Armstrong R A, Cairns N J
Vision Sciences, Aston University, Birmingham, UK.
J Neural Transm (Vienna). 2007;114(4):451-6. doi: 10.1007/s00702-006-0595-2. Epub 2006 Nov 17.
Neuronal intermediate filament inclusion disease (NIFID) is characterized by alpha-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 microm 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.
神经元中间丝包涵体病(NIFID)的特征是α-中间丝蛋白阳性的神经元胞质包涵体(NCI)、肿胀的无色神经元(SN)、神经元丢失和胶质细胞增生。本研究检测了:1)额叶和颞叶区域病变的空间模式是否按地形组织;2)NCI和SN之间是否存在空间关系。NCI呈规则簇状分布,在这些区域的四分之一中,簇的直径为400 - 800微米,近似于皮质 - 皮质通路起源细胞的大小。NCI密度的变化与SN呈正相关。因此,NIFID中的皮质变性似乎是按地形组织的,可能会影响皮质 - 皮质投射,NCI和SN簇在同一垂直细胞柱内发展。