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

Overview

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 date

  • January 1, 1999

Research

keywords

  • Spinal Cord
  • Syringomyelia
  • Thoracic Vertebrae

Identity

Scopus Document Identifier

  • 0032930988

Digital Object Identifier (DOI)

  • 10.1159/000028760

PubMed ID

  • 10202308

Additional Document Info

volume

  • 30

issue

  • 1