Abstract

The exact pathogenesis of syringomyelia is unknown. Epidural venous distention during raised intrathoracic pressure (Valsalva) may cause impulsive movement of fluid (“slosh”) within the syrinx. Such a slosh mechanism is a proposed cause of syrinx dissection into spinal cord parenchyma resulting in craniocaudal propagation of the cavity. We sought to test the “slosh” hypothesis by epidural excitation of CSF pulse in a computer model of canine syringomyelia. Our previously developed canine syringomyelia computer model was modified to include an epidural pressure pulse. Simulations were run for: cord free of cavities; cord with small syringes at different locations; and cord with a syrinx that was progressively expanding caudally. If small syringes are present, there are peaks of stress at those locations. This effect is most pronounced at the locations at which syringes initially form. When a syrinx is expanding caudally, the peak stress is typically at the caudal end of the syrinx. However, when the syrinx reaches the lumbar region; the stress becomes moderate. The findings support the “slosh” hypothesis, suggesting that small cervical syringes may propagate caudally. However, when the syrinx is large, there is less focal stress, which may explain why a syrinx can rapidly expand but then remain unchanged in shape over years.

Highlights

  • 1 mm thick slices the spinaldiscussed, cord was the used as a measure alonginthe length of slices of the spinal cord was used as a measure of stress magnitude along the length of thea the spinal cord

  • The results of this study strongly suggest that the spinal cord tissue in the vicinity of fluid-filled cavities experiences higher than normal mechanical stress due to the movement of the cerebrospinal fluid (CSF) from epidural excitation

  • This study addresses syringomyelia in dogs, and in cavalier King Charles spaniel (CKCS)

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Summary

Introduction

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. Syringomyelia was first described by Stephanus in 1545; over 400 years later, the mechanism by which the spinal cord cavities (syrinx; syringes) form and fill with fluid is still debated. Syringomyelia occurs secondary to cerebrospinal fluid (CSF). The compromise in patient quality of life is comparable with that of patients with heart failure [3]. Disruption of CSF flow at the craniocervical junction increases risk of syringomyelia. Morphological changes to the skull, cervical vertebrae, and brain-to-cranial cavity ratio commonly referred to as Chiari malformation can alter dynamics of CSF flow at the craniocervical junction and is the most common cause of syringomyelia. Chiari malformation and syringomyelia affect both humans and animals

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