Treatment-associated posterior reversible encephalopathy syndrome in an adolescent with Crohn's disease: A case report
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Updated: Jan 17, 2026

Induction and Clinical Scoring of Chronic-Relapsing Experimental Autoimmune Encephalomyelitis
Published on: July 4, 2007
Manuel Feuerstein1, Micaela Salas Victoria1, Cynthia Slaifstein1
1Unit 6 Pediatric Clinic, Hospital General de Niños Ricardo Gutiérrez, Autonomous City of Buenos Aires, Argentina.
Abstract:
Posterior reversible encephalopathy syndrome (PRES) is a type of leukoencephalopathy that usually presents symptoms such as headache, altered consciousness, seizures, blurred vision, and imaging signs such as subcortical white matter edema, predominantly in the parieto-occipital lobes. Numerous risk factors have been identified, which involve impaired cerebral blood flow autoregulation and vasogenic edema. We present the case of a 14-year-old female patient who, in the context of an induction treatment for Crohn's disease with high-dose corticosteroids, azathioprine, and infliximab, presented with posterior reversible encephalopathy, a rare complication in patients with inflammatory bowel disease.
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