Tanabe Y, Iai M, Ishii M, Tamai K, Maemoto T, Ooe K, Takashima S
Division of Neurology, Chiba Children's Hospital, Japan.
Neurology. 1993 Jan;43(1):110-3. doi: 10.1212/wnl.43.1_part_1.110.
We used MRI to investigate the brains of four children ranging from 3 to 10 years of age with infantile neuroaxonal dystrophy. T2-weighted imaging revealed characteristic findings of marked cerebellar atrophy and diffuse hyperintensity of the cerebellar cortex. At autopsy, one child had extensive astrogliosis and neuronal loss with shrinkage of the cerebellar cortex, in addition to typical widespread changes of neuroaxonal dystrophy. The characteristic hyperintensity of the cerebellar cortex on T2-weighted imaging probably is secondary to the extensive gliosis and shrinkage of the cerebellar cortex. These cerebellar findings on MRI may permit early diagnosis of infantile neuroaxonal dystrophy.
我们使用磁共振成像(MRI)对4名年龄在3至10岁之间患有婴儿型神经轴索营养不良的儿童的大脑进行了研究。T2加权成像显示出明显的小脑萎缩和小脑皮质弥漫性高信号等特征性表现。尸检时,除了典型的广泛的神经轴索营养不良改变外,一名儿童还出现了广泛的星形胶质细胞增生、神经元丢失以及小脑皮质萎缩。T2加权成像上小脑皮质特征性的高信号可能继发于小脑皮质广泛的胶质细胞增生和萎缩。MRI上的这些小脑表现可能有助于婴儿型神经轴索营养不良的早期诊断。