Reversible posterior leukoencephalopathy syndrome in a patient with multiple system atrophy: A possible association with oral midodrine treatment
Identifieur interne : 003825 ( Istex/Corpus ); précédent : 003824; suivant : 003826Reversible posterior leukoencephalopathy syndrome in a patient with multiple system atrophy: A possible association with oral midodrine treatment
Auteurs : Joong-Seok Kim ; Kwang-Soo Lee ; Sung-Chul Lim ; Jae-Young Ahn ; In-Uk Song ; Yeong-In Kim ; Bum-Soo Kim ; Hee-Tae KimSource :
- Movement Disorders [ 0885-3185 ] ; 2007-05-15.
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Abstract
We describe a 51‐year‐old man with a 3‐year history of multiple system atrophy, who developed a reversible posterior leukoencephalopathy syndrome (RPLS) after receiving prescription midodrine for therapeutic treatment of orthostatic hypotension. Typical reversible magnetic resonance imaging findings, following treatment with midodrine, suggested a possible relationship between midodrine treatment, supine hypertension, and RPLS, although a cause‐and‐effect relationship cannot be confirmed. © 2007 Movement Disorder Society
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DOI: 10.1002/mds.21461
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of Korea, Seoul, Korea</mods:affiliation></affiliation></author><author><name sortKey="Ahn, Jae Oung" sort="Ahn, Jae Oung" uniqKey="Ahn J" first="Jae-Young" last="Ahn">Jae-Young Ahn</name><affiliation><mods:affiliation>Department of Neurology, The Catholic University of Korea, Seoul, Korea</mods:affiliation></affiliation></author><author><name sortKey="Song, In K" sort="Song, In K" uniqKey="Song I" first="In-Uk" last="Song">In-Uk Song</name><affiliation><mods:affiliation>Department of Neurology, The Catholic University of Korea, Seoul, Korea</mods:affiliation></affiliation></author><author><name sortKey="Kim, Yeong N" sort="Kim, Yeong N" uniqKey="Kim Y" first="Yeong-In" last="Kim">Yeong-In Kim</name><affiliation><mods:affiliation>Department of Neurology, The Catholic University of Korea, Seoul, Korea</mods:affiliation></affiliation></author><author><name sortKey="Kim, Bum Oo" sort="Kim, Bum Oo" uniqKey="Kim B" first="Bum-Soo" last="Kim">Bum-Soo 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uniqKey="Kim H" first="Hee-Tae" last="Kim">Hee-Tae Kim</name><affiliation><mods:affiliation>Department of Neurology, Hanyang University School of Medicine, Seoul, Korea</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Movement Disorders</title><title level="j" type="abbrev">Mov. 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Typical reversible magnetic resonance imaging findings, following treatment with midodrine, suggested a possible relationship between midodrine treatment, supine hypertension, and RPLS, although a cause‐and‐effect relationship cannot be confirmed. © 2007 Movement Disorder Society</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>Joong‐Seok Kim MD</name><affiliations><json:string>Department of Neurology, The Catholic University of Korea, Seoul, Korea</json:string></affiliations></json:item><json:item><name>Kwang‐Soo Lee MD</name><affiliations><json:string>Department of Neurology, The Catholic University of Korea, Seoul, Korea</json:string></affiliations></json:item><json:item><name>Sung‐Chul Lim MD</name><affiliations><json:string>Department of Neurology, The Catholic University of Korea, Seoul, Korea</json:string></affiliations></json:item><json:item><name>Jae‐Young Ahn MD</name><affiliations><json:string>Department of Neurology, The Catholic University of Korea, Seoul, Korea</json:string></affiliations></json:item><json:item><name>In‐Uk Song MD</name><affiliations><json:string>Department of Neurology, The Catholic University of Korea, Seoul, Korea</json:string></affiliations></json:item><json:item><name>Yeong‐In Kim MD</name><affiliations><json:string>Department of Neurology, The Catholic University of Korea, Seoul, Korea</json:string></affiliations></json:item><json:item><name>Bum‐Soo Kim MD</name><affiliations><json:string>Department of Radiology, The Catholic University of Korea, Seoul, Korea</json:string></affiliations></json:item><json:item><name>Hee‐Tae Kim MD</name><affiliations><json:string>Department of Neurology, Hanyang University School of Medicine, Seoul, Korea</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>reversible posterior leukoencephalopathy syndrome</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>midodrine</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>orthostatic hypotension</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>multiple system atrophy</value></json:item></subject><language><json:string>eng</json:string></language><abstract>We describe a 51‐year‐old man with a 3‐year history of multiple system atrophy, who developed a reversible posterior leukoencephalopathy syndrome (RPLS) after receiving prescription midodrine for therapeutic treatment of orthostatic hypotension. 