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Las lesiones paraselares son lesiones de muy baja prevalencia y pueden ser, entre otros tumores, aneurismas, quistes o granulomas. Craniopharyngiomas are often cystic tumors, usually suprasellar, resulting from embryonic cell remnants of Rathke’s pouch.

Although benign, these tumors can be aggressive craneofarinfioma frequently have neurological and endocrinological sequelae. Craniopharyngiomas usually develop in children or in the elderly. Symptoms depend on localization, size, potential for growth, and age of onset. Clinically, craniopharyngiomas usually manifest with a combination of symptoms and signs of intracranial hypertension, visual alterations, hormone deficiencies, and hypothalamic dysfunction.

Intracellular lesions can mimic pituitary adenoma. Neuroimaging techniques, especially magnetic resonance cranefoaringioma, allow these lesions to be characterized. Their appearance varies depending on the proportion of solid and cystic components, on the possible calcifications, and on the composition of an eventual cyst. Complete endocrinological and ophthalmological evaluation should be performed before establishing the therapeutic approach. The therapeutic options include surgery, radiotherapy, and a combination of both.

The optimal extension of surgery is controversial. Currently, a conservative approach combining less aggressive surgery with radiotherapy is preferred. Radiotherapy without surgery is only applicable in patients with very small tumors. Other approaches include intermittent aspiration by stereotactic puncture, placement of a reservoir, cystic wall sclerosis through drugs, or internal radiation with radioisotopes.


Parasellar lesions have a very low prevalence and can consist of cystic aneurysms or granulomas, among other tumors. Neuroimaging techniques, both computed tomography and MRI, are useful for characterizing the lesion.

Documentos de los Grupos de Trabajo. Clinical practice guideline for the diagnosis and treatment of craniopharyngioma and other parasellar lesions. Hospital Universitari de Bellvitge. Other approaches include intermittent aspiration by stereotactic puncture, placement of a reservoir, cystic wall sclerosis through drugs, or internal radiation with radioisotopes.

Neuroimaging techniques, both computed tomography and MRI, are useful for characterizing the lesion. crsneofaringioma

A clinical and pathological review. Cancer, 37pp. The descriptive epidemiology of craniopharyngioma. J Neurosurg, 89pp.

craneofaringioma infantil pdf reader

J Pediatr, 83pp. Correlation of clinical and pathological features in surgically treated craniopharyngiomas. J Neurosurg, 73pp. MR differentiation of adamantinous and squamous-papillary craniopharyngiomas. Am J Neuroradiol, 18pp. Am J Neuroradiol, 17pp. Endocr Pathol, 15pp. Craniopharyngiomas in children and adults: Clinical Endocrinol Oxf62pp.

Clinical features and management craniopharyngiomain adults. J Clin Endocrinol Metab, 81pp. The clinical, metabolic and endocrine features and the quality of life in craneofaringilma with childhood- onset craniopharyngioma compared with adult-onsetcraniopharyngioma.

Eur J Endocrinol,pp. Hypothalamic-pituitary dysfunction in patients with craniopharyngioma. Clin Endocrinol Oxf42pp.

Craniopharyngioma in adults and children: J Neurosurg, 97pp. The syndrome of inappropiate secretion of antidiuretic hormone: An unusual presentation for childhood craniopharyngioma: Report of three cases. Neurosurgery, 42pp. Factors affecting intellectual outcome in pediatric brain tumour patients.

Neurosurgery, 21pp. Neurobehavioral outcome in pediatric craniopharyngioma. Pediatr Neursurg, 26pp. Acta Paediatr Suppl,pp. Craniopharyngioma identification by CT and MR imaging at 1. Acta Radiol, 36pp. Am J Neuroradiol, 26pp. Cystic lesions of the pituitary: J Clin Endocrinol Metab, 84pp. Postoperative prognosis in craniopharyngioma with respect to cardiovascular mortality, survival, and tumor recurrence.


J Clin Endocrinol Metab, 83pp.

craneofaringioma infantil pdf reader – PDF Files

Surgical treatment of craniopharyngiomas: Neurosurgery, 36pp. Hypoglycemia insulin test in the assessment of the hypothalamic-pituitary-adrenal function.

Med Clin Barc, pp. Growth hormone release after glucagon as a reliable test of growth hormone assessment in adults. Clin Endocrinol Oxf56pp. Surgery with or without radiation therapy in the management of craniopharyngiomas in children and young adults. Radiology,pp. Welch, J Shillito Jr, K.

Long-term effects of conservative surgical procedures combined with radiation therapy. Analysis of treatment results in craniopharyngioma.

J Clin Oncol, 3pp. Management of the unresectable cystic craniopharyngioma by aspiration through an Ommaya reservoir drainage system. J Neurosurg, 52pp. Neurosurgery, 40 crraneofaringioma, pp. Phosphorus intracavitary irradiation of cystic craniopharyngiomas: Surgical, radiological and ophthalmological aspects.

Acta Neurochir Wien99pp. Van den Berge, G. Intracavitary brachytherapy of cystic craniopharyngionmas. J Neurosurg, 77pp. J Neurosurg, 83pp. Jude Children’s Research Hospital experience Clinical outcome in children with recurrent craniopharyngioma after primary surgery.

Cancer J, 6pp. Endocr Rev, 27pp. Eur Radiol, 15pp. Neurol Med Chir, 43pp. Adenoma hipofisario asociado a Si continua navegando, consideramos que acepta su uso. To improve our services and products, we use “cookies” own or third parties authorized to craneofarihgioma advertising related to client preferences through the analyses of navigation customer behavior.

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