Natural history of Chiari type I malformation in children

Luca Massimi, Massimo Caldarelli, Paolo Frassanito, Concezio Di Rocco

Research output: Contribution to journalArticle

25 Citations (Scopus)

Abstract

The decision on whether or not to operate children with Chiari type I malformation (CIM) is difficult and controversial, because of the lack of information about the natural evolution of such a disease. Herein, we report on the evolution of 16 asymptomatic children with incidentally diagnosed CIM (mean age: 6.7 years; mean follow-up: 5.8 years). No patients required suboccipital decompression. Thirteen children remained asymptomatic, with stable or improved radiological picture (worsening in 2 cases). Three cases showed appearance of symptoms: one did not require any treatment; the remaining two underwent endoscopic third ventriculostomy because of hydrocephalus, which is a possible consequence of CIM. This analysis shows a favorable natural outcome of CIM in children, thus suggesting a conservative management in asymptomatic cases. However, multicentric studies are required to validate this data.
Original languageEnglish
Pages (from-to)S275-S275-7
JournalNeurological Sciences
Volume32 Suppl 3
DOIs
Publication statusPublished - 2011

Keywords

  • Adolescent
  • Arnold-Chiari Malformation
  • Child
  • Child, Preschool
  • Decompression, Surgical
  • Female
  • Humans
  • Infant
  • Longitudinal Studies
  • Male
  • Retrospective Studies

Fingerprint Dive into the research topics of 'Natural history of Chiari type I malformation in children'. Together they form a unique fingerprint.

Cite this