๐ง Brain tumours are the most common solid tumours in children, making up ~20% of childhood cancers.
They can occur in the cerebrum, cerebellum, brainstem, or spinal cord, producing diverse symptoms depending on location and size.
โจ Advances in imaging, neurosurgery, radiotherapy, and chemotherapy have significantly improved survival and quality of life in many children.
๐ Common Types of Paediatric Brain Tumours
- Medulloblastoma: Fast-growing tumour in the cerebellum, causing gait imbalance and raised ICP. Most common malignant brain tumour in children.
- Pilocytic Astrocytoma (low-grade astrocytoma): Usually benign, slow-growing, and often curable with surgery. Often arises in the cerebellum or optic pathway.
- Ependymoma: Originates from ependymal cells lining the ventricles; can obstruct CSF flow โ hydrocephalus.
- Brainstem Glioma: Includes DIPG, aggressive and inoperable, affecting cranial nerves, swallowing, and breathing.
- Craniopharyngioma: Benign but locally invasive tumour near the pituitary gland, leading to endocrine dysfunction and visual loss.
โ ๏ธ Symptoms (depend on location & size)
- ๐
Morning headaches (โ intracranial pressure)
- ๐คข Nausea & vomiting
- ๐ Vision or hearing changes
- ๐คธ Problems with balance or coordination
- โก Seizures
- ๐งฉ Behavioural or cognitive decline (school performance issues)
- ๐ถ In infants: bulging fontanelle, increasing head circumference
๐ Diagnosis
- Neuroimaging: MRI (preferred) ยฑ CT for acute hydrocephalus.
- Neurological exam: Cranial nerves, motor, gait, fundoscopy (papilloedema).
- Biopsy: Histology & molecular profiling guide treatment.
- Multidisciplinary team: Paediatric oncologists, neurosurgeons, radiologists, endocrinologists, neurologists.
๐ Treatment Options
- ๐ ๏ธ Surgery: Aim for maximal safe resection to relieve mass effect and obtain histology.
- โข๏ธ Radiotherapy: Effective but long-term effects (endocrine, neurocognitive) limit use in <12 years. Proton therapy is emerging to reduce toxicity.
- ๐ Chemotherapy: Used in medulloblastoma, high-grade gliomas, or to delay radiotherapy in young children.
- ๐ฏ Targeted Therapy: E.g., BRAF inhibitors for BRAF-mutant gliomas; immune checkpoint inhibitors under study.
- ๐ค Supportive Care: Dexamethasone for raised ICP, ventriculoperitoneal (VP) shunt for hydrocephalus, physiotherapy, occupational/speech therapy, school reintegration support.
๐ Prognosis
- Pilocytic astrocytoma: Excellent survival with complete excision (>90%).
- Medulloblastoma: ~70% 5-year survival with surgery + craniospinal irradiation + chemo.
- DIPG: Poor prognosis; median survival ~9โ12 months despite therapy.
- Ependymoma: Variable; outcome depends on resectability and molecular subtype.
- Craniopharyngioma: Benign but recurrent; long-term endocrine & visual morbidity common.
โ ๏ธ Complications
- Hydrocephalus โ may require VP shunt/ETV.
- Neurocognitive impairment from tumour or therapy.
- Endocrine dysfunction (growth hormone, thyroid, adrenal, puberty issues).
- Secondary malignancy post-radiotherapy.
๐ฌ Outlook & Research
- Genomic profiling โ more precise therapy.
- Trials on immunotherapy & tumour vaccines.
- Focus on reducing long-term neurocognitive & endocrine sequelae.
๐ References