous sclerosis.

机构信息

Localization Laboratory, Division of Epilepsy and Clinical Neurophysiology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Department of Radiology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

出版信息

J Neuroimaging. 2022 Sep;32(5):991-1000. doi: 10.1111/jon.13016. Epub 2022 Jun 21.

Abstract

BACKGROUND AND PURPOSE

The success of epilepsy surgery in children with tuberous sclerosis complex (TSC) hinges on identification of the epileptogenic zone (EZ). We studied structural MRI markers of epileptogenic lesions in young children with TSC.

METHODS

We included 26 children with TSC who underwent epilepsy surgery before the age of 3 years at five sites, with 12 months or more follow-up. Two neuroradiologists, blinded to surgical outcome data, reviewed 10 candidate lesions on preoperative MRI for characteristics of the tuber (large affected area, calcification, cyst-like properties) and of focal cortical dysplasia (FCD) features (cortical malformation, gray-white matter junction blurring, transmantle sign). They selected lesions suspect for the EZ based on structural MRI, and reselected after unblinding to seizure onset location on electroencephalography (EEG).

RESULTS

None of the tuber characteristics and FCD features were distinctive for the EZ, indicated by resected lesions in seizure-free children. With structural MRI alone, the EZ was identified out of 10 lesions in 31%, and with addition of EEG data, this increased to 48%. However, rates of identification of resected lesions in non-seizure-free children were similar. Across 251 lesions, interrater agreement was moderate for large size (κ = .60), and fair (κ = .24) for all other features.

CONCLUSIONS

In young children with TSC, the utility of structural MRI features is limited in the identification of the epileptogenic tuber, but improves when combined with EEG data.

摘要

背景与目的

儿童结节性硬化症(TSC)癫痫手术的成功取决于致痫区(EZ)的确定。我们研究了患有 TSC 的幼儿的结构 MRI 致痫病变标志物。

方法

我们纳入了在五个地点接受癫痫手术的 26 名 TSC 患儿,他们的年龄均在 3 岁以下,随访时间为 12 个月或以上。两名神经放射科医生对术前 MRI 上的 10 个候选病变进行了盲法评估,评估内容包括结节(受累面积大、钙化、囊肿样特征)和局灶性皮质发育不良(FCD)特征(皮质畸形、灰白质交界模糊、脑膜贯通征)。他们根据结构 MRI 选择 EZ 可疑病变,并在对脑电图(EEG)上的发作起始位置去盲后重新选择。

结果

在无癫痫发作的儿童中,没有一种结节特征和 FCD 特征可明确提示 EZ,切除的病变提示 EZ 不存在。单独使用结构 MRI,可识别出 10 个病变中的 3 个(31%),而添加 EEG 数据后,这一比例增加到 48%。然而,在非无癫痫发作的儿童中,切除病变的识别率相似。在 251 个病变中,大尺寸的组内一致性为中等(κ=0.60),而其他所有特征的组内一致性为一般(κ=0.24)。

结论

在患有 TSC 的幼儿中,结构 MRI 特征在识别致痫性结节方面的作用有限,但与 EEG 数据结合使用时可提高其识别能力。

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