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Updated: Jul 3, 2026

A Murine Model of Dengue Virus-induced Acute Viral Encephalitis-like Disease
Published on: April 28, 2019
Severe form of acute influenza encephalopathy with biphasic seizures and late reduced diffusion
H Tada1, J-i Takanashi, H Terada
1Department of Pediatrics, Kameda Medical Center, Kamogawa, Japan.
Abstract:
Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is clinically characterized by biphasic seizures on days 1, and 4 to 6; radiologically by no acute abnormality is visible during the first two days, while reduced diffusion in the subcortical white matter is seen during days 3 to 9, finally resulting in cerebral atrophy. We report here a Japanese child with clinically severe AESD associated with influenza A, whose sequential magnetic resonance imaging revealed cerebral swelling on day 1, reduced diffusion and central herniation on day 6, followed by cortical laminar necrosis and atrophy on day 30. The findings from this patient suggests that AESD has clinically and radiologically a wider spectrum than previously considered.
Insights
Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) presents with characteristic seizure patterns and diffusion changes. This case highlights a wider spectrum of AESD, including cerebral swelling and herniation, suggesting broader clinical and radiological variability.
Area of Science:
- Neurology
- Pediatric Neurology
- Neuroradiology
Background:
- Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is a rare neurological disorder.
- Typical AESD involves biphasic seizures and characteristic diffusion-weighted imaging findings.
Observation:
- We present a case of clinically severe AESD in a Japanese child associated with influenza A.
- Sequential magnetic resonance imaging (MRI) demonstrated cerebral swelling on day 1.
- Further imaging revealed reduced diffusion and central herniation on day 6, followed by cortical laminar necrosis and atrophy on day 30.
Findings:
- The patient exhibited a more severe and rapid progression of neurological symptoms than typically described in AESD.
- MRI findings indicated significant cerebral edema, mass effect, and subsequent ischemic changes.
- The observed timeline of radiological changes suggests a dynamic and potentially aggressive disease process.
Implications:
- This case expands the known clinical and radiological spectrum of AESD.
- It underscores the importance of early and serial neuroimaging in suspected AESD cases.
- Further research is needed to understand the full range of AESD presentations and potential therapeutic strategies.
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