Kawasaki disease complicated by mild encephalopathy with a reversible splenial lesion (MERS).
Identifieur interne : 000904 ( Ncbi/Merge ); précédent : 000903; suivant : 000905Kawasaki disease complicated by mild encephalopathy with a reversible splenial lesion (MERS).
Auteurs : Jun-Ichi Takanashi [Japon] ; Kentaro Shirai ; Yuji Sugawara ; Yoko Okamoto ; Toshimasa Obonai ; Hitoshi TeradaSource :
- Journal of the neurological sciences [ 1878-5883 ] ; 2012.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Corps calleux.
- diagnostic : Encéphalite, Maladie de Kawasaki.
- Encéphalite, Enfant, Enfant d'âge préscolaire, Femelle, Humains, Maladie de Kawasaki, Mâle.
English descriptors
- KwdEn :
- MESH :
- complications : Encephalitis, Mucocutaneous Lymph Node Syndrome.
- diagnosis : Encephalitis, Mucocutaneous Lymph Node Syndrome.
- pathology : Corpus Callosum.
- Child, Child, Preschool, Female, Humans, Male.
Abstract
We reported four patients (2 to 10 years) with Kawasaki disease complicated by clinically mild encephalitis/encephalopathy with a reversible splenial lesion (MERS). All were treated with γ-globulin (2 to 6 g/kg) after the diagnosis of Kawasaki disease, the fever being alleviated between day 6 and 25. One of two patients exhibiting a poor response to γ-globulin had a cardiac aneurysm as a sequela. Their neurological manifestations (delirious behavior and drowsiness), laboratorial hyponatremia, and radiological abnormalities completely disappeared. It is important for pediatricians to acknowledge that MERS can be observed in patients with Kawasaki disease, especially in older children, and that they might be at high risk for cardiac abnormalities.
DOI: 10.1016/j.jns.2011.11.022
PubMed: 22129937
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 001E32
- to stream PubMed, to step Curation: 001E32
- to stream PubMed, to step Checkpoint: 001C66
Links to Exploration step
pubmed:22129937Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Kawasaki disease complicated by mild encephalopathy with a reversible splenial lesion (MERS).</title>
<author><name sortKey="Takanashi, Jun Ichi" sort="Takanashi, Jun Ichi" uniqKey="Takanashi J" first="Jun-Ichi" last="Takanashi">Jun-Ichi Takanashi</name>
<affiliation wicri:level="1"><nlm:affiliation>Department of Pediatrics, Kameda Medical Center, Kamogawa, Japan. jtaka@kameda.jp</nlm:affiliation>
<country xml:lang="fr">Japon</country>
<wicri:regionArea>Department of Pediatrics, Kameda Medical Center, Kamogawa</wicri:regionArea>
<wicri:noRegion>Kamogawa</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Shirai, Kentaro" sort="Shirai, Kentaro" uniqKey="Shirai K" first="Kentaro" last="Shirai">Kentaro Shirai</name>
</author>
<author><name sortKey="Sugawara, Yuji" sort="Sugawara, Yuji" uniqKey="Sugawara Y" first="Yuji" last="Sugawara">Yuji Sugawara</name>
</author>
<author><name sortKey="Okamoto, Yoko" sort="Okamoto, Yoko" uniqKey="Okamoto Y" first="Yoko" last="Okamoto">Yoko Okamoto</name>
</author>
<author><name sortKey="Obonai, Toshimasa" sort="Obonai, Toshimasa" uniqKey="Obonai T" first="Toshimasa" last="Obonai">Toshimasa Obonai</name>
</author>
<author><name sortKey="Terada, Hitoshi" sort="Terada, Hitoshi" uniqKey="Terada H" first="Hitoshi" last="Terada">Hitoshi Terada</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="2012">2012</date>
<idno type="RBID">pubmed:22129937</idno>
<idno type="pmid">22129937</idno>
<idno type="doi">10.1016/j.jns.2011.11.022</idno>
<idno type="wicri:Area/PubMed/Corpus">001E32</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">001E32</idno>
<idno type="wicri:Area/PubMed/Curation">001E32</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">001E32</idno>
<idno type="wicri:Area/PubMed/Checkpoint">001C66</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">001C66</idno>
<idno type="wicri:Area/Ncbi/Merge">000904</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">Kawasaki disease complicated by mild encephalopathy with a reversible splenial lesion (MERS).</title>
<author><name sortKey="Takanashi, Jun Ichi" sort="Takanashi, Jun Ichi" uniqKey="Takanashi J" first="Jun-Ichi" last="Takanashi">Jun-Ichi Takanashi</name>
<affiliation wicri:level="1"><nlm:affiliation>Department of Pediatrics, Kameda Medical Center, Kamogawa, Japan. jtaka@kameda.jp</nlm:affiliation>
<country xml:lang="fr">Japon</country>
<wicri:regionArea>Department of Pediatrics, Kameda Medical Center, Kamogawa</wicri:regionArea>
