Magnetic resonance findings in leucodystrophies and MS.

International MS journal Pub Date : 2009-06-01
P Labauge
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Abstract

White matter diseases are a frequent diagnosis problem in adult patients. They are divided into leucodystrophy, defined by abnormal white matter from the beginning, and leucoencephalopathy, with an initial normal white matter. In addition, two different natures have to be considered: vascular and non-vascular. Vascular diseases are mainly acquired and related to atherosclerosis. Genetic vascular disorders are mostly secondary to Notch3 mutations, defined as cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL). Occurrence of leucoaraiosis and lacunae on T2 sequences, and microbleeds on Gradient Echo sequences, strongly suggest this diagnosis. Some magnetic resonance (MR) patterns can help to identify genetic leucodystrophies, such as childhood ataxia with central nervous system hypomyelination/leucoencephalopathy with vanishing white matter disease (progressive rarefaction and cystic degeneration of the affected white matter, replaced by water); Alexander disease (hypointense signals on T2 sequences involving grey matter, brainstem and cervical cord, with marked atrophy); megalencephalic leucoencephalopathy with subcortical cysts (diffuse, symmetrical white matter lesions, with constant frontoparietal and anterotemporal subcortical cysts); leucoencephalopathy with brainstem and spinal cord involvement and high lactates syndrome (extensive demyelination, involvement of the brainstem, i.e. cerebellar peduncles, intraparenchymal and mesencephalic trigeminal nerves and spinal cord, mainly in the lateral corticospinal tracts and dorsal columns). Half of the genetic adult leucodystrophies remain without any precise diagnosis. This review describes MR in the adult leucoencephalopathies and in multiple sclerosis (MS). The first part will focus on MR patterns of vascular and nonvascular adult leucoencephalopathies, the second part on MR findings in MS and MS-related diseases. Specific MR patterns in both diseases will be summarized and compared.

脑白质营养不良和多发性硬化症的磁共振表现。
白质疾病是成人患者中常见的诊断问题。它们分为白质营养不良症和白质脑病,白质从一开始就异常,白质最初正常。此外,还必须考虑两种不同的性质:血管和非血管。血管疾病主要是获得性的,与动脉粥样硬化有关。遗传性血管疾病大多继发于Notch3突变,定义为大脑常染色体显性动脉病变伴皮层下梗死和白质脑病(CADASIL)。T2序列上出现白质变和腔隙,梯度回声序列上出现微出血,强烈提示这种诊断。一些磁共振(MR)模式可以帮助识别遗传性白质营养不良,如儿童期共济失调伴中枢神经系统髓鞘过浅/白质脑病伴白质消失(受影响的白质进行性稀疏和囊性变性,被水取代);亚历山大病(T2序列低信号累及灰质、脑干和颈髓,伴有明显萎缩);巨脑白质脑病伴皮层下囊肿(弥漫性对称白质病变,常伴额顶叶和前颞叶皮层下囊肿);白质脑病伴脑干和脊髓受累及高乳酸综合征(广泛脱髓鞘,累及脑干,即小脑梗、脑实质内和中脑三叉神经和脊髓,主要累及外侧皮质脊髓束和背柱)。一半的遗传性成人白质营养不良仍然没有任何精确的诊断。本文综述了成人白质脑病和多发性硬化症(MS)的MR。第一部分将集中于血管性和非血管性成人白质脑病的MR模式,第二部分将集中于MS和MS相关疾病的MR发现。将总结和比较两种疾病的特异性MR模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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