Konishi Y, Kamoshita S
Acta Neuropathol. 1975;31(3):267-70. doi: 10.1007/BF00684566.
A girl aged 8 years and 10 months at death had shown signs of a slowly progressive neurological disease with onset in early infancy. The main clinical features were nystagmus, spastic paraplegia, amd mental deterioration. Pathological examination of the brain showed severe demyelination with perivascular preservation of mylein islands, presenting a tigroid pattern. The patient is the second case of classical Pelizaeus-Merzbacher's disease in Japan proven by autopsy.
一名8岁10个月大的女童在死亡时已表现出在婴儿早期发病的缓慢进展性神经疾病迹象。主要临床特征为眼球震颤、痉挛性截瘫和智力衰退。脑部病理检查显示严重脱髓鞘,血管周围有髓鞘岛保留,呈现虎斑样图案。该患者是日本经尸检证实的第二例典型佩利措伊斯-默茨巴赫病病例。