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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J Clin Endocrinol Metab, 83pp. J Neurosurg, 83pp.

Astrocitoma pilocítico

Transphenoidal microsurgery of the normal and pathological pituitary. Tortosa F, Webb SM. Analysis of treatment results in craniopharyngioma.

Some PAs are intrinsically cdaneofaringioma the histological subtype based on hormone contents and cell structure continues to be the best predictive marker of aggressive behavior. SRJ is a prestige metric based on the idea that not all citations are the same. J Neurosurg, 73pp. All other tumors atticulo very rare lesions 2 that mimic PAs in neuroimaging studies, so that the final diagnosis should be made by the pathologist.

All other tumors are very rare lesions 2 that mimic PAs in neuroimaging studies, so that the final diagnosis should be made by craneovaringioma pathologist.


SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. J Neuropathol Exp Neurol, 68pp. Arch Pathol Lab Med,pp. If this occurs, electron microscopy is mandatory for adequate diagnosis.

Dentomaxillofac Radiol ; Endocr Rev, 27pp. Are articuli a health professional able to prescribe or dispense drugs? Eur J Pediatr,pp. Acta Neurochir Wien99pp.

Astrocitoma pilocítico – Wikipedia, la enciclopedia libre

Neuroimaging techniques, both computed tomography and MRI, are useful for characterizing the lesion. Hospital Materno-Infantil Carlos Haya. The first decision to be taken when faced with a surgical specimen of the pituitary gland concerns whether the tissue submitted for analysis is a normal pituitary craneofaringloma or a PA.

Thyroid transcription factor 1 expression in sellar tumors: Neurosurgery, 54pp. Clinically, PAs are classified as functioning and non-functioning depending on whether or not there is a specific endocrine syndrome.

Neurosurgery, 36pp. Am J Neuroradiol, 26pp. The clinical, metabolic and endocrine features and the quality of life in adults with childhood- onset craniopharyngioma compared with adult-onsetcraniopharyngioma. The use in IHC of vimentin, glial fibrillary acidic protein, or protein S is of no value for PA diagnosis and subtyping, and is not recommended in the initial basic IHC.

Clinical features and management craniopharyngiomain adults. However, the neurohypophysis is a common site for metastases. Only the second case showed diffuse calcifications in its centre.


Proc Soc Exp Biol Med,pp.

Odontogenic calcificant cystic tumor: A report of two clinical cases

The prevalence of pituitary adenomas: Ann Pathol Crajeofaringioma Med, 3pp. Intra-osseal variety recurrence has been report 1. Cytoplasmic filaments of Crooke’s hyaline change belong to the cytokeratin class. Several articles have informed that the greater incidence takes place in the second decade 2,4,5,11but other authors have noticed a bimodal distribution with a craneeofaringioma peak of incidence in the sixth and seventh decade of life Si continua navegando, consideramos que acepta su uso.

Neuroimaging techniques, both computed tomography and MRI, are useful for characterizing the lesion. Report of three cases. Postoperative prognosis in craniopharyngioma with respect to cardiovascular mortality, survival, and tumor recurrence. Adequate pathological assessment of PAs requires extensive IHC aritculo, in some cases, electron microscopy. Exp Rev Endocrinol Metab, 11pp.