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affiliationRef="#af2"><personName><givenNames>Bum‐Soo</givenNames><familyName>Kim</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au8" creatorRole="author" affiliationRef="#af3"><personName><givenNames>Hee‐Tae</givenNames><familyName>Kim</familyName><degrees>MD</degrees></personName></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="KR" type="organization"><unparsedAffiliation>Department of Neurology, The Catholic University of Korea, Seoul, Korea</unparsedAffiliation></affiliation><affiliation xml:id="af2" countryCode="KR" type="organization"><unparsedAffiliation>Department of Radiology, The Catholic University of Korea, Seoul, Korea</unparsedAffiliation></affiliation><affiliation xml:id="af3" countryCode="KR" type="organization"><unparsedAffiliation>Department of Neurology, Hanyang University School of Medicine, Seoul, Korea</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">reversible posterior leukoencephalopathy syndrome</keyword><keyword xml:id="kwd2">midodrine</keyword><keyword xml:id="kwd3">orthostatic hypotension</keyword><keyword xml:id="kwd4">multiple system atrophy</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>We describe a 51‐year‐old man with a 3‐year history of multiple system atrophy, who developed a reversible posterior leukoencephalopathy syndrome (RPLS) after receiving prescription midodrine for therapeutic treatment of orthostatic hypotension. Typical reversible magnetic resonance imaging findings, following treatment with midodrine, suggested a possible relationship between midodrine treatment, supine hypertension, and RPLS, although a cause‐and‐effect relationship cannot be confirmed. © 2007 Movement Disorder Society</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><!--Version 0.6 générée le 4-12-2015--><mods version="3.6"><titleInfo lang="en"><title>Reversible posterior leukoencephalopathy syndrome in a patient with multiple system atrophy: A possible association with oral midodrine treatment</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>A Possible Association With Oral Midodrine</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Reversible posterior leukoencephalopathy syndrome in a patient with multiple system atrophy: A possible association with oral midodrine treatment</title></titleInfo><name type="personal"><namePart type="given">Joong‐Seok</namePart><namePart type="family">Kim</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurology, The Catholic University of Korea, Seoul, Korea</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Kwang‐Soo</namePart><namePart type="family">Lee</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurology, The Catholic University of Korea, Seoul, Korea</affiliation><description>Correspondence: Department of Neurology, Kangnam St. Mary's Hospital, The Catholic University of Korea, 505 Banpo‐dong, Seocho‐gu, 137‐701 Seoul, Korea</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Sung‐Chul</namePart><namePart type="family">Lim</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurology, The Catholic University of Korea, Seoul, Korea</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Jae‐Young</namePart><namePart type="family">Ahn</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurology, The Catholic University of Korea, Seoul, Korea</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">In‐Uk</namePart><namePart type="family">Song</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurology, The Catholic University of Korea, Seoul, Korea</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Yeong‐In</namePart><namePart type="family">Kim</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurology, The Catholic University of Korea, Seoul, Korea</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Bum‐Soo</namePart><namePart type="family">Kim</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Radiology, The Catholic University of Korea, Seoul, Korea</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Hee‐Tae</namePart><namePart type="family">Kim</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurology, Hanyang University School of Medicine, Seoul, Korea</affiliation><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">2007-05-15</dateIssued><dateCaptured encoding="w3cdtf">2006-11-03</dateCaptured><dateValid encoding="w3cdtf">2007-02-11</dateValid><copyrightDate encoding="w3cdtf">2007</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">2</extent><extent unit="references">16</extent><extent unit="words">1540</extent></physicalDescription><abstract lang="en">We describe a 51‐year‐old man with a 3‐year history of multiple system atrophy, who developed a reversible posterior leukoencephalopathy syndrome (RPLS) after receiving prescription midodrine for therapeutic treatment of orthostatic hypotension. Typical reversible magnetic resonance imaging findings, following treatment with midodrine, suggested a possible relationship between midodrine treatment, supine hypertension, and RPLS, although a cause‐and‐effect relationship cannot be confirmed. © 2007 Movement Disorder Society</abstract><subject lang="en"><genre>Keywords</genre><topic>reversible posterior leukoencephalopathy syndrome</topic><topic>midodrine</topic><topic>orthostatic hypotension</topic><topic>multiple system atrophy</topic></subject><relatedItem type="host"><titleInfo><title>Movement Disorders</title></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>2007</date><detail type="volume"><caption>vol.</caption><number>22</number></detail><detail type="issue"><caption>no.</caption><number>7</number></detail><extent unit="pages"><start>1043</start><end>1046</end><total>4</total></extent></part></relatedItem><identifier type="istex">3E05B4D045E3E11D652EDED5E31A85E6EF87F348</identifier><identifier type="DOI">10.1002/mds.21461</identifier><identifier type="ArticleID">MDS21461</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2007 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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