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Recurrent and atypical posterior reversible encephalopathy syndrome in a child with hypertension
Mustafa Komur1, Ali Delibas, Ali Ertug Arslankoylu
1Department of Pediatric Neurology, Mersin University School of Medicine, Mersin, Turkey.
Insights
Posterior reversible encephalopathy syndrome (PRES) can lead to permanent brain damage (encephalomalacia) in children with end-stage renal disease (ESRD). Recurrent PRES episodes in ESRD patients require careful monitoring to prevent irreversible neurological deficits.
Area of Science:
- Neurology
- Nephrology
- Pediatrics
Background:
- Posterior reversible encephalopathy syndrome (PRES) is a neurological condition characterized by headache, seizures, and visual disturbances.
- End-stage renal disease (ESRD) often leads to hypertension, a known risk factor for PRES.
Observation:
- This case report details a child with ESRD on peritoneal dialysis who experienced recurrent PRES.
- Following a second hypertensive crisis, the PRES findings in this patient did not resolve and progressed to encephalomalacia.
Findings:
- This represents the first reported case of a child with ESRD developing encephalomalacia secondary to recurrent PRES.
- The persistent PRES findings highlight the potential for irreversible brain injury in this vulnerable population.
Implications:
- Clinicians should consider recurrent PRES in ESRD patients presenting with new neurological symptoms.
- Early recognition and management of hypertension are crucial to prevent PRES progression and irreversible neurological damage in pediatric ESRD patients.
Abstract:
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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