Spontaneous resolution of a cervicothoracic syrinx in a child. Case report and review of the literature

Pediatr Neurosurg. 1999 Jan;30(1):43-6. doi: 10.1159/000028760.

Abstract

A child with near complete spontaneous resolution of a cervicothoracic syrinx and improvement in a Chiari type I malformation without surgical intervention is presented. The child was followed clinically with serial magnetic resonance (MR) imaging and has remained neurologically stable over an 11-year period. To our knowledge, only 3 pediatric cases of spontaneous resolution of a spinal cord syrinx as documented by MR imaging without surgical intervention have been reported. This case contributes to the literature on the natural history of syringes.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Abnormalities, Multiple
  • Adolescent
  • Arnold-Chiari Malformation / complications
  • Atrophy / pathology
  • Female
  • Humans
  • Magnetic Resonance Imaging
  • Remission, Spontaneous
  • Spinal Cord / pathology*
  • Syringomyelia / complications
  • Syringomyelia / pathology*
  • Thoracic Vertebrae / pathology*