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米勒-迪克综合征的急性脑病伴双相发作和后期弥散受限的不典型表现。

Unusual presentation of acute encephalopathy with biphasic seizures and late reduced diffusion in Miller-Dieker syndrome.

机构信息

Department of Pediatrics, Nagoya City University West Medical Center, Nagoya, Aichi, Japan

Department of Radiology, Nagoya City University West Medical Center, Nagoya, Aichi, Japan.

出版信息

BMJ Case Rep. 2022 Mar 16;15(3):e248190. doi: 10.1136/bcr-2021-248190.

Abstract

Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is a unique subtype of acute encephalopathy that occurs in children. A girl aged 2 years and 8 months with Miller-Dieker syndrome (MDS) was admitted for status epilepticus and high fever. Brain MRI performed on the third day postadmission showed abnormally high intensities in the subcortical white matter on diffusion-weighted images. Acute encephalitis/encephalopathy was diagnosed based on the electroencephalography (EEG) findings of diffuse high-voltage delta waves. Six days postadmission, frequent apnoeic episodes were observed, with oxygen desaturation due to cluster seizures. Subclinical seizures were found on amplitude-integrated EEG (aEEG). The disturbance of consciousness was difficult to recognise because of severe developmental disabilities due to MDS. EEG aids in the evaluation of consciousness, and aEEG can be helpful in monitoring and controlling subclinical seizures in the biphasic phase of AESD, especially in patients with underlying neurological disorders.

摘要

急性伴双相抽搐和后期弥散受限脑病(AESD)是一种儿童特有的急性脑病的独特亚型。一名 2 岁 8 个月大的患有 Miller-Dieker 综合征(MDS)的女孩因癫痫持续状态和高热入院。入院后第三天的脑部 MRI 显示弥散加权图像上皮质下白质的异常高信号。根据脑电图(EEG)表现为弥漫性高电压δ波,诊断为急性脑炎/脑病。入院后第 6 天,观察到频繁的呼吸暂停发作,由于簇状发作导致血氧饱和度下降。振幅整合脑电图(aEEG)发现亚临床发作。由于 MDS 导致的严重发育障碍,意识障碍难以识别。EEG 有助于评估意识,aEEG 可有助于监测和控制 AESD 双相期的亚临床发作,特别是在有潜在神经障碍的患者中。

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Two newly proposed infectious encephalitis/encephalopathy syndromes.两种新提出的感染性脑炎/脑病综合征。
Brain Dev. 2009 Aug;31(7):521-8. doi: 10.1016/j.braindev.2009.02.012. Epub 2009 Mar 31.

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