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Updated: Jul 18, 2026

A Murine Model of Dengue Virus-induced Acute Viral Encephalitis-like Disease
Published on: April 28, 2019
[Influenza-associated encephalopathy with onset of prolonged convulsion: a case report]
Akiko Kondo1, Yoshiaki Saito, Yoshihiro Maegaki
1Division of Child Neurology, Institute for Neurological Sciences, Faculty of Medicine, Tottori University, Yonago, Tottori.
Insights
This case study details a child with influenza-associated encephalopathy, characterized by seizures and frontal lobe involvement. The study highlights the unique progression of brain signal changes on MRI, suggesting a specific encephalopathy type.
Area of Science:
- Neurology
- Pediatrics
- Infectious Diseases
Background:
- Influenza-associated encephalopathy (IAE) is a rare but serious complication in children.
- Early diagnosis and understanding of IAE pathogenesis are crucial for effective management.
Observation:
- A 1-year-old girl presented with prolonged febrile convulsions, drowsiness, and seizures, progressing to unconsciousness.
- Diffusion-weighted imaging (DWI) revealed evolving signal changes in the frontal white and gray matter, correlating with clinical deterioration.
- Transient choreoathetosis and oculogyric crisis were observed, followed by frontal lobe signs.
Findings:
- The patient's clinical course and MRI findings, including biphasic progression of DWI signal changes from white to gray matter, align with "status epilepticus-type acute encephalopathy."
- Normal inflammatory cytokine levels in cerebrospinal fluid during the acute phase.
- Resolution of DWI abnormalities was followed by frontal cortical atrophy.
Implications:
- This case underscores the importance of advanced neuroimaging, particularly DWI, in diagnosing and characterizing rare encephalopathies.
- While standard treatments like steroids and hypothermia were ineffective, further investigation into therapies for this specific encephalopathy subtype is warranted.
- Understanding the unique MRI progression may aid in differentiating IAE subtypes and guiding therapeutic strategies.
Abstract:
A 1-year-old girl with influenza-associated encephalopathy initially exhibited prolonged febrile convulsions and subsequent drowsiness. She became unconsciousness and experienced a cluster of seizures 4 days later. Diffusion-weighted magnetic resonance imaging (DWI) showed high signal intensity in the bilateral frontal white matter. This signal change migrated to the bifrontal cortical areas and the caudate nuclei within 10 days, when T2 elongation appeared over the gray and white matter of frontal lobes. Choreoathetosis and oculogyric crisis were transiently noted at this period. Frontal lobe signs, including the forded mouth opening response, after diminution of these movement disorders. The DWI signal change subsequently resolved and frontal cortical atrophy appeared thereafter. Levels of inflammatory cytokines in the cerebrospinal fluid were normal during the acute phase of clinical course. The biphasic clinical course with initial prolonged seizure, involvement of the frontal lobes, and the progression of signal change on DWI from white to gray matter, meets the characteristics of "status epilepticus-type acute encephalopathy" suggested by Shiomi et al. Although pentobarbital infusion, steroid pulse therapy and mild hypothermia did not show any apparent effects on the clinical course of this patient, further trial of these therapies may be warranted for the treatment of this type of encephalopathy.
Related Concept Videos
Encephalitis l: Introduction
Encephalitis ll: Pathophysiology
Seizures l: Introduction
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