Department of Pediatrics (Neurology), Duke University Medical Center, Durham, North Carolina, USA.
Department of Radiology, Duke University Medical Center, Durham, North Carolina, USA.
Epilepsia. 2024 Jun;65(6):1568-1580. doi: 10.1111/epi.17979. Epub 2024 Apr 12.
This study was undertaken to determine whether hippocampal T2 hyperintensity predicts sequelae of febrile status epilepticus, including hippocampal atrophy, sclerosis, and mesial temporal lobe epilepsy.
Acute magnetic resonance imaging (MRI) was obtained within a mean of 4.4 (SD = 5.5, median = 2.0) days after febrile status on >200 infants with follow-up MRI at approximately 1, 5, and 10 years. Hippocampal size, morphology, and T2 signal intensity were scored visually by neuroradiologists blinded to clinical details. Hippocampal volumetry provided quantitative measurement. Upon the occurrence of two or more unprovoked seizures, subjects were reassessed for epilepsy. Hippocampal volumes were normalized using total brain volumes.
Fourteen of 22 subjects with acute hippocampal T2 hyperintensity returned for follow-up MRI, and 10 developed definite hippocampal sclerosis, which persisted through the 10-year follow-up. Hippocampi appearing normal initially remained normal on visual inspection. However, in subjects with normal-appearing hippocampi, volumetrics indicated that male, but not female, hippocampi were smaller than controls, but increasing hippocampal asymmetry was not seen following febrile status. Forty-four subjects developed epilepsy; six developed mesial temporal lobe epilepsy and, of the six, two had definite, two had equivocal, and two had no hippocampal sclerosis. Only one subject developed mesial temporal epilepsy without initial hyperintensity, and that subject had hippocampal malrotation. Ten-year cumulative incidence of all types of epilepsy, including mesial temporal epilepsy, was highest in subjects with initial T2 hyperintensity and lowest in those with normal signal and no other brain abnormalities.
Hippocampal T2 hyperintensity following febrile status epilepticus predicted hippocampal sclerosis and significant likelihood of mesial temporal lobe epilepsy. Normal hippocampal appearance in the acute postictal MRI was followed by maintained normal appearance, symmetric growth, and lower risk of epilepsy. Volumetric measurement detected mildly decreased hippocampal volume in males with febrile status.
本研究旨在确定海马 T2 高信号是否可预测热性惊厥后癫痫的后遗症,包括海马萎缩、硬化和内侧颞叶癫痫。
在热性惊厥后平均 4.4 天(SD=5.5,中位数=2.0)进行急性磁共振成像(MRI)检查,约 1、5 和 10 年时进行随访 MRI。神经放射科医生在不了解临床细节的情况下对海马的大小、形态和 T2 信号强度进行视觉评分。通过海马容积测量提供定量测量。当出现两次或两次以上无诱因发作时,对患者进行癫痫再评估。使用全脑体积对海马体积进行标准化。
22 例急性海马 T2 高信号患者中有 14 例返回进行随访 MRI,其中 10 例出现明确的海马硬化,且在 10 年随访中持续存在。最初表现为正常的海马在视觉检查中仍保持正常。然而,在海马表现正常的患者中,体积测量显示男性海马小于对照组,但在热性惊厥后并未出现海马不对称性增加,而女性海马则与对照组无差异。44 例患者出现癫痫,6 例出现内侧颞叶癫痫,其中 2 例有明确的、2 例有可疑的、2 例无海马硬化。仅有 1 例出现内侧颞叶癫痫而无初始高信号,且该患者有海马旋转不良。在初始 T2 高信号和信号正常且无其他脑异常的患者中,所有类型癫痫(包括内侧颞叶癫痫)的 10 年累积发生率最高和最低。
热性惊厥后海马 T2 高信号预测海马硬化和内侧颞叶癫痫的高可能性。急性癫痫后 MRI 中海马外观正常,随后保持正常外观、对称生长,癫痫风险较低。体积测量发现热性惊厥男性海马体积轻度减小。