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一名4岁男孩的弥漫性中枢性髓鞘病(消失性白质病)

Myelinopathia centralis diffusa (vanishing white matter disease) in a four-year-old boy.

作者信息

Sinzig J K, Seitz A, Brockmann K, König S

机构信息

University Children's Hospital, Mannheim, Germany.

出版信息

J Neuroradiol. 2004 Mar;31(2):142-4. doi: 10.1016/s0150-9861(04)96981-7.

Abstract

A four-year-old boy presented with moderate ataxia triggered by a minor head trauma several weeks ago. Discrepantly severe signal changes of cerebral white matter with almost CSF-isointense signal on all pulse sequences were detected at cranial MRI. Localized proton MR spectroscopy of cerebral white matter demonstrated an even decrease of all metabolites. Glycine was found elevated in CSF. This pattern of clinical history, MR imaging and spectroscopy features and elevated glycine in CSF is characteristic for a novel entity amongst the leukoencephalopathies of childhood. It was originally termed "myelinopathia centralis diffusa" and renamed "vanishing white matter disease" later.

摘要

一名4岁男孩几周前因轻微头部外伤引发中度共济失调。头颅MRI检查发现脑白质信号改变严重,所有脉冲序列上几乎呈脑脊液等信号。脑白质局部质子磁共振波谱显示所有代谢物均有均匀减少。脑脊液中甘氨酸水平升高。这种临床病史、磁共振成像和波谱特征以及脑脊液中甘氨酸升高的模式是儿童白质脑病中一种新疾病的特征。它最初被称为“弥漫性中枢性髓鞘病”,后来更名为“消失性白质病”。

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