Extrapontine myelinolysis in a 4 year old with diabetic ketoacidosis

Lalitha Sivaswamy1, Samir Karia

  • 1Department of Pediatrics and Neurology, Children's Hospital of Michigan, 390 Beaubien, Detroit, MI 48201, USA. lalithas@ameritech.net

Insights

Extrapontine and central pontine myelinolysis (EPM/CPM) are rare in children but can occur with diabetic ketoacidosis. Gradual correction of osmotic imbalances is crucial for preventing severe neurological deficits.

Area of Science:

  • Pediatric Neurology
  • Neuroscience
  • Metabolic Disorders

Background:

  • Extrapontine and central pontine myelinolysis (EPM/CPM) are rare neurological conditions.
  • Most commonly linked to rapid correction of hyponatremia, EPM/CPM also occurs in other clinical contexts.
  • Predisposing factors include alcoholism and malnutrition, making it more prevalent in adult neurology.

Observation:

  • A 4-year-old child presented with focal neurological deficits.
  • These deficits arose in the context of diabetic ketoacidosis and osmotic imbalances.
  • This represents the youngest reported case of EPM in a child with diabetic ketoacidosis.

Findings:

  • The patient experienced a remarkable recovery.
  • No significant cognitive or motor deficits were noted post-recovery.
  • The exact pathogenesis of EPM/CPM remains unclear, despite existing research.

Implications:

  • Highlights the importance of gradual serum osmolality correction in pediatric acute care.
  • Aims to reduce morbidity and mortality associated with EPM/CPM in children.
  • Emphasizes careful management of osmotic imbalances in pediatric diabetic ketoacidosis.

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