Pediatric Brain and Spine Surgery (Neurosurgery)
Congenital, skull and cerebrospinal-fluid conditions
| Condition | Symptoms and family observations | Selected investigations and care approach |
|---|---|---|
| Hydrocephalus | Increasing head size in infants, headache, vomiting, visual changes or altered behavior; presentation varies with age. | Neurological examination, head-growth review and selected ultrasound/MRI or urgent CT. The team considers a shunt or selected endoscopic treatment according to cause and anatomy. |
| Craniosynostosis | An unusual head shape caused by premature fusion of one or more skull sutures. | Craniofacial examination, selected imaging and eye/genetic assessment when indicated. Skull-shape changes have other causes; timing and surgical technique depend on age and subtype. |
| Spina bifida / myelomeningocele | A congenital spinal defect, sometimes with leg, bladder/bowel or hydrocephalus-related problems. | Neonatal/pediatric neurological assessment and selected brain/spine, urinary and orthopedic investigations. An open defect needs an urgent specialist pathway; closure does not guarantee reversal of existing nerve damage. |
| Tethered spinal cord syndrome | Progressive leg/back symptoms, gait changes or bladder/bowel dysfunction; some children have skin findings over the spine. | Neurological examination and spinal MRI, with selected urology/urodynamic review. Surgery is considered according to symptoms, anatomy and progression, with continued monitoring. |
| Chiari malformation / associated syringomyelia | Some children have no symptoms; others have headaches, weakness or swallowing/breathing concerns. | Brain/spinal MRI and neurological review, with selected flow or other studies. Observation or decompression depends on the type and clinical impact, not the MRI label alone. |
Tumors, cysts, epilepsy and injury
| Condition | Symptoms and records to discuss | Selected investigations and care approach |
|---|---|---|
| Brain and spinal cord tumors | Persistent/worsening headaches, vomiting, balance/vision changes, seizures or focal weakness; symptoms are not specific to tumors. | Neurological assessment, MRI and selected additional staging. Surgery/biopsy and tissue or molecular review when safe guide multidisciplinary care; some tumors need other treatments. |
| Arachnoid cysts | Often an incidental fluid-filled cyst; selected cases may cause pressure-related symptoms. | Specialist review of symptoms and MRI/selected CT. Many cysts are monitored; an imaging finding alone does not mean surgery will help. Drainage/fenestration or a shunt is considered selectively. |
| Drug-resistant epilepsy requiring surgical assessment | Seizures continuing despite appropriately selected medical treatment. | Neurology-led review of seizure history, video-EEG and MRI, with selected neuropsychological/functional studies. Surgery or neuromodulation requires a confirmed specialist program; seizure freedom is not guaranteed. |
| Head injury / selected traumatic brain or spinal injury | Injury followed by concerning headache, vomiting, reduced awareness, seizures or neurological change. | Urgent local assessment and risk-based imaging; CT is not required for every minor injury. Neurosurgery is considered for selected bleeding, pressure or structural injury; international travel must not delay emergency care. |
What should families prepare for the first review?
MRI, sedation and anesthesia preparation
Questions to ask before agreeing to surgery
Important reminders about hydrocephalus and shunts
Medicines, seizures and hospital communication
Care at home after an operation
Development, rehabilitation and family support
When should we seek urgent local care?
Brain tumors and ongoing specialist care
Travel, follow-up and the written proposal
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