Results 191 to 200 of about 10,682 (216)
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International Journal of Radiation Oncology*Biology*Physics, 1998
The treatment regimens at presentation and recurrence, the related morbidity, and survival rates were studied for children with craniopharyngioma who were treated at King Faisal Specialist Hospital & Research Center (KFSH&RC).From 1975 to 1996, a total of 56 children younger than 18-years-old at diagnosis underwent treatment with surgery and/or ...
Y, Khafaga +5 more
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The treatment regimens at presentation and recurrence, the related morbidity, and survival rates were studied for children with craniopharyngioma who were treated at King Faisal Specialist Hospital & Research Center (KFSH&RC).From 1975 to 1996, a total of 56 children younger than 18-years-old at diagnosis underwent treatment with surgery and/or ...
Y, Khafaga +5 more
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Controversies on Craniopharyngioma
1991The current treatment of cystic or solid craniopharingiomas are discussed. The role of microsurgical removal, external beam irradiation, stereotactic intracavitary irradiation and stereotactic radiosurgery is examinated. The ideal goal of surgical treatment is a radical removal of the lesion, avoiding the endocrinological and visual deficits.
PARLATO, Ciro +2 more
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Pituitary, 2012
One of the most challenging parasellar tumors, the craniopharyngioma was first described by Friedrich Albert von Zenker in 1857. Following improved understanding of pituitary gland physiology and development, Jakob Erdheim became the first to accurately describe the histopathological characteristics of a craniopharyngioma.
Garni, Barkhoudarian, Edward R, Laws
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One of the most challenging parasellar tumors, the craniopharyngioma was first described by Friedrich Albert von Zenker in 1857. Following improved understanding of pituitary gland physiology and development, Jakob Erdheim became the first to accurately describe the histopathological characteristics of a craniopharyngioma.
Garni, Barkhoudarian, Edward R, Laws
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Introduction Adamantinomatous craniopharyngioma (ACP) is a significant source of morbidity in the pediatric brain tumor population. It predominantly arises from the parasellar space. The tumors proximity to key vital structures often makes gross total surgical resection challenging and sometimes clinically inadvisable.
Eric, Montgomery +3 more
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Eric, Montgomery +3 more
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The management of craniopharyngioma
Clinical Radiology, 1983Twenty-six patients with proven craniopharyngioma were treated between 1954 and 1977. Total surgical removal was achieved in three patients (11.5%). Tumour recurrence was inevitable following incomplete surgical removal alone. Fifteen patients received post-operative radiotherapy following incomplete surgical removal of the tumour and eight patients ...
N, Vyramuthu, T F, Benton
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Surgical Neurology, 1985
A tumor of Rathke's cleft origin was studied, which showed some histologic features consistent with craniopharyngioma, but also had ciliated and mucin-containing cells more commonly observed in Rathke's cleft cysts. The combination of features provides further evidence that craniopharyngiomas and Rathke's cleft cysts have a common embryonic origin.
J T, Goodrich, K D, Post, P, Duffy
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A tumor of Rathke's cleft origin was studied, which showed some histologic features consistent with craniopharyngioma, but also had ciliated and mucin-containing cells more commonly observed in Rathke's cleft cysts. The combination of features provides further evidence that craniopharyngiomas and Rathke's cleft cysts have a common embryonic origin.
J T, Goodrich, K D, Post, P, Duffy
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Contemporary Biological Insights and Clinical Management of Craniopharyngioma
Endocrine Reviews, 2023John R Apps +2 more
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