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[成人暴发性正染性脑白质营养不良]

[Fulminant orthochromatic leukodystrophy in an adult].

作者信息

Dousset V, Tison F, Vital A, Henry P

机构信息

Service de Neurologie, Hôpital Pellegrin, Bordeaux.

出版信息

Rev Neurol (Paris). 1998 Jun;154(5):415-8.

PMID:9773074
Abstract

A 27-year-old man from Marocco developed a progressive dementia leading within a year to a mutic akinetic state. The course of the disease was also marked by epileptic seizures. MRI revealed diffuse white matter involvement. A frontal white matter brain biopsy was consistent with the diagnosis of orthochromatic leucodystrophy, i.e: presence of sudanophilic lipids and pigmented cells associated with myelin loss. Adult forms of orthochromatic leucodystrophy are very rare. Our case was characterized by a fulminant course.

摘要

一名来自摩洛哥的27岁男子出现进行性痴呆,在一年内发展为多动性缄默状态。疾病过程中还伴有癫痫发作。磁共振成像显示弥漫性白质受累。额叶白质脑活检结果与正染性脑白质营养不良的诊断相符,即存在嗜苏丹脂质和与髓鞘丢失相关的色素细胞。成人型正染性脑白质营养不良非常罕见。我们的病例以暴发性病程为特征。

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