ParkinsonFranceV1, Ncbi, Merge, bibRecord, 000E79

Camptocormia as a clinical manifestation of polymyositis/systemic sclerosis overlap myositis associated with anti-Ku.

Identifieur interne : 000E79 ( Ncbi/Merge ); précédent : 000E78; suivant : 000E80

Camptocormia as a clinical manifestation of polymyositis/systemic sclerosis overlap myositis associated with anti-Ku.

Auteurs : Thierry Zenone [France] ; Nathalie Streichenberger ; Marie Puget

Source :

Rheumatology international [ 1437-160X ] ; 2013.

RBID : pubmed:22453528

English descriptors

KwdEn :
- Aged, Antigens, Nuclear (immunology), Autoantibodies (blood), DNA-Binding Proteins (immunology), Humans, Ku Autoantigen, Male, Muscular Atrophy, Spinal (etiology), Polymyositis (complications), Polymyositis (pathology), Scleroderma, Systemic (complications), Scleroderma, Systemic (pathology), Spinal Curvatures (etiology).
MESH :
- chemical , blood : Autoantibodies.
- chemical , immunology : Antigens, Nuclear, DNA-Binding Proteins.
- complications : Polymyositis, Scleroderma, Systemic.
- etiology : Muscular Atrophy, Spinal, Spinal Curvatures.
- pathology : Polymyositis, Scleroderma, Systemic.
- Aged, Humans, Ku Autoantigen, Male.

Abstract

Camptocormia, an abnormal truncal flexion posture that occurs while walking or standing, is usually caused by various hypokinetic movement disorders, mainly Parkinson disease. We describe the case of a man with subacute onset of camptocormia. Quadriceps muscle biopsy showed significant rhabdomyolysis, few isolated inflammatory cells and mild expression of type I MHC in few fibers, a pattern usually found in immune-mediated necrotizing myopathies. Myositis was associated with Raynaud's phenomenon, mild sclerodactyly, and anti-Ku antibodies leading to the diagnosis of polymyositis/systemic sclerosis overlap myositis. The posture showed modest improvement in response to treatment.

DOI: 10.1007/s00296-012-2412-6
PubMed: 22453528

Links toward previous steps (curation, corpus...)

to stream PubMed, to step Corpus: 000703
to stream PubMed, to step Curation: 000672
to stream PubMed, to step Checkpoint: 000672

