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进展性海马硬化的磁共振成像证据:一例报告

Magnetic resonance imaging evidence of hippocampal sclerosis in progression: a case report.

作者信息

Nohria V, Lee N, Tien R D, Heinz E R, Smith J S, DeLong G R, Skeen M B, Resnick T J, Crain B, Lewis D V

机构信息

Department of Pediatrics, Duke University Medical Center, Durham, North Carolina 27710.

出版信息

Epilepsia. 1994 Nov-Dec;35(6):1332-6. doi: 10.1111/j.1528-1157.1994.tb01807.x.

Abstract

A 32-month-old child presented in status epilepticus (SE) involving the left side of the body. Fast spin-echo magnetic resonance imaging (FSE-MRI) with hippocampal volumetry performed < or = 24 h after the seizure showed increased T2 signal of the right hippocampus, but no atrophy. Complex partial seizures (CPS) appeared at age 33 months, and three more episodes of SE occurred between 33 and 37 months of age. Follow-up FSE-MRI at 34 and at 45 months of age demonstrated progressive hippocampal atrophy with resolution of the increased T2 signal. Her CPS became intractable and, at age 51 months, she underwent right temporal lobectomy. In the ensuing 5 months, she has had only one major motor seizure. This case demonstrates that acute increased hippocampal T2 signal intensity can occur soon after SE and hippocampal sclerosis (HS) may become evident within months in the setting of recurrent early childhood SE. This observation may support the hypothesis that early childhood SE can lead to HS. Furthermore, this case suggests that years of temporal lobe CPS may not be necessary for development of HS.

摘要

一名32个月大的儿童出现累及身体左侧的癫痫持续状态(SE)。癫痫发作后≤24小时进行的带有海马体积测量的快速自旋回波磁共振成像(FSE-MRI)显示右侧海马T2信号增强,但无萎缩。33个月大时出现复杂部分性发作(CPS),在33至37个月龄之间又发生了3次SE发作。34个月和45个月龄时的随访FSE-MRI显示海马进行性萎缩,T2信号增强消失。她的CPS变得难以控制,51个月大时接受了右侧颞叶切除术。在随后的5个月里,她仅发生了一次主要的运动性癫痫发作。该病例表明,SE后不久海马T2信号强度可能急性增加,在复发性儿童早期SE的情况下,海马硬化(HS)可能在数月内变得明显。这一观察结果可能支持儿童早期SE可导致HS的假说。此外,该病例表明,HS的发展可能不需要数年的颞叶CPS。

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