Full recovery of adult onset opsoclonus myoclonus syndrome after early immunotherapy: A case report
Identifieur interne : 003C74 ( Istex/Corpus ); précédent : 003C73; suivant : 003C75Full recovery of adult onset opsoclonus myoclonus syndrome after early immunotherapy: A case report
Auteurs : Stefan J. Groiss ; Mario Siebler ; Alfons SchnitzlerSource :
- Movement Disorders [ 0885-3185 ] ; 2011-08-15.
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DOI: 10.1002/mds.23854
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Clinical long‐term follow‐up for 28 months. Segment 1 (0:00): complete clinical picture of opsoclonus‐myoclonus syndrome (OMS) before initiating corticosteroid therapy. The patient is not able to stand or walk as a result of marked generalized myoclonus. Segment 2 (0:24): Four weeks later, after treatment with corticosteroids. Opsoclonus has improved and myoclonus has markedly decreased. The patient is able to stand with assistance. Segment 3 (0:49): Six months after onset of symptoms. The patient has recovered from OMS and walks fluently without help. At this time, antineoplastic treatment was not yet initiated. The carcinoma was removed 1 week later. Segment 4 (1:10): Long‐term follow‐up 28 months after symptom onset. Symptoms are remittent without any relapse.</caption></supportingInfoItem></supportingInformation></contentMeta><noteGroup><note xml:id="fn1"><p>Relevant conflicts of interest/financial disclosures: Nothing to report.</p></note><note xml:id="fn2"><p>Full financial disclosures and author roles may be found in the online version of this article.</p></note></noteGroup></header></component></istex:document></istex:metadataXml><!--Version 0.6 générée le 4-12-2015--><mods version="3.6"><titleInfo lang="en"><title>Full recovery of adult onset opsoclonus myoclonus syndrome after early immunotherapy: A case report</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Full recovery of adult onset opsoclonus myoclonus syndrome after early immunotherapy: A case report</title></titleInfo><name type="personal"><namePart type="given">Stefan J.</namePart><namePart type="family">Groiss</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Institute of Clinical Neuroscience and Medical Psychology, Heinrich‐Heine‐University Düsseldorf, Düsseldorf, Germany</affiliation><affiliation>Department of Neurology, Heinrich‐Heine‐University Düsseldorf, Düsseldorf, Germany</affiliation><affiliation>Current Address: Department of Neurology, Fukushima Medical University, School of Medicine, Fukushima, Japan</affiliation><description>Correspondence: Department of Neurology, Fukushima Medical University, School of Medicine, 1 Hikarigaoka, 960‐1295 Fukushima, Japan</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Mario</namePart><namePart type="family">Siebler</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurology, Heinrich‐Heine‐University Düsseldorf, Düsseldorf, Germany</affiliation><affiliation>Department of Neurology, MediClin Rehabilitation Clinic Rhein/Ruhr, Essen, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Alfons</namePart><namePart type="family">Schnitzler</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Institute of Clinical Neuroscience and Medical Psychology, Heinrich‐Heine‐University Düsseldorf, Düsseldorf, Germany</affiliation><affiliation>Department of Neurology, Heinrich‐Heine‐University Düsseldorf, Düsseldorf, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre authority="originalCategForm">miscellaneous</genre><originInfo><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><place><placeTerm type="text">Hoboken</placeTerm></place><dateIssued encoding="w3cdtf">2011-08-15</dateIssued><dateCaptured encoding="w3cdtf">2011-03-09</dateCaptured><dateValid encoding="w3cdtf">2011-05-16</dateValid><copyrightDate encoding="w3cdtf">2011</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="references">11</extent><extent unit="words">1831</extent></physicalDescription><note type="content">*Relevant conflicts of interest/financial disclosures: Nothing to report.</note><note type="content">*Full financial disclosures and author roles may be found in the online version of this article.</note><relatedItem type="host"><titleInfo><title>Movement Disorders</title></titleInfo><titleInfo type="abbreviated"><title>Mov. Disord.</title></titleInfo><note type="content"> Additional Supporting Information may be found in the online version of this article.Supporting Info Item: Supporting Information Video 1. Clinical long‐term follow‐up for 28 months. Segment 1 (0:00): complete clinical picture of opsoclonus‐myoclonus syndrome (OMS) before initiating corticosteroid therapy. The patient is not able to stand or walk as a result of marked generalized myoclonus. Segment 2 (0:24): Four weeks later, after treatment with corticosteroids. Opsoclonus has improved and myoclonus has markedly decreased. The patient is able to stand with assistance. Segment 3 (0:49): Six months after onset of symptoms. The patient has recovered from OMS and walks fluently without help. At this time, antineoplastic treatment was not yet initiated. The carcinoma was removed 1 week later. Segment 4 (1:10): Long‐term follow‐up 28 months after symptom onset. Symptoms are remittent without any relapse. - </note><subject><genre>article category</genre><topic>Clinical Vignettes</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>2011</date><detail type="volume"><caption>vol.</caption><number>26</number></detail><detail type="issue"><caption>no.</caption><number>10</number></detail><extent unit="pages"><start>1805</start><end>1807</end><total>3</total></extent></part></relatedItem><identifier type="istex">76F84243B1D4A0A77B1AFF92224F195FD085F47B</identifier><identifier type="DOI">10.1002/mds.23854</identifier><identifier type="ArticleID">MDS23854</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2011 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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