<wicri:noRegion>Kamogawa</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Shirai, Kentaro" sort="Shirai, Kentaro" uniqKey="Shirai K" first="Kentaro" last="Shirai">Kentaro Shirai</name>
</author>
<author><name sortKey="Sugawara, Yuji" sort="Sugawara, Yuji" uniqKey="Sugawara Y" first="Yuji" last="Sugawara">Yuji Sugawara</name>
</author>
<author><name sortKey="Okamoto, Yoko" sort="Okamoto, Yoko" uniqKey="Okamoto Y" first="Yoko" last="Okamoto">Yoko Okamoto</name>
</author>
<author><name sortKey="Obonai, Toshimasa" sort="Obonai, Toshimasa" uniqKey="Obonai T" first="Toshimasa" last="Obonai">Toshimasa Obonai</name>
</author>
<author><name sortKey="Terada, Hitoshi" sort="Terada, Hitoshi" uniqKey="Terada H" first="Hitoshi" last="Terada">Hitoshi Terada</name>
</author>
</analytic>
<series><title level="j">Journal of the neurological sciences</title>
<idno type="eISSN">1878-5883</idno>
<imprint><date when="2012" type="published">2012</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Child</term>
<term>Child, Preschool</term>
<term>Corpus Callosum (pathology)</term>
<term>Encephalitis (complications)</term>
<term>Encephalitis (diagnosis)</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Mucocutaneous Lymph Node Syndrome (complications)</term>
<term>Mucocutaneous Lymph Node Syndrome (diagnosis)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Corps calleux (anatomopathologie)</term>
<term>Encéphalite ()</term>
<term>Encéphalite (diagnostic)</term>
<term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
<term>Humains</term>
<term>Maladie de Kawasaki ()</term>
<term>Maladie de Kawasaki (diagnostic)</term>
<term>Mâle</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Corps calleux</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Encephalitis</term>
<term>Mucocutaneous Lymph Node Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Encephalitis</term>
<term>Mucocutaneous Lymph Node Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Encéphalite</term>
<term>Maladie de Kawasaki</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Corpus Callosum</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Child</term>
<term>Child, Preschool</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Encéphalite</term>
<term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
<term>Humains</term>
<term>Maladie de Kawasaki</term>
<term>Mâle</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">We reported four patients (2 to 10 years) with Kawasaki disease complicated by clinically mild encephalitis/encephalopathy with a reversible splenial lesion (MERS). All were treated with γ-globulin (2 to 6 g/kg) after the diagnosis of Kawasaki disease, the fever being alleviated between day 6 and 25. One of two patients exhibiting a poor response to γ-globulin had a cardiac aneurysm as a sequela. Their neurological manifestations (delirious behavior and drowsiness), laboratorial hyponatremia, and radiological abnormalities completely disappeared. It is important for pediatricians to acknowledge that MERS can be observed in patients with Kawasaki disease, especially in older children, and that they might be at high risk for cardiac abnormalities.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">22129937</PMID>
<DateCompleted><Year>2012</Year>
<Month>11</Month>
<Day>20</Day>
</DateCompleted>
<DateRevised><Year>2012</Year>
<Month>03</Month>
<Day>12</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1878-5883</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>315</Volume>
<Issue>1-2</Issue>
<PubDate><Year>2012</Year>
<Month>Apr</Month>
<Day>15</Day>
</PubDate>
</JournalIssue>
<Title>Journal of the neurological sciences</Title>
<ISOAbbreviation>J. Neurol. Sci.</ISOAbbreviation>
</Journal>
<ArticleTitle>Kawasaki disease complicated by mild encephalopathy with a reversible splenial lesion (MERS).</ArticleTitle>
<Pagination><MedlinePgn>167-9</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1016/j.jns.2011.11.022</ELocationID>
<Abstract><AbstractText>We reported four patients (2 to 10 years) with Kawasaki disease complicated by clinically mild encephalitis/encephalopathy with a reversible splenial lesion (MERS). All were treated with γ-globulin (2 to 6 g/kg) after the diagnosis of Kawasaki disease, the fever being alleviated between day 6 and 25. One of two patients exhibiting a poor response to γ-globulin had a cardiac aneurysm as a sequela. Their neurological manifestations (delirious behavior and drowsiness), laboratorial hyponatremia, and radiological abnormalities completely disappeared. It is important for pediatricians to acknowledge that MERS can be observed in patients with Kawasaki disease, especially in older children, and that they might be at high risk for cardiac abnormalities.</AbstractText>
