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Tussive presentation in cervicomedullary junction malformations
L D Kramer1, G E Locke, S C Rasmus
1Urban Comprehensive Epilepsy Program, Institute of Neurological Sciences, Los Angeles, California.
Spine
|June 1, 1990
Summary
Craniocervical junction malformations can cause sudden, permanent neurological deficits, often triggered by coughing. These cases highlight compression and shear stress as potential injury mechanisms in the brainstem and spinal cord.
Area of Science:
- Neurology
- Neurosurgery
- Medical Imaging
Background:
- Craniocervical junction malformations are complex anatomical abnormalities at the base of the skull and top of the spine.
- These malformations can lead to significant neurological deficits due to structural abnormalities and pressure effects.
Observation:
- Two adult patients with craniocervical junction malformations experienced acute onset of permanent neurological symptoms following coughing.
- One patient presented with basilar invagination and tonsillar herniation; the other had a Type 1 Arnold-Chiari malformation with cord widening.
Findings:
- The study suggests two primary mechanisms for neurological injury in these cases: external compression of cervicomedullary structures and parenchymal shear stress.
- Posterior fossa tissue descent through the foramen magnum, potentially due to increased intracranial pressure, can cause compression.
- Caudal repositioning of neural structures can induce shear stress on the brainstem and spinal cord.
Implications:
- Understanding these mechanisms is crucial for diagnosing and managing patients with craniocervical junction malformations.
- Early recognition and intervention may help prevent permanent neurological damage in susceptible individuals.
- Further research into the biomechanics of coughing in relation to these malformations is warranted.