Morphological overlap between corticobasal degeneration and Pick's disease: A clinicopathological report
Identifieur interne : 003592 ( Istex/Corpus ); précédent : 003591; suivant : 003593Morphological overlap between corticobasal degeneration and Pick's disease: A clinicopathological report
Auteurs : Klaus Jendroska ; Martin N. Rossor ; Christopher J. Mathias ; DanielSource :
- Movement Disorders [ 0885-3185 ] ; 1995-01.
English descriptors
- KwdEn :
Abstract
An 81‐year‐old woman died after a 3‐year history of a progressive nondementing akinetic‐rigid syndrome. Initially, there was a moderate response to levodopa treatment. Subsequently she developed postural tremor, loss of upward gaze, and frequent falls suggestive of Steele‐Richardson‐Olszewski syndrome (SROS). Macroscopical examination showed depigmentation of substantia nigra and locus ceruleus. Histology revealed occasional swollen achromatic neurons predominantly in frontal cortex, small cortical neurofibrillary tangles, brain stem basophil (corticobasal) inclusions, and Pick bodies. The coexistence of these histopathological markers raises questions concerning their specificity and the basis of a morphological distinction between corticobasal degeneration and Pick's disease.
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DOI: 10.1002/mds.870100118
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ISTEX:77D6458F5CE9A1B428768C963B83FF235D3A8C97Le document en format XML
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Initially, there was a moderate response to levodopa treatment. Subsequently she developed postural tremor, loss of upward gaze, and frequent falls suggestive of Steele‐Richardson‐Olszewski syndrome (SROS). Macroscopical examination showed depigmentation of substantia nigra and locus ceruleus. Histology revealed occasional swollen achromatic neurons predominantly in frontal cortex, small cortical neurofibrillary tangles, brain stem basophil (corticobasal) inclusions, and Pick bodies. The coexistence of these histopathological markers raises questions concerning their specificity and the basis of a morphological distinction between corticobasal degeneration and Pick's disease.</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>Klaus Jendroska</name><affiliations><json:string>Parkinson's Disease Society Brain Bank, London</json:string><json:string>Institute of Neurology, London</json:string></affiliations></json:item><json:item><name>Martin N. Rossor</name><affiliations><json:string>Department of Neurology, Universitätsklinikum Rudolf Virchow, Berlin, Germany</json:string><json:string>Department of Neurology, St Mary's Hospital Medical School, London, England</json:string></affiliations></json:item><json:item><name>Christopher J. Mathias</name><affiliations><json:string>Department of Neurology, Universitätsklinikum Rudolf Virchow, Berlin, Germany</json:string><json:string>Department of Neurology, St Mary's Hospital Medical School, London, England</json:string><json:string>Imperial College of Science, Technology, and Medicine, The National Hospital for Neurology and Neurosurgery, London, England</json:string></affiliations></json:item><json:item><name>Dr. Daniel</name><affiliations><json:string>Parkinson's Disease Society Brain Bank, London</json:string><json:string>Department of Neurology, Universitätsklinikum Rudolf Virchow, Berlin, Germany</json:string><json:string>Department of Neuropathology, The National Hospital for Neurology and Neurosurgery, London, England</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>Corticobasal degeneration</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Pick's disease</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Swollen neuron</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Pick body</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Basophil inclusion</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Neurofibrillary tangle</value></json:item></subject><language><json:string>eng</json:string></language><abstract>An 81‐year‐old woman died after a 3‐year history of a progressive nondementing akinetic‐rigid syndrome. 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Initially, there was a moderate response to levodopa treatment. Subsequently she developed postural tremor, loss of upward gaze, and frequent falls suggestive of Steele‐Richardson‐Olszewski syndrome (SROS). Macroscopical examination showed depigmentation of substantia nigra and locus ceruleus. Histology revealed occasional swollen achromatic neurons predominantly in frontal cortex, small cortical neurofibrillary tangles, brain stem basophil (corticobasal) inclusions, and Pick bodies. The coexistence of these histopathological markers raises questions concerning their specificity and the basis of a morphological distinction between corticobasal degeneration and Pick's disease.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><!