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Spatial patterns of the pathological changes in neuronal intermediate filament inclusion disease (NIFID): an α-internexin immunohistochemical study

机译:神经元中间丝包裹体疾病(NIFID)的病理变化的空间模式:α-internexin免疫组化研究

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Neuronal intermediate filament inclusion disease (NIFID) is characterized by α-internexin positive neuronal cytoplasmic inclusions (NCI), swollen achromatic neurons (SN), neuronal loss, and gliosis. This study tested: 1) whether the spatial patterns of the lesions was topographically organized in areas of the frontal and temporal lobe and 2) whether a spatial relationship exists between the NCI and SN. The NCI were distributed in regular clusters and in a quarter of these areas, the clusters were 400–800 μm in diameter approximating to the size of the cells of origin of the cortico-cortical pathways. Variations in the density of the NCI were positively correlated with the SN. Hence, cortical degeneration in NIFID appears to be topographically organized and may affect the cortico-cortical projections, the clusters of NCI and SN developing within the same vertical columns of cells.
机译:神经元中间丝包裹体疾病(NIFID)的特征在于α-internexin阳性神经元胞浆包裹体(NCI),消色差性神经元(SN)肿胀,神经元丢失和神经胶质增生。这项研究测试:1)病变的空间模式是否在额叶和颞叶区域进行了地形组织,以及2)NCI和SN之间是否存在空间关系。 NCI分布在规则的簇中,并且在这些区域的四分之一中,簇的直径为400-800μm,近似于皮质-皮质途径起源细胞的大小。 NCI密度的变化与SN正相关。因此,NIFID中的皮质变性似乎是按地形组织的,并且可能影响皮质皮质投影,NCI和SN的簇在同一垂直列细胞内发育。

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