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Published on: November 20, 2015
Posterior reversible encephalopathy syndrome in a child with leptospira-associated glomerulonephritis: the 3 P'S
Bing Chan Shu1, Caisha Moses2,3
1Emergency Department, Sarawak General Hospital, Kuching, Malaysia.
Insights
Posterior reversible encephalopathy syndrome (PRES) can be mistaken for infections in children. Early recognition using the '3 P's' framework (Pressure, Pattern, Pictures) aids timely treatment for better outcomes.
Area of Science:
- Neurology
- Pediatrics
- Infectious Diseases
Background:
- Posterior reversible encephalopathy syndrome (PRES) is an under-recognized cause of pediatric seizures.
- PRES is often misdiagnosed, particularly when co-occurring with infections.
Purpose of the Study:
- To report a case of PRES secondary to leptospira-associated glomerulonephritis in a child.
- To highlight the diagnostic challenge posed by anchoring bias in PRES.
- To introduce a practical framework for early PRES recognition and management.
Main Methods:
- Case report of a middle childhood girl with recurrent seizures after fever and flood exposure.
- Diagnostic workup included serology, blood pressure monitoring, and CT brain imaging.
- Treatment involved antihypertensives, antiepileptics, and antibiotics.
Main Results:
- Initial diagnosis was leptospira encephalitis, but progressive hypertension and CT findings confirmed PRES.
- PRES was secondary to leptospira-associated acute glomerulonephritis.
- The patient improved with treatment and was discharged seizure-free.
Conclusions:
- Leptospira infection can precipitate PRES via acute glomerulonephritis.
- Anchoring bias can delay PRES diagnosis.
- The '3 P's' (Pressure, Pattern, Pictures) framework can improve PRES recognition and management in children.
Abstract:
Posterior reversible encephalopathy syndrome (PRES) is an under-recognised cause of seizures in children, often obscured by concurrent infections. We report a girl in her middle childhood with recurrent seizures following a week of fever and flood exposure. Initial suspicion was leptospira encephalitis, supported by positive serology. However, progressive hypertension and CT brain findings confirmed PRES secondary to leptospira-associated acute glomerulonephritis. She improved with antihypertensives, antiepileptics and antibiotics, and was discharged seizure-free. This case highlights the risk of anchoring bias and introduces the '3 P's of PRES' framework-Pressure, Pattern and Pictures-for earlier recognition and management.
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