Disproportionately large communicating fourth ventricle with syringomyelia: case report

Naoshi Hagihara1, Shuji Sakata

  • 1Department of Neurosurgery, Saga Prefectural Hospital Kouseikan, Morodomi-cho,Saga, Japan. hagihan@post.saga-med.ac.jp

Insights

Syringomyelia in a boy was linked to a large communicating fourth ventricle. Ventriculoperitoneal shunting resolved hydrocephalus, posterior fossa symptoms, and spinal cord abnormalities, indicating a connection between these conditions.

Area of Science:

  • Pediatric Neurology
  • Neurosurgery
  • Neuroimaging

Background:

  • Syringomyelia is a rare condition characterized by a fluid-filled cyst within the spinal cord.
  • Hydrocephalus involves excess cerebrospinal fluid in the brain, leading to increased pressure.
  • Posterior fossa symptoms can arise from structural abnormalities in the lower part of the brain.

Observation:

  • A 13-year-old male presented with syringomyelia and a disproportionately large communicating fourth ventricle (DLCFV).
  • Clinical manifestations included symptoms of hydrocephalus and typical posterior fossa signs.
  • Magnetic resonance imaging (MRI) revealed significant fourth ventricular dilation and syringomyelia.

Findings:

  • Ventriculoperitoneal shunting effectively resolved all presenting symptoms.
  • Post-shunt placement, MRI demonstrated resolution of ventricular and spinal cord abnormalities.
  • Cine MRI before and after surgery showed altered cerebrospinal fluid flow at the foramen magnum.

Implications:

  • This case suggests DLCFV can cause or be associated with syringomyelia.
  • Ventriculoperitoneal shunting is an effective treatment for this specific combination of conditions.
  • Understanding cerebrospinal fluid dynamics is crucial for managing syringomyelia associated with fourth ventricular dilation.