Literature DB >> 14963755

Spontaneous resolution of a Chiari I malformation associated syringomyelia in one child.

A Guillen1, J M Costa.   

Abstract

A child with complete spontaneous resolution of a Chiari I malformation associated Syringomyelia without surgical intervention is presented. The child was followed clinically by serial magnetic resonance imaging (MRI) and remains neurologically stable after 8-years of follow-up. To our knowledge, only 6 pediatric cases with spontaneous resolution of a spinal cord syrinx documented by MRI without surgical intervention have been reported. This case is of interest in the light of the postulated theories to explain spontaneous resolution of syringomyelia.

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Year:  2004        PMID: 14963755     DOI: 10.1007/s00701-003-0177-0

Source DB:  PubMed          Journal:  Acta Neurochir (Wien)        ISSN: 0001-6268            Impact factor:   2.216


  3 in total

1.  Development of profound Chiari I malformation and cerebellar tissue loss and resolution following shunting of posterior fossa extra-axial cyst. Case report.

Authors:  Rabia Khan; Peter Oakes; R Shane Tubbs; W Jerry Oakes
Journal:  Childs Nerv Syst       Date:  2016-07-21       Impact factor: 1.475

2.  International survey on the management of Chiari 1 malformation and syringomyelia: evolving worldwide opinions.

Authors:  Ash Singhal; Alexander Cheong; Paul Steinbok
Journal:  Childs Nerv Syst       Date:  2018-03-12       Impact factor: 1.475

3.  Primary cerebellar tuberculoma in Arnold-Chiari malformation mimicking posterior cranial fossa tumor: the first report.

Authors:  Mohsen Nabiuni; Saeedeh Sarvarian
Journal:  Global Spine J       Date:  2011-12
  3 in total

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