Craniopharyngiomas in children - experience of consecutive 152 operated cases

A V Ciurea1, V Saceleanu2,3, A Mohan4,5

  • 1"Carol Davila" University School of Medicine - Department of Neurosurgery.

Acta Endocrinologica (Bucharest, Romania : 2005)
|July 21, 2020
PubMed

Insights

Surgery is the primary treatment for pediatric craniopharyngioma (CPH). A multidisciplinary approach is crucial due to potential complications, with age and tumor characteristics influencing outcomes.

Area of Science:

  • Pediatric neurosurgery
  • Oncology
  • Quality of life studies

Background:

  • Craniopharyngiomas (CPH) are rare pediatric intracranial tumors.
  • This multicenter study analyzed surgical management and quality of life in 152 children over 25 years.

Observation:

  • The pterional approach is recommended for CPH.
  • Gross-total removal (GTR) was achieved in 54.4% of cases.
  • Postoperative complications included diabetes insipidus (89.3%) and hypopituitarism (66.4%).

Findings:

  • Good Recovery (46.2%) and Moderate Disability (40.7%) were observed at 6 months post-surgery.
  • Surgery remains the main treatment option for pediatric CPH.
  • Age, tumor size, hydrocephalus, and hypothalamic dysfunction predict outcomes.

Implications:

  • A multidisciplinary approach is essential for managing CPH complications.
  • Optimizing surgical strategies can improve long-term quality of life for pediatric CPH patients.
Abstract

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