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Published in: Journal of Neurology 8/2017

Open Access 01-08-2017 | Review

Posterior reversible encephalopathy syndrome

Authors: Marlene Fischer, Erich Schmutzhard

Published in: Journal of Neurology | Issue 8/2017

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Abstract

The posterior reversible encephalopathy syndrome (PRES) is a neurological disorder of (sub)acute onset characterized by varied neurological symptoms, which may include headache, impaired visual acuity or visual field deficits, disorders of consciousness, confusion, seizures, and focal neurological deficits. In a majority of patients the clinical presentation includes elevated arterial blood pressure up to hypertensive emergencies. Neuroimaging, in particular magnetic resonance imaging, frequently shows a distinctive parieto-occipital pattern with a symmetric distribution of changes reflecting vasogenic edema. PRES frequently develops in the context of cytotoxic medication, (pre)eclampsia, sepsis, renal disease or autoimmune disorders. The treatment is symptomatic and is determined by the underlying condition. The overall prognosis is favorable, since clinical symptoms as well as imaging lesions are reversible in most patients. However, neurological sequelae including long-term epilepsy may persist in individual cases.
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Metadata
Title
Posterior reversible encephalopathy syndrome
Authors
Marlene Fischer
Erich Schmutzhard
Publication date
01-08-2017
Publisher
Springer Berlin Heidelberg
Published in
Journal of Neurology / Issue 8/2017
Print ISSN: 0340-5354
Electronic ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-016-8377-8

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