Resolution of syringomyelia and Chiari malformation after growth hormone therapy

Ashok Gupta1, Aleksander M Vitali, Ralph Rothstein

  • 1Division of Pediatric Neurosurgery, Department of Pediatric Surgery, British Columbia Children's Hospital/Children's and Women's Health Centre, 4480 Oak St, #K3-159, Vancouver, BC, Canada.

Insights

Growth hormone (GH) deficiency in premature infants may be linked to Chiari I malformation and syringomyelia. GH replacement therapy led to the resolution of syrinx and tonsillar herniation in a case study.

Area of Science:

  • Pediatric Endocrinology
  • Neuroscience
  • Developmental Biology

Background:

  • The co-occurrence of hypopituitarism, Chiari I malformation, and syringomyelia is a recently identified clinical association.
  • Previous reports predominantly featured patients with a history of perinatal injury or asphyxia.

Observation:

  • This study details a premature infant diagnosed with growth hormone (GH) deficiency, Chiari I malformation, and syringohydromyelia.
  • Notably, this patient had no identifiable history of perinatal injury.

Findings:

  • Growth hormone (GH) deficiency was identified in the premature infant.
  • Treatment with GH replacement therapy resulted in the resolution of the syrinx and tonsillar herniation.

Implications:

  • This case suggests a potential link between GH deficiency and Chiari I malformation/syringomyelia in the absence of perinatal insults.
  • GH replacement therapy may be a viable treatment option for resolving syringomyelia and tonsillar herniation in such cases.
  • Further research is warranted to elucidate the underlying mechanisms and confirm these findings in a larger cohort.
Abstract

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