Abstract
Craniopharyngiomas are an unusual group of epithelial tumors thought to be derived from the embryonic remnants of an incompletely involuted hypophyseal-pharyngeal duct (Erdheim 1904). The name of the tumor was first introduced by Cushing in 1932, and has been considered by many to be a misnomer as Rathke’s pouch is actually an evagination of the primitive stomodeum and not the pharynx proper. They are encountered primarily in the sellar and parasellar regions but can be found anywhere along the developmental path of Rathke’s pouch (Podoshin et al. 1970). They occur with a peak incidence between 5 to 15 years of age but can present at any age (Sung et al. 1981). Visual loss and impairment, headache, apathy, depression, incontinence,hypersomnia, cognitive deficits, memory loss,sexual dysfunction, and growth failure are typical symptoms. Hydrocephalus and endocrine disorders are often present at the time of diagnosis (Carmel 1982). Due to the slow growth rate of these tumors,they are often quite large before becoming symptomatic.
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Khoo, L.T., Flagel, J., Liker, M., Levy, M.L. (2003). Craniopharyngiomas: Surgical Management. In: Petrovich, Z., Brady, L.W., Apuzzo, M.L.J., Bamberg, M. (eds) Combined Modality Therapy of Central Nervous System Tumors. Medical Radiology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-56411-6_10
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