Atypical Parkinsonism combining α-synuclein inclusions and polyglucosan body disease
Identifieur interne : 005404 ( Main/Merge ); précédent : 005403; suivant : 005405Atypical Parkinsonism combining α-synuclein inclusions and polyglucosan body disease
Auteurs : Elsa Krim [France] ; Anne Vital [France] ; Frederic Macia [France] ; Farid Yekhlef [France] ; Francois Tison [France]Source :
- Movement disorders [ 0885-3185 ] ; 2005.
Descripteurs français
- Pascal (Inist)
English descriptors
Abstract
Adult polyglucosan body disease (APGBD) is a rare disorder affecting the central and peripheral nervous systems and in which parkinsonism is unusual. A 71-year-old man presented levodopa-unresponsive parkinsonism with urinary incontinence and recurrent syncopes of 6 years standing masquerading as atypical parkinsonism of the multiple system atrophy (MSA-P) type. Brain histopathology demonstrated massive accumulation of polyglucosan bodies particularly in the putamen. In addition, there were dense α-synuclein-positive cytoplasmic oligodendroglial inclusions in the pons and in the middle cerebellar peduncle. These inclusions may be either due to the chance association of MSA-P with APGBD, or pathologically related to APGBD.
Links toward previous steps (curation, corpus...)
- to stream PascalFrancis, to step Corpus: 001F60
- to stream PascalFrancis, to step Curation: 000D61
- to stream PascalFrancis, to step Checkpoint: 001F26
Links to Exploration step
Pascal:05-0151000Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Atypical Parkinsonism combining α-synuclein inclusions and polyglucosan body disease</title>
<author><name sortKey="Krim, Elsa" sort="Krim, Elsa" uniqKey="Krim E" first="Elsa" last="Krim">Elsa Krim</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Service de Neurologie, Centre Hospitalier Universitaire de Bordeaux</s1>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>France</country>
<wicri:noRegion>Centre Hospitalier Universitaire de Bordeaux</wicri:noRegion>
<wicri:noRegion>Service de Neurologie, Centre Hospitalier Universitaire de Bordeaux</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Vital, Anne" sort="Vital, Anne" uniqKey="Vital A" first="Anne" last="Vital">Anne Vital</name>
<affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Service d'Anatomopathologie, Centre Hospitalier Universitaire de Bordeaux</s1>
<s3>FRA</s3>
<sZ>2 aut.</sZ>
</inist:fA14>
<country>France</country>
<wicri:noRegion>Centre Hospitalier Universitaire de Bordeaux</wicri:noRegion>
<wicri:noRegion>Service d'Anatomopathologie, Centre Hospitalier Universitaire de Bordeaux</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Macia, Frederic" sort="Macia, Frederic" uniqKey="Macia F" first="Frederic" last="Macia">Frederic Macia</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Service de Neurologie, Centre Hospitalier Universitaire de Bordeaux</s1>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>France</country>
<wicri:noRegion>Centre Hospitalier Universitaire de Bordeaux</wicri:noRegion>
<wicri:noRegion>Service de Neurologie, Centre Hospitalier Universitaire de Bordeaux</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Yekhlef, Farid" sort="Yekhlef, Farid" uniqKey="Yekhlef F" first="Farid" last="Yekhlef">Farid Yekhlef</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Service de Neurologie, Centre Hospitalier Universitaire de Bordeaux</s1>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>France</country>
<wicri:noRegion>Centre Hospitalier Universitaire de Bordeaux</wicri:noRegion>
<wicri:noRegion>Service de Neurologie, Centre Hospitalier Universitaire de Bordeaux</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Tison, Francois" sort="Tison, Francois" uniqKey="Tison F" first="Francois" last="Tison">Francois Tison</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Service de Neurologie, Centre Hospitalier Universitaire de Bordeaux</s1>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>France</country>
<wicri:noRegion>Centre Hospitalier Universitaire de Bordeaux</wicri:noRegion>
<wicri:noRegion>Service de Neurologie, Centre Hospitalier Universitaire de Bordeaux</wicri:noRegion>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">INIST</idno>
<idno type="inist">05-0151000</idno>
<date when="2005">2005</date>
<idno type="stanalyst">PASCAL 05-0151000 INIST</idno>
<idno type="RBID">Pascal:05-0151000</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">001F60</idno>
<idno type="wicri:Area/PascalFrancis/Curation">000D61</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">001F26</idno>
<idno type="wicri:doubleKey">0885-3185:2005:Krim E:atypical:parkinsonism:combining</idno>
<idno type="wicri:Area/Main/Merge">005404</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Atypical Parkinsonism combining α-synuclein inclusions and polyglucosan body disease</title>
