Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/17981
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dc.contributor.authorVoulgaris, S. G.en
dc.contributor.authorPartheni, M.en
dc.contributor.authorTzortzidis, F.en
dc.contributor.authorRavazoula, P.en
dc.contributor.authorPessach, I. S.en
dc.contributor.authorPapadakis, N.en
dc.contributor.authorPolyzoidis, K. S.en
dc.date.accessioned2015-11-24T18:49:32Z-
dc.date.available2015-11-24T18:49:32Z-
dc.identifier.issn0722-5091-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/17981-
dc.rightsDefault Licence-
dc.subjectAdenoma/pathologyen
dc.subjectBrain Neoplasms/metabolism/*pathology/surgeryen
dc.subjectCraniopharyngioma/pathologyen
dc.subjectDiabetes Insipidus/etiologyen
dc.subjectDiagnosis, Differentialen
dc.subjectFatal Outcomeen
dc.subjectHeadache/etiologyen
dc.subjectHumansen
dc.subjectImmunohistochemistryen
dc.subjectMagnetic Resonance Imagingen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectNeurosurgical Procedures/adverse effectsen
dc.subjectParaganglioma/metabolism/*pathology/surgeryen
dc.subjectPituitary Neoplasms/metabolism/*pathology/surgeryen
dc.subjectVision Disorders/etiologyen
dc.titleSuprasellar and intrasellar paragangliomasen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/17007444-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate2006-
heal.abstractNeoplasms of the sellar region are entities with a large differential diagnosis. Although paraganglionic cells have not been demonstrated in the pituitary or adjacent structures, the existence of sellar region paragangliomas is well-documented. To elucidate, in this area the nature of these unusual tumors is relatively difficult. Clinical history, physical examination, radiographic investigation as well as intraoperative gross observation are the same as those of sellar meningioma or pituitary adenoma. Immunohistochemistry, using neuroendocrine markers and electron microscopy are the two definitive diagnostic methods to differentiate among these entities. The clinical management, the possible pathogenesis of the tumor, the importance of immunohistochemistry in making the diagnosis and the clinical outcome of these patients are discussed.en
heal.journalNameClin Neuropatholen
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ

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