Harada K, Krucke W, Mancardi J L, Mandybur T I
Max Planck Institute for Brain Research, Frankfurt am Main, West Germany.
Neurology. 1988 Jan;38(1):55-9. doi: 10.1212/wnl.38.1.55.
We present a case of infantile leukodystrophy with some sudanophilic features. A normally developed male infant did well until age 15 months. Then he had episodes of myoclonus, reversal of intellectual development, rigidity with decerebrate posturing and epilepsy, which became severe. He died at age 7 years, 10 months. On autopsy, the brain was normally developed, but there was severe demyelination and gliosis throughout the white matter; the cerebellar cortex showed atrophy. The striking, unexpected finding was the presence of numerous Alzheimer's tangles containing paired helical filaments in electronmicroscopic examination, not only in the cerebral cortex but also in the brainstem, basal ganglia, and hypothalamus including the nucleus basalis of Meynert. Other unusual findings were hyperostosis of the skull and the appearance of macrophages containing PAS-positive granules in the reticuloendothelial system in many organs.
我们报告一例具有一些嗜苏丹性特征的婴儿型脑白质营养不良病例。一名发育正常的男婴,直到15个月大时情况良好。随后,他出现肌阵挛发作、智力发育倒退、强直伴去大脑强直姿势以及癫痫发作,且病情逐渐加重。他于7岁10个月时死亡。尸检发现,大脑发育正常,但整个白质存在严重脱髓鞘和胶质增生;小脑皮质出现萎缩。令人惊讶的意外发现是,在电子显微镜检查中,不仅在大脑皮质,而且在脑干、基底神经节和下丘脑(包括Meynert基底核)均发现大量含有双螺旋丝的阿尔茨海默病缠结。其他不寻常的发现包括颅骨骨质增生以及许多器官的网状内皮系统中出现含有PAS阳性颗粒的巨噬细胞。