Craniopharyngiomas in children and adults: systematic analysis of 121 cases with long‐term follow‐up
Churchill Hospital · Oxford Centre for Diabetes, Endocrinology and Metabolism · +2 more institutions
Abstract
Craniopharyngiomas account for 2-5% of all primary intracranial tumours. Despite their benign histological appearance, they are often associated with an unfavourable prognosis and their optimal treatment remains controversial.
To analyse the natural history and treatment outcome of children and adults presenting to the Departments of Paediatrics and Endocrinology with craniopharyngioma between 1964 and 2003. PATIENTS AND METHODS: The records of 121 patients (age range 2.5-83 years, 42 aged or = 16) were identified. The mean follow-up period since presentation was 103 months (8.6 years) (range 0.3-468 months). Sixteen patients underwent gross total removal (A), 3 gross total removal + radiotherapy (B), 51 partial removal (C), 33 partial removal + radiotherapy (D), 6 cyst evacuation alone (E) and 3 cyst evacuation + radiotherapy (F). The clinical, imaging and endocrinological data at presentation and during follow-up were analysed.
Citation impact
- FWCI
- 6.61
- Percentile
- 100%
- References
- 69
Authors
9- NKNiki Karavitaki
Churchill Hospital, Oxford Centre for Diabetes, Endocrinology and Metabolism
- CBClaudia Brufani
Churchill Hospital, Oxford Centre for Diabetes, Endocrinology and Metabolism
- JWJeremy Warner
John Radcliffe Hospital
- CBChristopher B. T. Adams
University of Oxford
- PRPatricia Richards
University of Oxford
Topics & keywords
- Medicine
- Craniopharyngioma
- Radiation therapy
- Natural history
- Surgery
- Presentation (obstetrics)
- Hydrocephalus
- Cyst
- Good health and well-being