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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<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>
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<!--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>
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<titleInfo type="abbreviated" lang="en"><title>A Possible Association With Oral Midodrine</title>
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<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>
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<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>
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<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>
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<name type="personal"><namePart type="given">Sung‐Chul</namePart>
<namePart type="family">Lim</namePart>
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<affiliation>Department of Neurology, The Catholic University of Korea, Seoul, Korea</affiliation>
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<name type="personal"><namePart type="given">Jae‐Young</namePart>
<namePart type="family">Ahn</namePart>
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<affiliation>Department of Neurology, The Catholic University of Korea, Seoul, Korea</affiliation>
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<namePart type="family">Song</namePart>
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<affiliation>Department of Neurology, The Catholic University of Korea, Seoul, Korea</affiliation>
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<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>
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<name type="personal"><namePart type="given">Bum‐Soo</namePart>
<namePart type="family">Kim</namePart>
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<affiliation>Department of Radiology, The Catholic University of Korea, Seoul, Korea</affiliation>
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<name type="personal"><namePart type="given">Hee‐Tae</namePart>
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<affiliation>Department of Neurology, Hanyang University School of Medicine, Seoul, Korea</affiliation>
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<dateIssued encoding="w3cdtf">2007-05-15</dateIssued>
<dateCaptured encoding="w3cdtf">2006-11-03</dateCaptured>
<dateValid encoding="w3cdtf">2007-02-11</dateValid>
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<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>
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<titleInfo type="abbreviated"><title>Mov. Disord.</title>
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<topic>Brief Report</topic>
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<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>
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<detail type="issue"><caption>no.</caption>
<number>7</number>
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<extent unit="pages"><start>1043</start>
<end>1046</end>
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<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2007 Movement Disorder Society</accessCondition>
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