Annals of Indian Academy of Neurology (Jan 2012)

Recurrent and atypical posterior reversible encephalopathy syndrome in a child with hypertension

  • Mustafa Komur,
  • Ali Delibas,
  • Ali Ertug Arslankoylu,
  • Cetin Okuyaz,
  • Engin Kara

DOI
https://doi.org/10.4103/0972-2327.99721
Journal volume & issue
Vol. 15, no. 3
pp. 208 – 210

Abstract

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Posterior reversible encephalopathy syndrome (PRES) is a clinical and radiologic entity with typical symptoms including headache, seizures, visual disturbance, altered mental status, vomiting, nausea and focal neurologic signs. In this article, we report recurrent and atypical PRES in a child with hypertension due to end-stage renal disease (ESRD) who was on a peritoneal dialysis program for 6 months. After the second hypertension attack, PRES findings did not recover and persisted as encephalomalacia. As far as we know, this case is the first child with ESRD who developed encephalomalacia after recurrent episodes of PRES. When a patient with a history of PRES presented with new clinical and neuroradiological findings, recurrent PRES should be considered.

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