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Craniopharyngioma difficulty in management
EANS Academy. ma'aya A. 09/25/19; 275324; EP04075
Dr. Alhareth ma'aya
Dr. Alhareth ma'aya

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Abstract
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Craniopharyngiomas are relatively benign (WHO grade I) neoplasms that typically arise in the sellar/suprasellar region. They account for ~1-5% of primary brain tumours, and can occur anywhere along the infundibulum (from the floor of the third ventricle, to the pituitary gland).
Craniopharyngioma management is challenging. Although histology is benign, the tumour can be clinically aggressive with local invasion and frequent recurrences. Extensive morbidity may be present at diagnosis and furthermore, occurs as a consequence of neurosurgery and radiotherapy. Hypothalamic symptoms can have a devastating effect on quality of life and may reduce life expectancy. This case highlights both the challenge of managing hyperphagia and morbid obesity and the importance of initial treatment preserving existing hypothalamic function and the need to avoid tumour recurrence and further surgery.
We will present our experience in KHCC over the last 12 years that highlights the significant morbidity associated with the diagnosis of craniopharyngioma, the sequelae of treatment with neurosurgery and radiotherapy, and the challenges for the endocrinologist in deciding an optimal care.
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