Algunos niños continúan creciendo bien o experimentancrecimiento excesivo tras la extirpación de un craneo-faringioma, a pesar de tener deficiencias de. PDF | On Aug 1, , OSCAR CORREA BORQUEZ and others published Sindrome de Froehlich: Craneofaringioma. El objetivo de este artículo es presentar una revisión de la literatura a . odontoma, craneofaringioma, meloblastoma and carcinoma(1,8).

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Praetorius F, Ledesma-Montes C.

Craneofaringooma, J Shillito Jr, K. Long-term effects of conservative surgical procedures combined with radiation therapy. The syndrome of inappropiate secretion of antidiuretic hormone: Prog Exp Tumor Res, 30pp. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.

Endocr Pathol, 19pp. Two case reports of OCCT in two different ages, both in female individuals, one at 5 years old and the other at 35 years old are presented. J Neurosurg, 74pp. Growth in children with craniopharyngioma following surgery. The intraoral examination presented cortical expansion in the buccal aspect, hard at palpation, that occupied the bottom of the buccal aspect from approximately 1,5 cm.

Chromatin condensation is not associated with apoptosis. Craniopharyngioma in adults and children: Lymphocytic hypophysitis is an uncommon condition usually affecting women, particularly in the last part of pregnancy or in the postpartum period. World Health Organization Classification of Tumours.

N Engl J Med,pp. The great majority of these tumors show a diffuse growth pattern. Tumor cells are immunoreactive for the epithelial membrane antigen, vimentin, bcl-2, S, and galectin-3; they do not usually express or only focally express glial fibrillary acidic protein.


Clinically, craniopharyngiomas usually manifest with a combination of symptoms and signs of intracranial hypertension, visual alterations, hormone deficiencies, and hypothalamic dysfunction.

For this, the most helpful histochemical stain after hematoxylin—eosin HE is the reticulin technique, which helps differentiate the preserved acinar pattern of normal adenohypophysis from the disruption of the reticulin network seen craneodaringioma PAs 19 Fig.

Incidental findings on brain MRI in the general population.

WHO classification of tumours of the central nervous system, pp. J Clin Endocrinol Metab, 95pp. Endocrine, 28pp. Adenoma hipofisario asociado a Some PAs are intrinsically aggressive; the histological subtype based on hormone contents and cell structure continues to be the best predictive marker of aggressive behavior.

Astrocitoma pilocítico

Symptoms depend on localization, size, potential for growth, and age of onset. Postoperative prognosis in craniopharyngioma with respect to cardiovascular mortality, survival, and tumor recurrence.

All other tumors are very rare lesions 2 that mimic Craneofxringioma in neuroimaging studies, so that the final diagnosis should be made by the pathologist. J Clin Endocrinol Metab, 86pp. These are the so-called silent adenomas. An infant with Cushing’s disease due to an adrenocorticotropin-producing pituitary adenoma. Ccraneofaringioma Sparsely granulated GH-secreting adenomas are characteristically more chromophobic than densely granulated adenomas; E GH labeling is heterogeneous and less prominent arrow ; F immunohistochemistry with cytokeratin highlights fibrous bodies arrow.

This appears to be a direct effect of high serum cortisol levels on these pituitary cells. Management of the unresectable cystic craniopharyngioma by aspiration through an Ommaya reservoir drainage system.

Analysis of treatment results in craniopharyngioma.


New diagnostic strategy for atypical pituitary adenomas: Other approaches include intermittent aspiration by stereotactic puncture, placement of a reservoir, cystic wall sclerosis artichlo drugs, or internal radiation with radioisotopes. Se continuar a navegar, consideramos que aceita o seu uso. Adticulo metastatic to the pituitary gland: It does not have predilection for race or sex 1,2,12affecting in same proportion the maxilla and the jaw 1with more recurrence in the dented zones, and greater incidence in relation to the first molar 2,4,7.

Odontogenic calcificant cystic tumor: A report of two clinical cases

PAs are benign epithelial tumors derived from intrinsic cells of adenohypophysis. Intracavitary brachytherapy of cystic craniopharyngionmas.

Analysis of treatment results in craniopharyngioma. An immunocytochemical and ultrastructural study. Breast and lung cancer are craneofxringioma primary neoplasms most cranneofaringioma causing pituitary metastasis.

Morphologically, they consist of elongated piloid cells arranged in bundles, in a pattern that resembles a pilocytic astrocytoma however, unlike pilocytic astrocytoma, most pituicytomas lack the biphasic pattern, the characteristic Rosenthal fibers, and eosinophilic granular bodies.

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Astrocitoma pilocítico – Wikipedia, la enciclopedia libre

J Neurooncol, 54pp. J Clin Oncol, 3pp. Daniel Reyes Court Dpto. Eur Radiol, 15pp. J Pediatr, 83pp. The characterization of these craneofaringioa by electron microscopy may be of scientific interest, but does not affect the clinical management of these patients.