II. Epidemiology
III. Risk Factors
- Cranial exposure to radiation
- Meningiomas
- Astrocytomas
- Glioblastoma multiforme
-
Genetic Factors
- Family History in 19% of cases overall
- Family History in 30% of Glioblastoma Multiforme
- Associated conditions
- Neurofibromatosis
- Tuberous sclerosis
- Turcot Syndrome
- Li-Fraumeni cancer syndrome
- Von Hippel Lindau
IV. Causes: Tumor types (under age 20 years)
- Supratentorial (40%)
- Astrocytoma (8-12%)
- Glioblastoma (<5%)
- Craniopharyngioma (5-8%)
- Ependymoma (3-5%)
- Choroid Plexus papilloma (2-3%)
- Pituitary tumor (<1%)
- Pineal tumor (2%)
- Meningioma (<1%)
- Infratentorial (60%)
- Medulloblastoma (18-25%)
- Cerebellar Astrocytoma (15-20%)
- Brain Stem glioma (8-10%)
- Ependymoma (4-6%)
- Schwannoma (<1%)
- Meningioma (<1%)
V. Findings
- Infants
- Failure to Thrive
- Irritability
- Older children
- CSF Outflow obstruction with Hydrocephalus and Increased Intracranial Pressure
- Common presentations
- Other presentations
- Focal neurologic deficits (e.g. Cranial Nerve palsy)
- Altered Mental Status
- First-time Seizure (13% of pediatric CNS tumor presentations)
VI. Imaging
VII. Management: Emergency Department
-
Seizures
- See Seizure Management
- Intracranial Hypertension or impending Brainstem Herniation
- See Cerebral Herniation
- May present with cushing triad (Hypertension, Bradycardia, irregular respiration pattern)
- Corticosteroids (e.g. Dexamethasone)
- Osmotic agents (Hypertonic Saline or Mannitol)
- Neurosurgery Consultation
-
ABC Management
- Supportive care to maintain normotension and normal carbon dioxide
-
Consultation and Referral
- CNS tumor evaluation and management (neurosurgery, oncology)
VIII. References
- Collyer, Huang and Seo (2026) Crit Dec Emerg Med 40(1): 26-33