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Posterior Reversible Encephalopathy Syndrome in a Pediatric Intensive Care Unit: A Case Series
Beatriz Teixeira1, Vera Gonçalves2, Ana Lúcia Cardoso3
1Paediatric Department, Centro Materno Infantil do Norte, Centro Hospitalar Universitário de Santo António, Porto, PRT.
Insights
Posterior reversible encephalopathy syndrome (PRES) is a reversible brain condition. Early diagnosis and treatment of PRES, especially with co-occurring conditions, are vital for preventing lasting neurological damage.
Area of Science:
- Neurology
- Nephrology
- Hematology
Background:
- Posterior reversible encephalopathy syndrome (PRES) is a neurological condition characterized by headache, altered consciousness, seizures, and visual disturbances.
- PRES typically presents with white matter edema in the brain's parieto-occipital regions.
- Prompt diagnosis and management are critical to avoid permanent neurological deficits.
Observation:
- This study details three cases of PRES occurring alongside glomerulonephritis, Guillain-Barré syndrome, and sickle cell disease.
- All patients exhibited symptoms including systemic hypertension, seizures, and altered consciousness.
- Intensive care was required for decreased awareness or status epilepticus, necessitating mechanical ventilation.
Findings:
- The presented cases highlight the association of PRES with specific renal, neurological, and hematological disorders.
- Systemic hypertension and seizures were common clinical manifestations across all three patients.
- Aggressive management with anticonvulsants and antihypertensives was crucial for patient recovery.
Implications:
- These cases underscore the importance of considering PRES in patients with concurrent glomerulonephritis, Guillain-Barré syndrome, or sickle cell disease.
- Effective management of hypertension and seizures is key to favorable outcomes in PRES.
- The reversible nature of PRES was confirmed, with no chronic complications reported in these patients.
Abstract:
Posterior reversible encephalopathy syndrome (PRES) is a reversible clinical-radiographic abnormality. It is characterized by headache, altered consciousness, seizures, and visual disruption, in addition to characteristic white matter edema lesions in the parieto-occipital areas of the brain. Early detection and treatment are crucial to prevent irreversible damage. This paper presents the cases of three patients with PRES with concurrent diagnoses of glomerulonephritis, Guillain-Barré syndrome, and sickle cell disease. All patients experienced systemic hypertension, seizures, and altered consciousness. All patients were admitted to intensive care for decreased level of awareness or status epilepticus requiring invasive mechanical ventilation. Anticonvulsants and antihypertensive therapy were essential. No chronic complications were recorded.
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