dc.creatorHernández Ch,Marta
dc.creatorNúñez F,Alicia
dc.creatorMesa L,Tomas
dc.creatorEscobar H,Raúl
dc.creatorBarriga C,Francisco
dc.creatorHuete L,Isidro
dc.date2008-01-01
dc.date.accessioned2017-03-07T16:00:34Z
dc.date.available2017-03-07T16:00:34Z
dc.identifierhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872008000100012
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/394457
dc.descriptionReversible posterior leukoencephalopathy syndrome (PLS) is characterized by headache, clouding of sensorium, visual disturbances and seizures. It is associated to hypertension, renal disease or immunosuppressive therapy. We report three males, aged 9, 12 and 16 years and one female, aged 5 years wih PLS associated to immunosuppressive therapy. All had seizures and three had headache and clouding of sensorium. One case was associated to an hypertensive emergency, one to liver failure and one to high tacrolimus levels. Magnetic resonance imaging showed lesions in the white matter in two patients and in the gray matter in the other two. The lapse between the start of immunosuppressive treatment and neurological symptoms ranged from 4 days to 6 months. All received antiepileptic drugs and immunosuppresive therapy was changed or decreased, with complete clinical recovery (Rev Méd Chile 2008, 136: 93-8)
dc.formattext/html
dc.languagees
dc.publisherSociedad Médica de Santiago
dc.sourceRevista médica de Chile v.136 n.1 2008
dc.subjectImmunosupression
dc.subjectPosterior leukoencephalopathy syndrome
dc.subjectTacrolimus
dc.titleLeucoencefalopatía reversible posterior: cuatro casos clínicos
dc.typeArtículos de revistas


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