Mascalchi M, Salvi F, Piacentini S, Bartolozzi C
Cattedra di Radiologia, Universita' di Pisa, Italy.
AJR Am J Roentgenol. 1994 Jul;163(1):187-91. doi: 10.2214/ajr.163.1.8010211.
Loss of myelinated fibers and gliosis in the posterior and lateral columns of the spinal cord are histopathologic hallmarks of Friedreich's ataxia. These are accompanied by atrophy of the upper portion of the spinal cord. We performed a study to determine if MR imaging can be used to detect signal changes in the white matter tracts of the cervical spinal cord in these patients.
The cervical spinal cord was imaged with a 0.5-T MR imaging system in 10 patients with Friedreich's ataxia and in 14 patients with cerebellar ataxias, who served as control subjects. In all of them, the examination protocol included sagittal T1-weighted spin-echo images, sagittal short T1 inversion-recovery images, and axial cardiac-gated long TR spin-echo or ungated low-flip-angle (20 degrees) gradient-recalled-echo images from C2 to C6. The anteroposterior diameter of the spinal cord at the level of C3 on axial images was measured on the display console in patients and control subjects. Two observers who did not know the clinical diagnosis were then asked to evaluate hard copies of the entire image set for each subject for possible intramedullary signal abnormalities.
The anteroposterior diameter of the spinal cord was decreased in all but one of the patients with Friedreich's ataxia. Abnormal signal in the posterior or lateral columns of the spinal cord was observed on sagittal and axial images in nine patients with Friedreich's ataxia and in none of the control subjects.
MR images of the cervical spinal cord in patients with Friedreich's ataxia show thinning and intramedullary signal changes in the cervical portion of the spinal cord, consistent with degeneration of posterior and lateral white matter tracts. These MR findings might be helpful for differential diagnosis in patients with progressive ataxia of uncertain clinical type.
脊髓后柱和侧柱中髓鞘纤维的丧失及胶质增生是弗里德赖希共济失调的组织病理学特征。这些特征还伴有脊髓上部萎缩。我们进行了一项研究,以确定磁共振成像(MR成像)是否可用于检测这些患者颈髓白质束中的信号变化。
使用0.5-T MR成像系统对10例弗里德赖希共济失调患者和14例小脑性共济失调患者(作为对照)的颈髓进行成像。所有患者的检查方案包括矢状面T1加权自旋回波图像、矢状面短T1反转恢复图像,以及从C2至C6的轴位面心脏门控长TR自旋回波或非门控低翻转角(20度)梯度回波图像。在患者和对照者的显示控制台测量轴位图像上C3水平脊髓的前后径。然后让两位不了解临床诊断的观察者评估每个受试者的整套图像硬拷贝,以查找可能的髓内信号异常。
除1例弗里德赖希共济失调患者外,其余患者脊髓的前后径均减小。9例弗里德赖希共济失调患者的矢状面和轴位图像上观察到脊髓后柱或侧柱有异常信号,而对照者均未观察到。
弗里德赖希共济失调患者颈髓的MR图像显示脊髓颈段变细及髓内信号变化,这与后柱和侧柱白质束变性一致。这些MR表现可能有助于对临床类型不明的进行性共济失调患者进行鉴别诊断。