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Book

Craniopharyngioma(Archived)

In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan.
.
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Book

Craniopharyngioma(Archived)

Michael Ortiz Torres et al.
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Excerpt

Craniopharyngiomas are rare, benign tumors of the central nervous system. Craniopharyngiomas are epithelial tumors that typically arise in the suprasellar area of the brain, extending to involve the hypothalamus, optic chiasm, cranial nerves, third ventricle, and major blood vessels. It can produce a wide array of symptoms such as headaches, nausea, and vomiting, visual and endocrine disturbances. It represents a special challenge for the physicians treating it; these physicians commonly include neurosurgeons, neuro-ophthalmologists, neurologists, endocrinologists, and pediatricians. Curative surgeries are extremely difficult due to their location and infiltration into the surrounding structures. Further, the quality of life is compromised due to the development of multiple complications, including panhypopituitarism, visual problems, obesity, and mental disorders.

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Conflict of interest statement

Disclosure: Michael Ortiz Torres declares no relevant financial relationships with ineligible companies.

Disclosure: Ismat Shafiq declares no relevant financial relationships with ineligible companies.

Disclosure: Fassil Mesfin declares no relevant financial relationships with ineligible companies.

References

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    1. Feng Y, Ni M, Wang YG, Zhong LY. Comparison of neuroendocrine dysfunction in patients with adamantinomatous and papillary craniopharyngiomas. Exp Ther Med. 2019 Jan;17(1):51-56. - PMC - PubMed
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    1. Kiliç M, Can SM, Özdemir B, Tanik C. Management of Craniopharyngioma. J Craniofac Surg. 2019 Mar/Apr;30(2):e178-e183. - PubMed
    1. Müller HL, Merchant TE, Warmuth-Metz M, Martinez-Barbera JP, Puget S. Craniopharyngioma. Nat Rev Dis Primers. 2019 Nov 07;5(1):75. - PubMed

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