--Version 0.6 générée le 3-12-2015--><mods version="3.6"><titleInfo lang="en"><title>Morphological overlap between corticobasal degeneration and Pick's disease: A clinicopathological report</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>CORTICOBASAL DEGENERATION AND PICK'S DISEASE</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Morphological overlap between corticobasal degeneration and Pick's disease: A clinicopathological report</title></titleInfo><name type="personal"><namePart type="given">Klaus</namePart><namePart type="family">Jendroska</namePart><affiliation>Parkinson's Disease Society Brain Bank, London</affiliation><affiliation>Institute of Neurology, London</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Martin N.</namePart><namePart type="family">Rossor</namePart><affiliation>Department of Neurology, Universitätsklinikum Rudolf Virchow, Berlin, Germany</affiliation><affiliation>Department of Neurology, St Mary's Hospital Medical School, London, England</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Christopher J.</namePart><namePart type="family">Mathias</namePart><affiliation>Department of Neurology, Universitätsklinikum Rudolf Virchow, Berlin, Germany</affiliation><affiliation>Department of Neurology, St Mary's Hospital Medical School, London, England</affiliation><affiliation>Imperial College of Science, Technology, and Medicine, The National Hospital for Neurology and Neurosurgery, London, England</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="termsOfAddress">Dr.</namePart><namePart type="family">Daniel</namePart><affiliation>Parkinson's Disease Society Brain Bank, London</affiliation><affiliation>Department of Neurology, Universitätsklinikum Rudolf Virchow, Berlin, Germany</affiliation><affiliation>Department of Neuropathology, The National Hospital for Neurology and Neurosurgery, London, England</affiliation><description>Correspondence: Parkinson's Disease Society Brain Bank, 1 Wakefield Street, London WC1N 1PJ, England</description><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre authority="originalCategForm">article</genre><originInfo><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><place><placeTerm type="text">Hoboken</placeTerm></place><dateIssued encoding="w3cdtf">1995-01</dateIssued><dateValid encoding="w3cdtf">1994-07-26</dateValid><copyrightDate encoding="w3cdtf">1995</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType><extent unit="figures">4</extent><extent unit="references">14</extent></physicalDescription><abstract lang="en">An 81‐year‐old woman died after a 3‐year history of a progressive nondementing akinetic‐rigid syndrome. Initially, there was a moderate response to levodopa treatment. Subsequently she developed postural tremor, loss of upward gaze, and frequent falls suggestive of Steele‐Richardson‐Olszewski syndrome (SROS). Macroscopical examination showed depigmentation of substantia nigra and locus ceruleus. Histology revealed occasional swollen achromatic neurons predominantly in frontal cortex, small cortical neurofibrillary tangles, brain stem basophil (corticobasal) inclusions, and Pick bodies. The coexistence of these histopathological markers raises questions concerning their specificity and the basis of a morphological distinction between corticobasal degeneration and Pick's disease.</abstract><subject lang="en"><genre>Keywords</genre><topic>Corticobasal degeneration</topic><topic>Pick's disease</topic><topic>Swollen neuron</topic><topic>Pick body</topic><topic>Basophil inclusion</topic><topic>Neurofibrillary tangle</topic></subject><relatedItem type="host"><titleInfo><title>Movement Disorders</title><subTitle>Official Journal of the Movement Disorder Society</subTitle></titleInfo><titleInfo type="abbreviated"><title>Mov. Disord.</title></titleInfo><subject><genre>article category</genre><topic>Brief Report</topic></subject><identifier type="ISSN">0885-3185</identifier><identifier type="eISSN">1531-8257</identifier><identifier type="DOI">10.1002/(ISSN)1531-8257</identifier><identifier type="PublisherID">MDS</identifier><part><date>1995</date><detail type="volume"><caption>vol.</caption><number>10</number></detail><detail type="issue"><caption>no.</caption><number>1</number></detail><extent unit="pages"><start>111</start><end>114</end><total>4</total></extent></part></relatedItem><identifier type="istex">77D6458F5CE9A1B428768C963B83FF235D3A8C97</identifier><identifier type="DOI">10.1002/mds.870100118</identifier><identifier type="ArticleID">MDS870100118</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 1995 Movement Disorder Society</accessCondition><recordInfo><recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin><recordContentSource>WILEY</recordContentSource></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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|texte= Morphological overlap between corticobasal degeneration and Pick's disease: A clinicopathological report
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