Abstract
Craniopharyngiom as are rare epithelial tumors, arising from the pituitary gland or pituitary gland and developing in the sellar and supra sellar region. Their diagnosis is often late and is based on the triad of neurological, ophthalmological and endocrine signs. Their treatment is multidisciplinary and includes surgical and hormonal treatment. Their prognosis depends on the precocity of the diagnosis, the location and the size of the tumor.
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