Fazekas G, Kleinert G, Schmidt R, Offenbacher H, Kapeller P, Fazekas F
Universitätsklinik für Neurologie, Graz,
Wien Med Wochenschr. 1996;146(9-10):204-6.
We compared the magnetic resonance imaging results of 15 patients suffering from amyotrophic lateral sclerosis (ALS) with those of 30 age-matched controls to search for disease specific cerebral abnormalities. Symmetric hyperintensity along the corticospinal tract on the proton density spin-echo sequence was exclusively found in 4 ALS patients. It was associated with younger age, rapid disease progression and evolution of symptoms starting in the lower extremities. Signal loss of the motor cortex on T2-weighted images was frequently seen in ALS (9 patients) but was also observed in controls. As MRI is capable of providing direct evidence for ALS besides excluding other diseases it should be included in the diagnostic work-up of these patients.
我们将15例肌萎缩侧索硬化症(ALS)患者的磁共振成像结果与30例年龄匹配的对照者进行比较,以寻找疾病特异性的脑部异常。仅在4例ALS患者中发现质子密度自旋回波序列上沿皮质脊髓束的对称性高信号。它与较年轻的年龄、疾病快速进展以及始于下肢的症状演变有关。T2加权图像上运动皮质的信号丢失在ALS患者中很常见(9例),但在对照者中也有观察到。由于MRI除了能排除其他疾病外,还能够为ALS提供直接证据,因此应将其纳入这些患者的诊断检查中。