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Clinical, imagiological and etiological spectrum of posterior reversible encephalopathy syndrome

dc.contributor.authorPereira, PR
dc.contributor.authorPinho, J
dc.contributor.authorRodrigues, M
dc.contributor.authorRocha, J
dc.contributor.authorSousa, F
dc.contributor.authorAmorim, J
dc.contributor.authorRibeiro, M
dc.contributor.authorRocha, J
dc.contributor.authorFerreira, C
dc.date.accessioned2015-01-30T16:23:10Z
dc.date.available2015-01-30T16:23:10Z
dc.date.issued2015
dc.description.abstractObjective Analyze the cases of posterior reversible encephalopathy syndrome (PRES) admitted in a Neurology Department during an 8-year period. Method Retrospective observational study in a central hospital in the north of Portugal. Results 14 patients were identified, mean age 52.3 years. Precipitating factors included: eclampsia, isolated arterial hypertension, spinal trauma and autonomic dysreflexia, Guillain-Barré syndrome, sepsis, sarcoidosis and pulmonary cryptococcosis and drugs. Most patients presented posterior-predominant vasogenic edema lesions, however 64.2% presented frontal lesions and in 42.8% cerebellum was involved. Four patients also had acute ischemic lesions and 1 had hemorrhagic lesions. During follow-up 10 patients recovered fully, 2 recovered partially, 1 suffered a recurrence and 2 died in hospital. Conclusion PRES has many etiological factors. The terms posterior and reversible should be revised because PRES frequently involves other brain regions and it is not always reversible. PRES patients may develop life-threatening complications and mortality is not negligible.por
dc.identifier.citationArq Neuropsiquiatr. 2015;73(1):36-40.por
dc.identifier.urihttp://hdl.handle.net/10400.23/802
dc.language.isoporpor
dc.peerreviewedyespor
dc.subjectSíndrome da Leucoencefalopatia Posteriorpor
dc.titleClinical, imagiological and etiological spectrum of posterior reversible encephalopathy syndromepor
dc.title.alternativeEspectro clínico, imagiológico e etiológico da síndrome de encefalopatia posterior reversívelpor
dc.typejournal article
dspace.entity.typePublication
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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