Andreadou E, Sgouropoulos P, Varelas P, Gouliamos A, Papageorgiou C
Eginition Hospital, Athens, Greece.
Neuroradiology. 1998 May;40(5):298-302. doi: 10.1007/s002340050588.
MRI was performed in 32 patients with motor neurone disease (26 men and 6 women, aged 40-77 years) and in a control group of 21 subjects. Of the patients studied, 19 had definite and 11 probable amyotrophic lateral sclerosis (ALS) and two had progressive bulbar palsy. In 10 patients there were asymmetrical bilateral foci of increased signal intensity on proton-density and T2-weighted images, confined to the white matter. Two patients had only cortical frontal atrophy and slightly increased ventricular size, whereas 20 had normal MRI. The focal lesions were not confined to corticospinal tracts, but were also observed in subcortical frontal areas. While the lesions along the corticospinal tracts correspond to pyramidal tract degeneration, the subcortical foci correlate with degeneration of the frontal bundles and indicate generalised involvement of the central nervous system.
对32例运动神经元病患者(26例男性,6例女性,年龄40 - 77岁)和21名对照者进行了磁共振成像(MRI)检查。在研究的患者中,19例患有明确的肌萎缩侧索硬化症(ALS),11例可能患有ALS,2例患有进行性延髓麻痹。10例患者在质子密度和T2加权图像上有不对称的双侧白质信号强度增加灶。2例患者仅有皮质额叶萎缩和脑室轻度增大,而20例患者MRI正常。局灶性病变不仅局限于皮质脊髓束,在皮质下额叶区域也有发现。虽然沿皮质脊髓束的病变对应于锥体束变性,但皮质下病灶与额叶束变性相关,提示中枢神经系统的广泛受累。