The pathogenesis of Chiari I malformation and syringomyelia
Raymond F. Sekula, Gregory D. Arnone, Christine Crocker, Khaled M. Abdel Aziz, Noam Alperin
Abstract
Raymond F. Sekula, Gregory D. Arnone, Christine Crocker, Khaled M. Abdel Aziz, Noam Alperin
Abstract
OBJECTIVE: The pathogeneses of Chiari malformation type I and syringomyelia are incompletely understood. In this article, the authors attempt to review the current theories on the pathogeneses of Chiari I malformation and syringomyelia. METHODS: A literature review for articles pertaining to Chiari I malformation or syringomyelia before August 2010 was conducted; in addition, the author's own experience in treating Chiari I malformation and syringomyelia is included. RESULTS: Chiari I malformation has been defined radiographically as cerebellar tonsillar herniation or ectopia 5 mm or greater below the foramen magnum. By this narrow definition, Chiari I malformation (i.e. cerebellar tonsillar herniation or ectopia 5 mm or greater below the foramen magnum) likely encompasses a heterogeneous grouping of disorders caused by different mechanisms. Molecular and genetic studies have been helpful in furthering our understanding of Chiari I malformation. CONCLUSION: A review of the pathogeneses of Chiari I malformation and syringomyelia is reported.
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OBJECTIVE: The pathogeneses of Chiari malformation type I and syringomyelia are incompletely understood. In this article, the authors attempt to review the current theories on the pathogeneses of Chiari I malformation and syringomyelia. METHODS: A literature review for articles pertaining to Chiari I malformation or syringomyelia before August 2010 was conducted; in addition, the author's own experience in treating Chiari I malformation and syringomyelia is included. RESULTS: Chiari I malformation has been defined radiographically as cerebellar tonsillar herniation or ectopia 5 mm or greater below the foramen magnum. By this narrow definition, Chiari I malformation (i.e. cerebellar tonsillar herniation or ectopia 5 mm or greater below the foramen magnum) likely encompasses a heterogeneous grouping of disorders caused by different mechanisms. Molecular and genetic studies have been helpful in furthering our understanding of Chiari I malformation. CONCLUSION: A review of the pathogeneses of Chiari I malformation and syringomyelia is reported.
Key concepts: Syringomyelia, Foramen magnum, Chiari malformation, Medicine, Chiari I malformation, Syrinx (medicine), Anatomy, Surgery