Nishimura M, Mito T, Takashima S, Kawahara H, Tanaka J, Nakamura H, Kisa T
Neuropediatrics. 1987 May;18(2):91-5. doi: 10.1055/s-2008-1052460.
A 4-year-old girl with multiple system degeneration and retinal degeneration was presented. There was onset of an ataxic gait at two years and rapid progression of retinal degeneration, myoclonus and cranial nerve palsy. Neuropathological examination revealed severe degeneration of the cerebellar cortex and the pathways of auditory and deep sensation, as well as degeneration of the cerebellar efferent fibers, the striatonigral system, the cerebellar afferent fiber system and lower motor neurons. Cases of young children with spinocerebellar degeneration have been reported in several families of olivopontocerebellar atrophy (OPCA), but degenerative changes in our case were more widespread than those in OPCA cases. The multiple system lesions in the central nervous system and retina of this child are different from those of any other previously reported cases.
本文报告了一名患有多系统退化和视网膜退化的4岁女孩。患儿两岁时出现共济失调步态,并伴有视网膜退化、肌阵挛和颅神经麻痹的快速进展。神经病理学检查显示,小脑皮质以及听觉和深部感觉传导通路严重退化,同时小脑传出纤维、纹状体黑质系统、小脑传入纤维系统和下运动神经元也发生退化。在橄榄体脑桥小脑萎缩(OPCA)的几个家族中曾报道过幼儿患脊髓小脑退化的病例,但我们病例中的退化性改变比OPCA病例更为广泛。该患儿中枢神经系统和视网膜的多系统病变与之前报道的任何病例均不同。