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Intraspinal lipomas in infancy and childhood causing a tethered cord syndrome

D Stolke1, M Zumkeller, V Seifert

  • 1Neurosurgical Clinic, Medical School Hanover, West Germany.

Neurosurgical Review
|January 1, 1988
PubMed

Insights

This study examines 26 children with spina bifida occulta and intraspinal lipoma, highlighting surgical outcomes for tethered cord syndrome. Early intervention is crucial for managing neurological deterioration in pediatric patients.

Area of Science:

  • Pediatric Neurosurgery
  • Spinal Dysraphism
  • Neurology

Background:

  • Spina bifida occulta with intraspinal lipoma can cause tethered cord syndrome.
  • Clinical manifestations include skin lesions, foot deformities, and bladder/bowel dysfunction.
  • Diagnosis relies on advanced neuroradiological imaging.

Purpose of the Study:

  • To analyze the clinical presentation and surgical outcomes in children with spina bifida occulta and intraspinal lipoma.
  • To evaluate the efficacy of surgical intervention for tethered cord syndrome in this pediatric cohort.
  • To discuss the optimal timing for surgical intervention.

Main Methods:

  • Retrospective review of 26 pediatric patients.
  • Diagnostic imaging included myelography, CT, and MRI.
  • Surgical indications based on imaging and neurological status.

Main Results:

  • Patients presented with a range of symptoms from 1 month to 12 years of age.
  • Surgical treatment was performed based on radiological findings and clinical deterioration.
  • Outcomes of operative treatment were assessed.

Conclusions:

  • Surgical intervention is indicated for intraspinal lipoma and tethered cord syndrome in children with spina bifida occulta.
  • The timing of surgery, including prophylactic measures, is critical for preventing neurological deficits.

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