Links to Exploration step

pubmed:22453528

Le document en format XML

<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Camptocormia as a clinical manifestation of polymyositis/systemic sclerosis overlap myositis associated with anti-Ku.</title>
<author><name sortKey="Zenone, Thierry" sort="Zenone, Thierry" uniqKey="Zenone T" first="Thierry" last="Zenone">Thierry Zenone</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Internal Medicine, Centre Hospitalier, 179 boulevard Marechal Juin, 26953, Valence Cedex 9, France. tzenone@ch-valence.fr</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>Department of Internal Medicine, Centre Hospitalier, 179 boulevard Marechal Juin, 26953, Valence Cedex 9</wicri:regionArea>
<placeName><region type="region" nuts="2">Auvergne-Rhône-Alpes</region>
<region type="old region" nuts="2">Rhône-Alpes</region>
<settlement type="city">Valence</settlement>
</placeName>
</affiliation>
</author>
<author><name sortKey="Streichenberger, Nathalie" sort="Streichenberger, Nathalie" uniqKey="Streichenberger N" first="Nathalie" last="Streichenberger">Nathalie Streichenberger</name>
</author>
<author><name sortKey="Puget, Marie" sort="Puget, Marie" uniqKey="Puget M" first="Marie" last="Puget">Marie Puget</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="2013">2013</date>
<idno type="RBID">pubmed:22453528</idno>
<idno type="pmid">22453528</idno>
<idno type="doi">10.1007/s00296-012-2412-6</idno>
<idno type="wicri:Area/PubMed/Corpus">000703</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">000703</idno>
<idno type="wicri:Area/PubMed/Curation">000672</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">000672</idno>
<idno type="wicri:Area/PubMed/Checkpoint">000672</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">000672</idno>
<idno type="wicri:Area/Ncbi/Merge">000E79</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">Camptocormia as a clinical manifestation of polymyositis/systemic sclerosis overlap myositis associated with anti-Ku.</title>
<author><name sortKey="Zenone, Thierry" sort="Zenone, Thierry" uniqKey="Zenone T" first="Thierry" last="Zenone">Thierry Zenone</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Internal Medicine, Centre Hospitalier, 179 boulevard Marechal Juin, 26953, Valence Cedex 9, France. tzenone@ch-valence.fr</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>Department of Internal Medicine, Centre Hospitalier, 179 boulevard Marechal Juin, 26953, Valence Cedex 9</wicri:regionArea>
<placeName><region type="region" nuts="2">Auvergne-Rhône-Alpes</region>
<region type="old region" nuts="2">Rhône-Alpes</region>
<settlement type="city">Valence</settlement>
</placeName>
</affiliation>
</author>
<author><name sortKey="Streichenberger, Nathalie" sort="Streichenberger, Nathalie" uniqKey="Streichenberger N" first="Nathalie" last="Streichenberger">Nathalie Streichenberger</name>
</author>
<author><name sortKey="Puget, Marie" sort="Puget, Marie" uniqKey="Puget M" first="Marie" last="Puget">Marie Puget</name>
</author>
</analytic>
<series><title level="j">Rheumatology international</title>
<idno type="eISSN">1437-160X</idno>
<imprint><date when="2013" type="published">2013</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term>
<term>Antigens, Nuclear (immunology)</term>
<term>Autoantibodies (blood)</term>
<term>DNA-Binding Proteins (immunology)</term>
<term>Humans</term>
<term>Ku Autoantigen</term>
<term>Male</term>
<term>Muscular Atrophy, Spinal (etiology)</term>
<term>Polymyositis (complications)</term>
<term>Polymyositis (pathology)</term>
<term>Scleroderma, Systemic (complications)</term>
<term>Scleroderma, Systemic (pathology)</term>
<term>Spinal Curvatures (etiology)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="blood" xml:lang="en"><term>Autoantibodies</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="immunology" xml:lang="en"><term>Antigens, Nuclear</term>
<term>DNA-Binding Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Polymyositis</term>
<term>Scleroderma, Systemic</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Muscular Atrophy, Spinal</term>
<term>Spinal Curvatures</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Polymyositis</term>
<term>Scleroderma, Systemic</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Aged</term>
<term>Humans</term>
<term>Ku Autoantigen</term>
<term>Male</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Camptocormia, an abnormal truncal flexion posture that occurs while walking or standing, is usually caused by various hypokinetic movement disorders, mainly Parkinson disease. We describe the case of a man with subacute onset of camptocormia. Quadriceps muscle biopsy showed significant rhabdomyolysis, few isolated inflammatory cells and mild expression of type I MHC in few fibers, a pattern usually found in immune-mediated necrotizing myopathies. Myositis was associated with Raynaud's phenomenon, mild sclerodactyly, and anti-Ku antibodies leading to the diagnosis of polymyositis/systemic sclerosis overlap myositis. The posture showed modest improvement in response to treatment.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">22453528</PMID>
<DateCreated><Year>2013</Year>
<Month>08</Month>
<Day>26</Day>
</DateCreated>
<DateCompleted><Year>2014</Year>
<Month>06</Month>
<Day>13</Day>
</DateCompleted>
<DateRevised><Year>2016</Year>
<Month>11</Month>
<Day>25</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1437-160X</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>33</Volume>
<Issue>9</Issue>
<PubDate><Year>2013</Year>
<Month>Sep</Month>
</PubDate>
</JournalIssue>
<Title>Rheumatology international</Title>
<ISOAbbreviation>Rheumatol. Int.</ISOAbbreviation>
</Journal>
<ArticleTitle>Camptocormia as a clinical manifestation of polymyositis/systemic sclerosis overlap myositis associated with anti-Ku.</ArticleTitle>
<Pagination><MedlinePgn>2411-5</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1007/s00296-012-2412-6</ELocationID>
