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[脑白质病变中的扩散各向异性]

[Diffusion anisotropy in cerebral white matter lesion].

作者信息

Segawa F, Kishibayashi J, Kamada K, Sunohara N, Kinoshita M

机构信息

Fourth Department of Internal Medicine, Toho University Ohashi Hospital, Tokyo, Japan.

出版信息

No To Shinkei. 1994 Aug;46(8):765-70.

PMID:7946633
Abstract

Diffusion MRI studies were performed on 14 patients with diffuse high-signal lesions of the cerebral white matter on T2-weighted MR images. There were two patients with adrenoleukodystrophy, four with dentato-rubro-pallido-luysian atrophy, three with familial spastic paraplegia, two with myotonic dystrophy and three with dementia of unknown origin. In addition, a patient with of Sanfilippo disease and one of the three patients who exhibited dementia of unknown origin were also found to be low-signal in the cerebral cortex T2-weighted MR images. In every case except the last two, diffusion-weighted MR images yielded significantly higher apparent diffusion coefficients perpendicular to nerve fibers in the frontal white matter and the corpus callosum than in the normal controls. The lesions displayed increased diffusion anisotropy, calculated as the ratio of the diffusion coefficient perpendicular to the nerve fibers to the diffusion coefficient parallel to the nerve fibers, i.e., diffusion anisotropy was lost in the white matter, suggesting a demyelinating process in the lesion. In the last two cases, on the other hand, the diffusion coefficient and diffusion anisotropy were within normal range. The white matter lesions in these cases were thought to represent degeneration secondary to the cortical involvement. Thus, it was confirmed that diffusion-weighted MR images, unlike T2-weighted MR images, were confirmed to allow differentiation between at least two types of white matter lesions.

摘要

对14例在T2加权磁共振成像(MR图像)上显示脑白质弥漫性高信号病变的患者进行了扩散加权磁共振成像研究。其中2例患有肾上腺脑白质营养不良,4例患有齿状核-红核-苍白球-路易体萎缩,3例患有家族性痉挛性截瘫,2例患有强直性肌营养不良,3例患有不明原因的痴呆。此外,1例患有Sanfilippo病的患者以及3例不明原因痴呆患者中的1例,在脑皮质T2加权MR图像上也显示为低信号。除最后2例患者外,在每例患者中,扩散加权MR图像显示额叶白质和胼胝体中垂直于神经纤维的表观扩散系数明显高于正常对照组。病变显示扩散各向异性增加,扩散各向异性的计算方法是垂直于神经纤维的扩散系数与平行于神经纤维的扩散系数之比,即白质中扩散各向异性丧失,提示病变存在脱髓鞘过程。另一方面,在最后2例患者中,扩散系数和扩散各向异性在正常范围内。这些病例中的白质病变被认为是继发于皮质受累的变性。因此,证实了与T2加权MR图像不同,扩散加权MR图像能够区分至少两种类型的白质病变。

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