<author><name sortKey="Krim, Elsa" sort="Krim, Elsa" uniqKey="Krim E" first="Elsa" last="Krim">Elsa Krim</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Service de Neurologie, Centre Hospitalier Universitaire de Bordeaux</s1>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>France</country>
<wicri:noRegion>Centre Hospitalier Universitaire de Bordeaux</wicri:noRegion>
<wicri:noRegion>Service de Neurologie, Centre Hospitalier Universitaire de Bordeaux</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Vital, Anne" sort="Vital, Anne" uniqKey="Vital A" first="Anne" last="Vital">Anne Vital</name>
<affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Service d'Anatomopathologie, Centre Hospitalier Universitaire de Bordeaux</s1>
<s3>FRA</s3>
<sZ>2 aut.</sZ>
</inist:fA14>
<country>France</country>
<wicri:noRegion>Centre Hospitalier Universitaire de Bordeaux</wicri:noRegion>
<wicri:noRegion>Service d'Anatomopathologie, Centre Hospitalier Universitaire de Bordeaux</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Macia, Frederic" sort="Macia, Frederic" uniqKey="Macia F" first="Frederic" last="Macia">Frederic Macia</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Service de Neurologie, Centre Hospitalier Universitaire de Bordeaux</s1>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>France</country>
<wicri:noRegion>Centre Hospitalier Universitaire de Bordeaux</wicri:noRegion>
<wicri:noRegion>Service de Neurologie, Centre Hospitalier Universitaire de Bordeaux</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Yekhlef, Farid" sort="Yekhlef, Farid" uniqKey="Yekhlef F" first="Farid" last="Yekhlef">Farid Yekhlef</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Service de Neurologie, Centre Hospitalier Universitaire de Bordeaux</s1>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>France</country>
<wicri:noRegion>Centre Hospitalier Universitaire de Bordeaux</wicri:noRegion>
<wicri:noRegion>Service de Neurologie, Centre Hospitalier Universitaire de Bordeaux</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Tison, Francois" sort="Tison, Francois" uniqKey="Tison F" first="Francois" last="Tison">Francois Tison</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Service de Neurologie, Centre Hospitalier Universitaire de Bordeaux</s1>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>France</country>
<wicri:noRegion>Centre Hospitalier Universitaire de Bordeaux</wicri:noRegion>
<wicri:noRegion>Service de Neurologie, Centre Hospitalier Universitaire de Bordeaux</wicri:noRegion>
</affiliation>
</author>
</analytic>
<series><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
<imprint><date when="2005">2005</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Inclusion body</term>
<term>Nervous system diseases</term>
<term>Parkinsonism</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Système nerveux pathologie</term>
<term>Corps inclusion</term>
<term>Parkinsonisme</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Adult polyglucosan body disease (APGBD) is a rare disorder affecting the central and peripheral nervous systems and in which parkinsonism is unusual. A 71-year-old man presented levodopa-unresponsive parkinsonism with urinary incontinence and recurrent syncopes of 6 years standing masquerading as atypical parkinsonism of the multiple system atrophy (MSA-P) type. Brain histopathology demonstrated massive accumulation of polyglucosan bodies particularly in the putamen. In addition, there were dense α-synuclein-positive cytoplasmic oligodendroglial inclusions in the pons and in the middle cerebellar peduncle. These inclusions may be either due to the chance association of MSA-P with APGBD, or pathologically related to APGBD.</div>
</front>
</TEI>
<affiliations><list><country><li>France</li>
</country>
</list>
<tree><country name="France"><noRegion><name sortKey="Krim, Elsa" sort="Krim, Elsa" uniqKey="Krim E" first="Elsa" last="Krim">Elsa Krim</name>
</noRegion>
<name sortKey="Macia, Frederic" sort="Macia, Frederic" uniqKey="Macia F" first="Frederic" last="Macia">Frederic Macia</name>
<name sortKey="Tison, Francois" sort="Tison, Francois" uniqKey="Tison F" first="Francois" last="Tison">Francois Tison</name>
<name sortKey="Vital, Anne" sort="Vital, Anne" uniqKey="Vital A" first="Anne" last="Vital">Anne Vital</name>
<name sortKey="Yekhlef, Farid" sort="Yekhlef, Farid" uniqKey="Yekhlef F" first="Farid" last="Yekhlef">Farid Yekhlef</name>
</country>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Main/Merge
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 005404 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Merge/biblio.hfd -nk 005404 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Santé |area= MovDisordV3 |flux= Main |étape= Merge |type= RBID |clé= Pascal:05-0151000 |texte= Atypical Parkinsonism combining α-synuclein inclusions and polyglucosan body disease }}
![]() | This area was generated with Dilib version V0.6.23. | ![]() |