de León G A, Grover W D, Huff D S, Morinigo-Mestre G, Punnett H H, Kistenmacher M L
Ann Neurol. 1977 Dec;2(6):473-84. doi: 10.1002/ana.410020606.
In addition to a distinct malformation (pachymicrogyria, heterotaxic lamination of the cerebellar cortex, olivary dysplasia), unusual degenerative changes were found in the nervous system of 2 unrelated babies with the Zellweger syndrome. Cerebral clefts were present in 1 case. In both infants there was neuron loss and accumulation of glial nodules and globoid cells in the gray matter as well as degeneration of the white matter. There was fatty change in astrocytes and diffuse gliosis. Neurons in the column of Clarke and the lateral cuneate nucleus showed peculiar fibrillary changes. Cytoplasmic inclusion bodies were seen in the spinal ganglia. Swelling of cortical astrocytes was remarkable in the older infant. The combination of a rare malformation with the cell changes described here gives the syndrome a unique neuropathological profile.
除了明显的畸形(厚层微脑回、小脑皮质异位分层、橄榄体发育异常)外,在2例无关的患有泽尔韦格综合征的婴儿的神经系统中还发现了不寻常的退行性变化。1例存在脑裂。两名婴儿均有神经元丢失,灰质中胶质结节和球状细胞积聚,以及白质变性。星形胶质细胞出现脂肪变性和弥漫性胶质增生。克拉克柱和外侧楔状核中的神经元显示出特殊的纤维变化。脊髓神经节中可见细胞质包涵体。在较大的婴儿中,皮质星形胶质细胞肿胀明显。这种罕见畸形与本文所述细胞变化的结合赋予了该综合征独特的神经病理学特征。