Abstract

This work is a modified version of the Casey Holter Memorial prize essay presented to the Society for Research into Hydrocephalus and Spina Bifida, June 29th 2007, Heidelberg, Germany. It describes the origin and consequences of the Chiari malformation, and proposes that hydrocephalus is caused by inadequate central nervous system (CNS) venous drainage. A new hypothesis regarding the pathogenesis, anencephaly and spina bifida is described.Any volume increase in the central nervous system can increase venous pressure. This occurs because veins are compressible and a CNS volume increase may result in reduced venous blood flow. This has the potential to cause progressive increase in cerebrospinal fluid (CSF) volume. Venous insufficiency may be caused by any disease that reduces space for venous volume. The flow of CSF has a beneficial effect on venous drainage. In health it moderates central nervous system pressure by moving between the head and spine. Conversely, obstruction to CSF flow causes localised pressure increases, which have an adverse effect on venous drainage.The Chiari malformation is associated with hindbrain herniation, which may be caused by low spinal pressure relative to cranial pressure. In these instances, there are hindbrain-related symptoms caused by cerebellar and brainstem compression. When spinal injury occurs as a result of a Chiari malformation, the primary pathology is posterior fossa hypoplasia, resulting in raised spinal pressure. The small posterior fossa prevents the flow of CSF from the spine to the head as blood enters the central nervous system during movement. Consequently, intermittent increases in spinal pressure caused by movement, result in injury to the spinal cord. It is proposed that posterior fossa hypoplasia, which has origins in fetal life, causes syringomyelia after birth and leads to damage to the spinal cord in spina bifida. It is proposed that hydrocephalus may occur as a result of posterior fossa hypoplasia, where raised pressure occurs as a result of obstruction to flow of CSF from the head to the spine, and cerebral injury with raised pressure occurs in anencephaly by this mechanism.The current view of dysraphism is that low central nervous system pressure and exposure to amniotic fluid, damage the central nervous system. The hypothesis proposed in this essay supports the view that spina bifida is a manifestation of progressive hydrocephalus in the fetus. It is proposed that that mesodermal growth insufficiency influences both neural tube closure and central nervous system pressure, leading to dysraphism.

Highlights

  • Hydrocephalus involves degrees of raised central nervous system (CNS) pressure and extracellular fluid accumulation

  • The Chiari II malformation is found in association with spina bifida and is thought by many to be unrelated to Chiari I, with neural injury and reduced posterior fossa size caused by failure of neural tube closure and its consequences, including toxicity caused by exposure to amniotic fluid [3,4]

  • Chiari-related syringomyelia, spina bifida and anencephaly form a spectrum of disease related to restricted growth of the posterior fossa

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Summary

Introduction

Hydrocephalus involves degrees of raised central nervous system (CNS) pressure and extracellular fluid accumulation. Pressure waves generated by venous volume fluctuation in the spine may influence lateral ventricle wall tension without the requirement for flow [42], so physical movement may maintain or increase ventricle size when posterior fossa CSF pathways are patent. As overall brain (including fluid) volume increases, CSF may be displaced from the subarachnoid spaces into the spine and the hindbrain may be displaced towards the foramen magnum This may enhance the rate of intracerebral pressure increase by preventing the normal to and fro flow movement of CSF across the foramen magnum [44] that facilitates CNS venous drainage.

Conclusion
Levine DN
Williams B
10. Levick RJ: An introduction to cardiovascular physiology London
14. Williams B
19. Bateman G
23. Milhorat TH: Cerebrospinal Fluid and the Brain Edemas New York
30. Marin-Padilla M
33. Williams B
63. Williams B
68. Williams H
71. Welch K
79. Williams B

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