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Mechanisms of cerebellar tonsil herniation in patients with Chiari malformations as guide to clinical management

BACKGROUND: The pathogenesis of Chiari malformations is incompletely understood. We tested the hypothesis that different etiologies have different mechanisms of cerebellar tonsil herniation (CTH), as revealed by posterior cranial fossa (PCF) morphology. METHODS: In 741 patients with Chiari malformat...

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Autores principales: Milhorat, Thomas H., Nishikawa, Misao, Kula, Roger W., Dlugacz, Yosef D.
Formato: Texto
Lenguaje:English
Publicado: Springer Vienna 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887504/
https://www.ncbi.nlm.nih.gov/pubmed/20440631
http://dx.doi.org/10.1007/s00701-010-0636-3
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author Milhorat, Thomas H.
Nishikawa, Misao
Kula, Roger W.
Dlugacz, Yosef D.
author_facet Milhorat, Thomas H.
Nishikawa, Misao
Kula, Roger W.
Dlugacz, Yosef D.
author_sort Milhorat, Thomas H.
collection PubMed
description BACKGROUND: The pathogenesis of Chiari malformations is incompletely understood. We tested the hypothesis that different etiologies have different mechanisms of cerebellar tonsil herniation (CTH), as revealed by posterior cranial fossa (PCF) morphology. METHODS: In 741 patients with Chiari malformation type I (CM-I) and 11 patients with Chiari malformation type II (CM-II), the size of the occipital enchondrium and volume of the PCF (PCFV) were measured on reconstructed 2D-CT and MR images of the skull. Measurements were compared with those in 80 age- and sex-matched healthy control individuals, and the results were correlated with clinical findings. RESULTS: Significant reductions of PCF size and volume were present in 388 patients with classical CM-I, 11 patients with CM-II, and five patients with CM-I and craniosynostosis. Occipital bone size and PCFV were normal in 225 patients with CM-I and occipitoatlantoaxial joint instability, 55 patients with CM-I and tethered cord syndrome (TCS), 30 patients with CM-I and intracranial mass lesions, and 28 patients with CM-I and lumboperitoneal shunts. Ten patients had miscellaneous etiologies. The size and area of the foramen magnum were significantly smaller in patients with classical CM-I and CM-I occurring with craniosynostosis and significantly larger in patients with CM-II and CM-I occurring with TCS. CONCLUSIONS: Important clues concerning the pathogenesis of CTH were provided by morphometric measurements of the PCF. When these assessments were correlated with etiological factors, the following causal mechanisms were suggested: (1) cranial constriction; (2) cranial settling; (3) spinal cord tethering; (4) intracranial hypertension; and (5) intraspinal hypotension.
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spelling pubmed-28875042010-07-12 Mechanisms of cerebellar tonsil herniation in patients with Chiari malformations as guide to clinical management Milhorat, Thomas H. Nishikawa, Misao Kula, Roger W. Dlugacz, Yosef D. Acta Neurochir (Wien) Clinical Article BACKGROUND: The pathogenesis of Chiari malformations is incompletely understood. We tested the hypothesis that different etiologies have different mechanisms of cerebellar tonsil herniation (CTH), as revealed by posterior cranial fossa (PCF) morphology. METHODS: In 741 patients with Chiari malformation type I (CM-I) and 11 patients with Chiari malformation type II (CM-II), the size of the occipital enchondrium and volume of the PCF (PCFV) were measured on reconstructed 2D-CT and MR images of the skull. Measurements were compared with those in 80 age- and sex-matched healthy control individuals, and the results were correlated with clinical findings. RESULTS: Significant reductions of PCF size and volume were present in 388 patients with classical CM-I, 11 patients with CM-II, and five patients with CM-I and craniosynostosis. Occipital bone size and PCFV were normal in 225 patients with CM-I and occipitoatlantoaxial joint instability, 55 patients with CM-I and tethered cord syndrome (TCS), 30 patients with CM-I and intracranial mass lesions, and 28 patients with CM-I and lumboperitoneal shunts. Ten patients had miscellaneous etiologies. The size and area of the foramen magnum were significantly smaller in patients with classical CM-I and CM-I occurring with craniosynostosis and significantly larger in patients with CM-II and CM-I occurring with TCS. CONCLUSIONS: Important clues concerning the pathogenesis of CTH were provided by morphometric measurements of the PCF. When these assessments were correlated with etiological factors, the following causal mechanisms were suggested: (1) cranial constriction; (2) cranial settling; (3) spinal cord tethering; (4) intracranial hypertension; and (5) intraspinal hypotension. Springer Vienna 2010-05-04 2010 /pmc/articles/PMC2887504/ /pubmed/20440631 http://dx.doi.org/10.1007/s00701-010-0636-3 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Clinical Article
Milhorat, Thomas H.
Nishikawa, Misao
Kula, Roger W.
Dlugacz, Yosef D.
Mechanisms of cerebellar tonsil herniation in patients with Chiari malformations as guide to clinical management
title Mechanisms of cerebellar tonsil herniation in patients with Chiari malformations as guide to clinical management
title_full Mechanisms of cerebellar tonsil herniation in patients with Chiari malformations as guide to clinical management
title_fullStr Mechanisms of cerebellar tonsil herniation in patients with Chiari malformations as guide to clinical management
title_full_unstemmed Mechanisms of cerebellar tonsil herniation in patients with Chiari malformations as guide to clinical management
title_short Mechanisms of cerebellar tonsil herniation in patients with Chiari malformations as guide to clinical management
title_sort mechanisms of cerebellar tonsil herniation in patients with chiari malformations as guide to clinical management
topic Clinical Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887504/
https://www.ncbi.nlm.nih.gov/pubmed/20440631
http://dx.doi.org/10.1007/s00701-010-0636-3
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