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Published on: October 14, 2022
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.
Abstract:
A 13-year-old boy presented with syringomyelia associated with disproportionately large communicating fourth ventricle (DLCFV) manifesting as symptoms attributable to hydrocephalus and characteristic posterior fossa symptoms. Magnetic resonance imaging demonstrated remarkable dilation of the fourth ventricle and syringomyelia. Ventriculoperitoneal shunting completely resolved all symptoms as well as the ventricular and spinal cord abnormalities. Pre- and postoperative cine magnetic resonance imaging revealed the change of cerebrospinal fluid flow signal in the area of the foramen magnum. We concluded that the syringomyelia could be described as enlargement of the central canal with DLCFV.
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