Reversible posterior leukoencephalopathy syndrome in a patient with multiple system atrophy: A possible association with oral midodrine treatment
Identifieur interne : 001708 ( Istex/Checkpoint ); précédent : 001707; suivant : 001709Reversible posterior leukoencephalopathy syndrome in a patient with multiple system atrophy: A possible association with oral midodrine treatment
Auteurs : Joong-Seok Kim [Corée du Sud] ; Kwang-Soo Lee [Corée du Sud] ; Sung-Chul Lim [Corée du Sud] ; Jae-Young Ahn [Corée du Sud] ; In-Uk Song [Corée du Sud] ; Yeong-In Kim [Corée du Sud] ; Bum-Soo Kim [Corée du Sud] ; Hee-Tae Kim [Corée du Sud]Source :
- 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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ISTEX:3E05B4D045E3E11D652EDED5E31A85E6EF87F348Le document en format XML
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<front><div type="abstract" xml: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</div>
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