What is the incidence of brain teratomas in pediatric patients?

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Incidence of Brain Teratomas in Pediatric Patients

Brain teratomas are rare in pediatric patients, accounting for less than 1% of all intracranial tumors in children, with estimates ranging from 0.5% to 2-4% of pediatric brain tumors. 1, 2

Epidemiologic Data

The incidence of intracranial teratomas in the pediatric population is notably low:

  • Teratomas represent <1% of intracranial masses during childhood after infancy 3
  • Among all pediatric brain tumors, intracranial teratomas account for 0.5% of all intracranial tumors and 2-4% of intracranial tumors specifically in children 2
  • Congenital brain tumors (presenting within 60 days of birth) are extremely rare, accounting for only 0.5-1.9% of all pediatric brain tumors, with teratoma being the most common type in this age group 4, 5

Age Distribution and Clinical Context

The age distribution shows specific patterns:

  • Most pediatric intracranial teratomas occur in the first decade of life, with a smaller proportion in the second decade 2
  • The mean age at diagnosis is approximately 10.5 years 1
  • When teratomas present congenitally (within the first 2 months of life), they represent the most frequently encountered intracranial tumor at birth, though this subset remains exceedingly rare 4, 5

Anatomic Location Patterns

Understanding tumor location helps contextualize the rarity:

  • The third ventricle (particularly posterior third ventricle) is the most common intracranial site for pediatric teratomas 2
  • Suprasellar and pineal regions are also common locations when teratomas occur supratentorially 3
  • Teratomas located in the posterior third ventricle are more likely to contain immature components 2

Clinical Significance

Despite their rarity, recognition is important because:

  • Intracranial teratomas are classified as a rare subset of primary intracranial non-germinomatous germ cell tumors (NGGCT) 1
  • The prognosis for mature teratomas is excellent, with no recurrences reported in recent case series with median follow-up of 4.6 years 1
  • Common long-term sequelae include endocrine abnormalities (42.8%) and eye movement abnormalities (50.0%) 1

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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