Results 181 to 190 of about 10,682 (216)
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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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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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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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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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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
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Craniopharyngioma in Childhood
Advances in Pediatrics, 2006In summary, much progress has been made in our understanding of childhood craniopharyngiomas. These histologically benign but "geographically malignant" tumors are challenging to treat and require experienced clinicians from multiple disciplines including neurosurgery, radiology, hematology/oncology, ophthalmology, endocrinology, and general pediatrics
Joshua A, May +3 more
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Neurologic Clinics, 1991
Craniopharyngioma of childhood is a different entity than the tumor found in adulthood. Microscopically adamantinomata tissue is found in children whereas a squamous epithelial origin is more predominant in adults. Partial resection is of little benefit in children because adamantinomous tumors grow at a fast rate.
R A, Sanford, M S, Muhlbauer
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Craniopharyngioma of childhood is a different entity than the tumor found in adulthood. Microscopically adamantinomata tissue is found in children whereas a squamous epithelial origin is more predominant in adults. Partial resection is of little benefit in children because adamantinomous tumors grow at a fast rate.
R A, Sanford, M S, Muhlbauer
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Journal of Comparative Pathology, 1985
Craniopharyngiomas are rare in dogs. A 3 cm suprasellar craniopharyngioma in a 13-month-old male mongrel dog is described. The mass consisted of multiple microcysts and solid areas with mesenchymal proliferation in areas of transition. Tumour cells were arranged in solid sheets or separated into islands by thick bands of collagen.
K L, Hawkins, R W, Diters, J T, McGrath
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Craniopharyngiomas are rare in dogs. A 3 cm suprasellar craniopharyngioma in a 13-month-old male mongrel dog is described. The mass consisted of multiple microcysts and solid areas with mesenchymal proliferation in areas of transition. Tumour cells were arranged in solid sheets or separated into islands by thick bands of collagen.
K L, Hawkins, R W, Diters, J T, McGrath
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