[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.

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