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Title:
Progressive supranuclear palsy (PSP): a quantitative study of the pathological changes in cortical and subcortical regions of eight cases | Journal of Neural Transmission
Description:
In eight cases of progressive supranuclear palsy (PSP), neurofibrillary tangles (NFT) were numerous in the substantia nigra (SN), red nucleus (RN), locus caeruleus (LC), pontine nuclei (PN), and inferior olivary nucleus (ION) and abnormally enlarged neurons (EN) in the ION, LC and PN. Loss of Purkinje cells was evident in the cerebellum. Tufted astrocytes (TA) were abundant in the striatum, SN and RN and glial inclusions (‘coiled bodies’) (GI) in the midbrain (SN, RN) and pons (LC). Neuritic plaques were frequent in one case. NFT, GI, and TA densities were uncorrelated in most areas. NFT and EN densities were positively correlated in the midbrain and surviving neurons and disease duration in several areas. These results suggest: 1) predominantly subcortical pathology in PSP with widespread NFT while TA and GI have a more localized distribution, 2) little correlation between neuronal and glial pathologies, and 3) shorter duration cases may be more likely to develop cortical pathology.
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google, scholar, article, progressive, supranuclear, palsy, pubmed, cas, neuropathol, brain, neurol, acta, disease, pathology, cortical, lantos, syndrome, degeneration, study, armstrong, tau, clinical, dickson, psp, cairns, tangles, astrocytes, access, neurology, braak, corticobasal, steelerichardsonolszewski, neuropathological, privacy, cookies, content, data, journal, quantitative, pathological, cases, nft, glial, distribution, exp, lees, publish, research, search, neural,
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gadea-domenech jf navarro-humanes dickson ds horoupian ben-shlomo np quinn month download article/chapter duyckaerts jj hauw dyak2szivvwjtw%3d%3d 10 dyak1mvksfsqtg%3d%3d 10 togo dw dickson jellinger pl lantos revesz aj lees steele-richardson-olszewski syndrome tellez-nagel hm wisniewski kilford jl holton jellinger dw anderson article armstrong full article pdf gonzalez dc mash lee jq trojanowski montpetit df clapin progressive supranuclear palsy yamada pl mcgeer cortical-basal ganglionic degeneration basal ganglia access privacy choices/manage cookies clinical research criteria weyer ae lang neural transmission aims cairns rights article journal 1007/s00401-002-0520-1 1 related subjects disease references article log multiple system atrophy lamina-specific pathology distinct clinical phenotypes corticobasal degeneration brain article cite regional cerebral atrophy european economic area scope submit manuscript mossy fiber involvement primitive β-amyloid bergeron ms pollanen reich na muma grafman jh growden jankovic np quinn juncos kb nelson pramstaller sg reich rojo rs pernaute
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headline:Progressive supranuclear palsy (PSP): a quantitative study of the pathological changes in cortical and subcortical regions of eight cases
description:In eight cases of progressive supranuclear palsy (PSP), neurofibrillary tangles (NFT) were numerous in the substantia nigra (SN), red nucleus (RN), locus caeruleus (LC), pontine nuclei (PN), and inferior olivary nucleus (ION) and abnormally enlarged neurons (EN) in the ION, LC and PN. Loss of Purkinje cells was evident in the cerebellum. Tufted astrocytes (TA) were abundant in the striatum, SN and RN and glial inclusions (‘coiled bodies’) (GI) in the midbrain (SN, RN) and pons (LC). Neuritic plaques were frequent in one case. NFT, GI, and TA densities were uncorrelated in most areas. NFT and EN densities were positively correlated in the midbrain and surviving neurons and disease duration in several areas. These results suggest: 1) predominantly subcortical pathology in PSP with widespread NFT while TA and GI have a more localized distribution, 2) little correlation between neuronal and glial pathologies, and 3) shorter duration cases may be more likely to develop cortical pathology.
datePublished:2007-08-07T00:00:00Z
dateModified:2007-08-07T00:00:00Z
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Keywords: Progressive supranuclear palsy (PSP); neurofibrillary tangles (NFT); tufted astrocytes (TA); glial inclusions (GI); neuritic plaques; frontal cortex; basal ganglia
Neurology
Psychiatry
Neurosciences
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headline:Progressive supranuclear palsy (PSP): a quantitative study of the pathological changes in cortical and subcortical regions of eight cases
description:In eight cases of progressive supranuclear palsy (PSP), neurofibrillary tangles (NFT) were numerous in the substantia nigra (SN), red nucleus (RN), locus caeruleus (LC), pontine nuclei (PN), and inferior olivary nucleus (ION) and abnormally enlarged neurons (EN) in the ION, LC and PN. Loss of Purkinje cells was evident in the cerebellum. Tufted astrocytes (TA) were abundant in the striatum, SN and RN and glial inclusions (‘coiled bodies’) (GI) in the midbrain (SN, RN) and pons (LC). Neuritic plaques were frequent in one case. NFT, GI, and TA densities were uncorrelated in most areas. NFT and EN densities were positively correlated in the midbrain and surviving neurons and disease duration in several areas. These results suggest: 1) predominantly subcortical pathology in PSP with widespread NFT while TA and GI have a more localized distribution, 2) little correlation between neuronal and glial pathologies, and 3) shorter duration cases may be more likely to develop cortical pathology.
datePublished:2007-08-07T00:00:00Z
dateModified:2007-08-07T00:00:00Z
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Neurology
Psychiatry
Neurosciences
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