Results 131 to 140 of about 8,269 (177)
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Otolaryngologic Clinics of North America, 2011
Craniopharyngiomas are rare epithelial tumors arising along the path of the craniopharyngeal duct; therefore, they occur in the sellar or suprasellar regions. These tumors commonly lead to neurologic, endocrinological, or visual symptoms. Radical surgery is the treatment of choice in craniopharyngiomas.
Stamm, Aldo C. +2 more
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Craniopharyngiomas are rare epithelial tumors arising along the path of the craniopharyngeal duct; therefore, they occur in the sellar or suprasellar regions. These tumors commonly lead to neurologic, endocrinological, or visual symptoms. Radical surgery is the treatment of choice in craniopharyngiomas.
Stamm, Aldo C. +2 more
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2022
Craniopharyngiomas are difficult to treat because of their dense adherence to surrounding structures and the frequent presence of cysts which obscure the anatomy. The introduction of endonasal endoscopic approaches has enabled microsurgery to be performed without mortality.
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Craniopharyngiomas are difficult to treat because of their dense adherence to surrounding structures and the frequent presence of cysts which obscure the anatomy. The introduction of endonasal endoscopic approaches has enabled microsurgery to be performed without mortality.
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Pediatric Neurosurgery, 1982
The author reviews the currently accepted concepts in the treatment of craniopharyngioma in children in the light of his personal experience and of a large number of cases reported in the literature.
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The author reviews the currently accepted concepts in the treatment of craniopharyngioma in children in the light of his personal experience and of a large number of cases reported in the literature.
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Pediatric Neurosurgery, 1982
The pathogenesis, ultrastructure, and location of craniopharyngiomas of childhood are discussed. CT scanning and contrast cisternography have added to our ability to characterize these tumors. The operative approach is dictated by the size and location of the tumor.
D G, McLone, A J, Raimondi, T P, Naidich
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The pathogenesis, ultrastructure, and location of craniopharyngiomas of childhood are discussed. CT scanning and contrast cisternography have added to our ability to characterize these tumors. The operative approach is dictated by the size and location of the tumor.
D G, McLone, A J, Raimondi, T P, Naidich
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Current Treatment Options in Neurology, 2001
Current management for craniopharyngioma, a low-grade developmental neoplasm of the sellar region, is complicated by the tumor's proximity to critical neuroanatomical structures, including the optic chiasm and hypothalamus. Recommended preoperative investigations include MRI with and without gadolinium infusion, a neuro-ophthalmologic examination and a
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Current management for craniopharyngioma, a low-grade developmental neoplasm of the sellar region, is complicated by the tumor's proximity to critical neuroanatomical structures, including the optic chiasm and hypothalamus. Recommended preoperative investigations include MRI with and without gadolinium infusion, a neuro-ophthalmologic examination and a
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Intraventricular craniopharyngioma
Neurology, 1975An unusual case of an adult with a craniopharyngioma within the third ventricle is reported. The patient complained of headaches, had a history suggestive of diabetes insipidus, and presented with a severe dementia. A brain scan revealed the suprasellar midline lesion, and a pneumoencephalogram confirmed its location within the third ventricle. Therapy
J L, Rush +3 more
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Neuroradiology, 1989
A rare case of infrasellar craniopharyngioma mainly occupying the paranasal sinuses, the infratemporal fossa and the skull base is presented. The patient had been treated by an otolaryngologist as a case of mucocele of the sphenoid and ethmoid sinuses because the biopsy specimens obtained at endonasal surgery failed to confirm the true diagnosis ...
T, Akimura +4 more
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A rare case of infrasellar craniopharyngioma mainly occupying the paranasal sinuses, the infratemporal fossa and the skull base is presented. The patient had been treated by an otolaryngologist as a case of mucocele of the sphenoid and ethmoid sinuses because the biopsy specimens obtained at endonasal surgery failed to confirm the true diagnosis ...
T, Akimura +4 more
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Clinical Neurology and Neurosurgery, 2012
Infrasellar craniopharyngioma (IC) is a rare tumor. This study aimed to investigate the clinical manifestations, treatment methods, and prognosis of IC, which invades the cranial base, nasal sinuses, nasopharynx and clivus.Eleven consecutive cases of IC who received treatment in People's Liberation Army Navy General Hospital from 1988 to 2007 were ...
Xin, Yu +5 more
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Infrasellar craniopharyngioma (IC) is a rare tumor. This study aimed to investigate the clinical manifestations, treatment methods, and prognosis of IC, which invades the cranial base, nasal sinuses, nasopharynx and clivus.Eleven consecutive cases of IC who received treatment in People's Liberation Army Navy General Hospital from 1988 to 2007 were ...
Xin, Yu +5 more
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Nasopharyngeal craniopharyngioma
The Journal of Laryngology & Otology, 1975Two cases of cranipharyngiomas which were mainly located in the nasopharynz have been reported. The cystic nature of the tumour with leakage of brownish-coloured fluid helped in arriving at the diagnosis, which was confirmed on histology. Marsupulization through a transpalatal approach seems to be the treatment of choice in such cases.
U, Prasad, N K, Kwi
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Pituitary, 2008
Ideal surgical treatment of craniopharyngiomas remains a major challenge for neurosurgeons. Craniopharyngiomas grow in the deep-seated hypothalamic area that is paramount for vegetative, emotional and endocrine function, and for maintaining worthwhile life.
Jürgen, Honegger, Marcos, Tatagiba
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Ideal surgical treatment of craniopharyngiomas remains a major challenge for neurosurgeons. Craniopharyngiomas grow in the deep-seated hypothalamic area that is paramount for vegetative, emotional and endocrine function, and for maintaining worthwhile life.
Jürgen, Honegger, Marcos, Tatagiba
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