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Case Report

Permanent Bilateral Vision Loss in Eclamptic Posterior Reversible Encephalopathy Syndrome

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Pages 243-247 | Received 22 Apr 2015, Accepted 25 Jun 2015, Published online: 11 Sep 2015
 

Abstract

Posterior reversible encephalopathy syndrome (PRES) classically consists of reversible vasogenic oedema in the posterior circulation territories, which is reversible both clinically and radiologically in the majority of patients after the control of hypertension. The authors describe a 27-year-old eclamptic patient with PRES in accelerated hypertension who revealed permanent vision loss associated with bilateral Purtscher retinopathy. One of the two competing theories that explain vasogenic brain oedema in PRES is excessive autoregulation leading to the dilation of cerebral arterial vessels, particularly in the occipito-parietal vasculatures. Dysfunction of endothelial cells that results in constriction of vessels has also been hypothesised as a cause of PRES. The concurrence of bilateral vaso-occlusive retinopathy and PRES supports the hypothesis that vasoconstriction is a more plausible mechanism of vasogenic oedema in PRES.

Declaration of interest. This paper was supported by research funds of Chonbuk National University in 2014.

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