Results 141 to 150 of about 8,269 (177)
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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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2006
The craniopharyngioma is one of the most common destructive lesions of the hypothalamus and pituitary gland. It still remains one of the most difficult tumors to treat effectively since complete resection is often impossible and is associated with frequent recurrence. Current therapy is multimodal and focuses on a combination of surgical decompression,
Rod J, Oskouian +2 more
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The craniopharyngioma is one of the most common destructive lesions of the hypothalamus and pituitary gland. It still remains one of the most difficult tumors to treat effectively since complete resection is often impossible and is associated with frequent recurrence. Current therapy is multimodal and focuses on a combination of surgical decompression,
Rod J, Oskouian +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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Surgical Neurology, 1984
A case of infrasellar craniopharyngioma is reported. This must be the first report that presents computed tomographic findings of an infrasellar craniopharyngioma. A computed tomography scan demonstrated the characteristic features of a tumor at the base of the skull extending massively into the nasopharynx, prepontine cistern, and suprasellar region ...
K, Mukada +4 more
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A case of infrasellar craniopharyngioma is reported. This must be the first report that presents computed tomographic findings of an infrasellar craniopharyngioma. A computed tomography scan demonstrated the characteristic features of a tumor at the base of the skull extending massively into the nasopharynx, prepontine cistern, and suprasellar region ...
K, Mukada +4 more
openaire +2 more sources
Child's Nervous System, 2019
Craniopharyngioma has historically been recognized to be a formidable pathology primarily due to its proximity to critical neurovascular structures and the challenging surgical corridors that surgeons have tried to reach this lesion.In this work, we review the medical and surgical management of these tumors with a focus on clinical presentation ...
Annie, Drapeau +7 more
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Craniopharyngioma has historically been recognized to be a formidable pathology primarily due to its proximity to critical neurovascular structures and the challenging surgical corridors that surgeons have tried to reach this lesion.In this work, we review the medical and surgical management of these tumors with a focus on clinical presentation ...
Annie, Drapeau +7 more
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Craniopharyngiomas in Children
Neurosurgery, 1982Abstract Forty-three children with craniopharyngiomas were operated upon at The Neurological Institute of New York between 1952 and 1977. The removal was thought to be total in 14 children and subtotal in 20, and cyst aspiration/biopsy was performed in 9 cases.
P W, Carmel, J L, Antunes, C H, Chang
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Contemporary Biological Insights and Clinical Management of Craniopharyngioma
Endocrine Reviews, 2023John Richard Apps +1 more
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