Hippocampal pathology in progressive supranuclear palsy (PSP): a quantitative study of 8 cases

被引:0
作者
Armstrong, R. A. [1 ]
Lantos, P. L. [2 ]
Cairns, N. J. [3 ,4 ,5 ]
机构
[1] Aston Univ, Birmingham BE 7ET, W Midlands, England
[2] Kings Coll London, Inst Psychiat, Dept Neuropathol, London WC2R 2LS, England
[3] Washington Univ, Sch Med, Dept Neurol, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Dept Pathol, St Louis, MO 63110 USA
[5] Washington Univ, Sch Med, Dept Immunol, St Louis, MO 63110 USA
关键词
progressive supranuclear palsy (PSP); neurofibrillary tangle (NFT); glial inclusion (coiled body) (GI); neuritic plaque (NP); hippocampus; MULTIPLE SYSTEM ATROPHY; CORTICOBASAL DEGENERATION; ALZHEIMERS-DISEASE; NEUROFIBRILLARY TANGLES; PARKINSONS-DISEASE; CORTICAL PATHOLOGY; SPATIAL-PATTERNS; PICKS-DISEASE; BRAIN-TISSUE; WHITE-MATTER;
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To quantify the neuronal and glial cell pathology in the hippocampus and the parahippocampal gyrus (PHG) of 8 cases of progressive supranuclear palsy (PSP). Material: tau-immunolabeled sections of the teniporal lobe of 8 diagnosed cases of PSR Method: The densities of lesions were measured in the PHG, CA sectors of the hippocampus and the dentate gyrus (DG) and studied using spatial pattern analysis. Results: Neurofibrillary tangles (NFT) and abnormally enlarged neurons (EN) were most frequent in the PHG and in sector CA1 of the hippocampus, oligodendroglial inclusions ("coiled bodies") (G1) in the PHG, subiculum, sectors CA1 and CA2, and neuritic plaques (NP) in sectors CA2 and CA4. The DG Was the least affected region. Vacuolation and GI were observed in the alveus. No tufted astrocytes(TA)were observed. Pathological changes exhibited clustering, the lesions of the exhibiting a regular distribution of the clusters parallel to the tissue boundary. There was 1 positive correlation between the degree or vacuolation ill the alveus and the densities of NFT in CA1 and G1 in CA1 and CA2. Conclusion: The pathology most significantly affected the Output pathways of the hippocampus, lesions were topographically distributed and hippocampal pathology may be one factor, contributing to cognitive decline in PSP.
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页码:46 / 53
页数:8
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