<Abstract><AbstractText>Camptocormia, an abnormal truncal flexion posture that occurs while walking or standing, is usually caused by various hypokinetic movement disorders, mainly Parkinson disease. We describe the case of a man with subacute onset of camptocormia. Quadriceps muscle biopsy showed significant rhabdomyolysis, few isolated inflammatory cells and mild expression of type I MHC in few fibers, a pattern usually found in immune-mediated necrotizing myopathies. Myositis was associated with Raynaud's phenomenon, mild sclerodactyly, and anti-Ku antibodies leading to the diagnosis of polymyositis/systemic sclerosis overlap myositis. The posture showed modest improvement in response to treatment.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Zenone</LastName>
<ForeName>Thierry</ForeName>
<Initials>T</Initials>
<AffiliationInfo><Affiliation>Department of Internal Medicine, Centre Hospitalier, 179 boulevard Marechal Juin, 26953, Valence Cedex 9, France. tzenone@ch-valence.fr</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Streichenberger</LastName>
<ForeName>Nathalie</ForeName>
<Initials>N</Initials>
</Author>
<Author ValidYN="Y"><LastName>Puget</LastName>
<ForeName>Marie</ForeName>
<Initials>M</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType>
<PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic"><Year>2012</Year>
<Month>03</Month>
<Day>28</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo><Country>Germany</Country>
<MedlineTA>Rheumatol Int</MedlineTA>
<NlmUniqueID>8206885</NlmUniqueID>
<ISSNLinking>0172-8172</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D034961">Antigens, Nuclear</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D001323">Autoantibodies</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D004268">DNA-Binding Proteins</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>EC 3.6.4.12</RegistryNumber>
<NameOfSubstance UI="C000606509">Xrcc6 protein, human</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>EC 4.2.99.-</RegistryNumber>
<NameOfSubstance UI="D000072200">Ku Autoantigen</NameOfSubstance>
</Chemical>
</ChemicalList>
<SupplMeshList><SupplMeshName Type="Disease" UI="C537968">Camptocormia</SupplMeshName>
</SupplMeshList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D034961" MajorTopicYN="N">Antigens, Nuclear</DescriptorName>
<QualifierName UI="Q000276" MajorTopicYN="Y">immunology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D001323" MajorTopicYN="N">Autoantibodies</DescriptorName>
<QualifierName UI="Q000097" MajorTopicYN="Y">blood</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D004268" MajorTopicYN="N">DNA-Binding Proteins</DescriptorName>
<QualifierName UI="Q000276" MajorTopicYN="Y">immunology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D000072200" MajorTopicYN="N">Ku Autoantigen</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D009134" MajorTopicYN="N">Muscular Atrophy, Spinal</DescriptorName>
<QualifierName UI="Q000209" MajorTopicYN="Y">etiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D017285" MajorTopicYN="N">Polymyositis</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D012595" MajorTopicYN="N">Scleroderma, Systemic</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D013121" MajorTopicYN="N">Spinal Curvatures</DescriptorName>
<QualifierName UI="Q000209" MajorTopicYN="Y">etiology</QualifierName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="received"><Year>2011</Year>
<Month>11</Month>
<Day>28</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted"><Year>2012</Year>
<Month>03</Month>
<Day>11</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez"><Year>2012</Year>
<Month>3</Month>
<Day>29</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed"><Year>2012</Year>
<Month>3</Month>
<Day>29</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>2014</Year>
<Month>6</Month>
<Day>15</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">22453528</ArticleId>
<ArticleId IdType="doi">10.1007/s00296-012-2412-6</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations><list><country><li>France</li>
</country>
<region><li>Auvergne-Rhône-Alpes</li>
<li>Rhône-Alpes</li>
</region>
<settlement><li>Valence</li>
</settlement>
</list>
<tree><noCountry><name sortKey="Puget, Marie" sort="Puget, Marie" uniqKey="Puget M" first="Marie" last="Puget">Marie Puget</name>
<name sortKey="Streichenberger, Nathalie" sort="Streichenberger, Nathalie" uniqKey="Streichenberger N" first="Nathalie" last="Streichenberger">Nathalie Streichenberger</name>
</noCountry>
<country name="France"><region name="Auvergne-Rhône-Alpes"><name sortKey="Zenone, Thierry" sort="Zenone, Thierry" uniqKey="Zenone T" first="Thierry" last="Zenone">Thierry Zenone</name>
</region>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/ParkinsonFranceV1/Data/Ncbi/Merge

HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000E79 | SxmlIndent | more

HfdSelect -h $EXPLOR_AREA/Data/Ncbi/Merge/biblio.hfd -nk 000E79 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Sante
   |area=    ParkinsonFranceV1
   |flux=    Ncbi
   |étape=   Merge
   |type=    RBID
   |clé=     pubmed:22453528
   |texte=   Camptocormia as a clinical manifestation of polymyositis/systemic sclerosis overlap myositis associated with anti-Ku.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Ncbi/Merge/RBID.i   -Sk "pubmed:22453528" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Ncbi/Merge/biblio.hfd   \
       | NlmPubMed2Wicri -a ParkinsonFranceV1

This area was generated with Dilib version V0.6.29.
Data generation: Wed May 17 19:46:39 2017. Site generation: Mon Mar 4 15:48:15 2024

	La maladie de Parkinson en France (serveur d'exploration)
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.

La maladie de Parkinson en France (serveur d'exploration)

Camptocormia as a clinical manifestation of polymyositis/systemic sclerosis overlap myositis associated with anti-Ku.

Camptocormia as a clinical manifestation of polymyositis/systemic sclerosis overlap myositis associated with anti-Ku.

Source :

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki