| Literature DB >> 18354262 |
Adam C Lipson1, Richard G Ellenbogen, Anthony M Avellino.
Abstract
We present the case of a 17-month-old girl with an untreated Chiari I malformation who developed radiographic progression of syringomyelia over a 23-month period. The patient presented with initial symptoms of airway difficulties and gait ataxia, which did not progress clinically over this period of observation, despite recommendations for surgical decompression. At 17 months, there was a region of T(2) hyperintensity which progressed to become a syrinx within 3 months, enlarging over serial imaging studies. This is the first published report of radiographic progression from a 'presyrinx' state of T(2) hyperintensity to syringomyelia in a pediatric patient with untreated Chiari I malformation. Copyright (c) 2008 S. Karger AG, Basel.Entities:
Mesh:
Year: 2008 PMID: 18354262 DOI: 10.1159/000121379
Source DB: PubMed Journal: Pediatr Neurosurg ISSN: 1016-2291 Impact factor: 1.162