<CopyrightInformation>Copyright © 2011 Elsevier B.V. All rights reserved.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Takanashi</LastName>
<ForeName>Jun-ichi</ForeName>
<Initials>J</Initials>
<AffiliationInfo><Affiliation>Department of Pediatrics, Kameda Medical Center, Kamogawa, Japan. jtaka@kameda.jp</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Shirai</LastName>
<ForeName>Kentaro</ForeName>
<Initials>K</Initials>
</Author>
<Author ValidYN="Y"><LastName>Sugawara</LastName>
<ForeName>Yuji</ForeName>
<Initials>Y</Initials>
</Author>
<Author ValidYN="Y"><LastName>Okamoto</LastName>
<ForeName>Yoko</ForeName>
<Initials>Y</Initials>
</Author>
<Author ValidYN="Y"><LastName>Obonai</LastName>
<ForeName>Toshimasa</ForeName>
<Initials>T</Initials>
</Author>
<Author ValidYN="Y"><LastName>Terada</LastName>
<ForeName>Hitoshi</ForeName>
<Initials>H</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType>
<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic"><Year>2011</Year>
<Month>11</Month>
<Day>29</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo><Country>Netherlands</Country>
<MedlineTA>J Neurol Sci</MedlineTA>
<NlmUniqueID>0375403</NlmUniqueID>
<ISSNLinking>0022-510X</ISSNLinking>
</MedlineJournalInfo>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D002648" MajorTopicYN="N">Child</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002675" MajorTopicYN="N">Child, Preschool</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D003337" MajorTopicYN="N">Corpus Callosum</DescriptorName>
<QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D004660" MajorTopicYN="N">Encephalitis</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName>
<QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D009080" MajorTopicYN="N">Mucocutaneous Lymph Node Syndrome</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName>
<QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="received"><Year>2011</Year>
<Month>08</Month>
<Day>20</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="revised"><Year>2011</Year>
<Month>11</Month>
<Day>06</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted"><Year>2011</Year>
<Month>11</Month>
<Day>08</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez"><Year>2011</Year>
<Month>12</Month>
<Day>2</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed"><Year>2011</Year>
<Month>12</Month>
<Day>2</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>2012</Year>
<Month>12</Month>
<Day>10</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">22129937</ArticleId>
<ArticleId IdType="pii">S0022-510X(11)00674-5</ArticleId>
<ArticleId IdType="doi">10.1016/j.jns.2011.11.022</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations><list><country><li>Japon</li>
</country>
</list>
<tree><noCountry><name sortKey="Obonai, Toshimasa" sort="Obonai, Toshimasa" uniqKey="Obonai T" first="Toshimasa" last="Obonai">Toshimasa Obonai</name>
<name sortKey="Okamoto, Yoko" sort="Okamoto, Yoko" uniqKey="Okamoto Y" first="Yoko" last="Okamoto">Yoko Okamoto</name>
<name sortKey="Shirai, Kentaro" sort="Shirai, Kentaro" uniqKey="Shirai K" first="Kentaro" last="Shirai">Kentaro Shirai</name>
<name sortKey="Sugawara, Yuji" sort="Sugawara, Yuji" uniqKey="Sugawara Y" first="Yuji" last="Sugawara">Yuji Sugawara</name>
<name sortKey="Terada, Hitoshi" sort="Terada, Hitoshi" uniqKey="Terada H" first="Hitoshi" last="Terada">Hitoshi Terada</name>
</noCountry>
<country name="Japon"><noRegion><name sortKey="Takanashi, Jun Ichi" sort="Takanashi, Jun Ichi" uniqKey="Takanashi J" first="Jun-Ichi" last="Takanashi">Jun-Ichi Takanashi</name>
</noRegion>
</country>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Sante/explor/MersV1/Data/Ncbi/Merge
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000904 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Ncbi/Merge/biblio.hfd -nk 000904 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Sante |area= MersV1 |flux= Ncbi |étape= Merge |type= RBID |clé= pubmed:22129937 |texte= Kawasaki disease complicated by mild encephalopathy with a reversible splenial lesion (MERS). }}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Ncbi/Merge/RBID.i -Sk "pubmed:22129937" \ | HfdSelect -Kh $EXPLOR_AREA/Data/Ncbi/Merge/biblio.hfd \ | NlmPubMed2Wicri -a MersV1
![]() | This area was generated with Dilib version V0.6.33. | ![]() |