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Syringobulbia. Mark R. Lee, MD, PhD Pediatric Neurosurgery Dell Children’s Medical Center. Syringobulbia. Very rare entity Slit-like fluid cavity in brainstem Associated with Chiari malformation Tumors Tethered cord Idiopathic. Syringobulbia and Chiari Malformation.
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Syringobulbia Mark R. Lee, MD, PhD Pediatric Neurosurgery Dell Children’s Medical Center
Syringobulbia • Very rare entity • Slit-like fluid cavity in brainstem • Associated with • Chiari malformation • Tumors • Tethered cord • Idiopathic
Syringobulbia and Chiari Malformation • Strongly associated with Chiari malformation with syringomyelia • But very rare… • 3-5% of patients with Chiari malformation
Symptoms • Head and neck pain • Snoring • Diplopia • Sensory disturbances • Unsteady gait • Dysphagia • Paresthesias and numbness
Clinical Findings • Cranial nerve deficits • All patients • Unilateral not uncommon • Nystagmus • Weakness • Hyperreflexia • Scoliosis
Treatment • Restore CSF pathways between cranial and spinal compartments • Decompression of craniovertebral junction • Posterior fossa decompression • Suboccipital craniectomy • C1 laminectomy • Duraplasty (or dural splitting)
Syringobulbia in a pediatric population. Neurosurgery, 2005Greenlee, Menezes, et. al
What Causes Syringobulbia? • “Always” associated with syringomyelia • Propagation of syringomyelia into brainstem. • “rupture” of cervical syrinx • Extension of dilated central canal • Direct entry of CSF into brainstem • “opening” in floor of 4th ventricle
Summary • Syringobulbia is rare • Associated with syringomyelia • ? Extension of syringomyelia • Has cranial nerve dysfunction • Treated with craniovertebral decompression • Outcomes are usually good