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Posterior Reversible Encephalopathy Syndrome in Children: Case Series and Systematic Review
Tai-Heng Chen1, Wei-Chen Lin, Yong-Hao Tseng
11Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.
Insights
Posterior reversible encephalopathy syndrome (PRES) in children often presents with seizures and hypertension. Prompt diagnosis via MRI and intensive care lead to complete recovery in pediatric PRES patients.
Area of Science:
- Neurology
- Pediatrics
- Radiology
Background:
- Posterior reversible encephalopathy syndrome (PRES) is a neurological condition affecting children.
- Understanding its presentations and outcomes is crucial for timely diagnosis and management.
Purpose of the Study:
- To investigate the clinical presentations and outcomes of pediatric PRES.
- To identify key factors and common manifestations of PRES in children.
Main Methods:
- Retrospective analysis of 14 pediatric intensive care unit patients with PRES.
- Systematic review of 94 additional pediatric PRES cases from existing literature.
- Magnetic resonance imaging (MRI) for diagnosis.
Main Results:
- Common precipitating factors include hypertension (100%) and immunosuppressants (71%).
- Neurologic manifestations frequently observed are seizures (100%) and altered mental status (100%).
- All patients achieved complete clinical and radiologic recovery with intensive care.
Conclusions:
- Children presenting with seizures and hypertension should be evaluated for PRES.
- Early recognition and intensive management are vital for favorable outcomes in pediatric PRES.
- PRES should be considered in the differential diagnosis of acute encephalopathy in children.
Abstract:
To study presentations and outcome of posterior reversible encephalopathy syndrome in children, we retrospectively analyzed 14 patients admitted to our pediatric intensive care unit. We further assessed 94 additional pediatric cases from a systematic review. Our patients had a mean age of 11.6 years. Their precipitating factors were hypertension (100%), immunosuppressants (71%), antineoplastic agents (21%), and hemodialysis (14%). Initial neurologic manifestations included seizures (100%), mental change (100%), headache (79%), and visual disturbance (57%). After prompt diagnosis by magnetic resonance imaging (MRI) with intensive management, all patients had complete clinical recovery with subsequent radiologic resolution. Systemic literature review indicated that seizures (90%), hypertension (85%), and atypical neuroimaging findings (80%) are common presentations in childhood posterior reversible encephalopathy syndrome. We conclude that in children presenting with seizures and hypertension, a pediatric neurologist should consider posterior reversible encephalopathy syndrome within a comprehensive differential diagnosis of acute encephalopathy. Early recognition and intensive care are essential to ensure complete neurologic recovery in children with posterior reversible encephalopathy syndrome.
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