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在一个患有齿状核红核苍白球路易体萎缩症的家族中患者的放射学和神经病理学发现。

Radiologic and neuropathologic findings in patients in a family with dentatorubral-pallidoluysian atrophy.

机构信息

Department of Neurology, Tokyo Metropolitan Neurological Hospital, Tokyo, Japan.

出版信息

AJNR Am J Neuroradiol. 2011 Jan;32(1):109-14. doi: 10.3174/ajnr.A2252. Epub 2010 Oct 21.

Abstract

We describe the cases of 2 patients, a father and his son, with DRPLA who underwent MR examinations prior to death and in whom postmortem examinations of the brain were obtained. MR imaging findings had the following features: 1) atrophy of the cerebellum and brain stem were the common findings, 2) high-signal-intensity lesions in the cerebral white matter and brain stem were observed on T2-weighted images in the patient with adult-onset DRPLA, 3) signal-intensity changes in the cerebral white matter were restricted to the periventricular white matter in the patient with juvenile-onset DRPLA, but these changes appear in the advanced stage, and 4) progressive cerebral atrophy was more marked in the patient with juvenile-onset DRPLA. In the patients with DRPLA, the abnormal high signal intensity of the cerebral white matter or brain stem on MR images reflect the loss of myelinated fibers. Cerebral atrophy mainly reflects atrophy of the neuropile.

摘要

我们描述了 2 名患者(父亲和儿子)的病例,他们均患有 DRPLA,在死亡前接受了磁共振成像(MRI)检查,并且获得了脑部的尸检结果。MRI 成像的发现具有以下特征:1)小脑和脑干萎缩是常见的发现;2)成年起病的 DRPLA 患者的 T2 加权图像上可见脑白质和脑干的高信号强度病变;3)少年起病的 DRPLA 患者脑白质的信号强度变化局限于脑室周围白质,但这些变化出现在晚期;4)少年起病的 DRPLA 患者的脑萎缩更为明显。在 DRPLA 患者中,脑白质或脑干的异常高信号强度反映了髓鞘纤维的丧失。脑萎缩主要反映了神经纤维的萎缩。

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本文引用的文献

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A case of late adult-onset dentatorubral-pallidoluysian atrophy mimicking central pontine myelinolysis.
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