Chiari I malformation in children-the natural history

Ajay Chatrath1, Alexandria Marino1, Davis Taylor1

  • 1Department of Neurological Surgery, University of Virginia Health System, P.O. Box 800212, Charlottesville, VA, 22908-0711, USA.

Insights

Pediatric Chiari I malformations, with or without syringomyelia, often have a favorable natural history. Most asymptomatic children remain symptom-free, and conservative management is frequently favored.

Area of Science:

  • Neurology
  • Pediatric Neurosurgery
  • Medical Genetics

Background:

  • Chiari I malformation (CM-I) is a hindbrain structural anomaly.
  • Syringomyelia, a fluid-filled cyst within the spinal cord, can occur with CM-I.
  • Understanding the natural history of pediatric CM-I is crucial for guiding clinical management.

Purpose of the Study:

  • To review the natural history of pediatric Chiari I malformations.
  • To analyze outcomes in children with CM-I, both with and without syringomyelia.
  • To evaluate the course of asymptomatic versus symptomatic presentations.

Main Methods:

  • Literature review of case reports and series.
  • Inclusion of approximately 700 asymptomatic children without syringomyelia, 100 symptomatic children without syringomyelia, 22 asymptomatic children with syringomyelia, and 11 symptomatic children with syringomyelia.
  • Documentation of symptomatic and imaging outcomes at last follow-up.

Main Results:

  • Most asymptomatic children with CM-I without syrinx remained asymptomatic (94-95%) and did not develop syrinx (97-98%).
  • Approximately 48% of symptomatic children with CM-I without syrinx improved, with only 7% worsening; new-onset syrinx was rare (2%).
  • All 22 asymptomatic children with CM-I and syringomyelia remained asymptomatic at follow-up, with significant resolution of syrinx and tonsillar herniation.

Conclusions:

  • The natural history of asymptomatic pediatric CM-I with or without syringomyelia is more favorable than previously thought.
  • Conservative management appears to be a suitable approach for many pediatric CM-I cases.
  • Further research is needed to fully elucidate the natural history of symptomatic pediatric CM-I.
Abstract

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