Aggressive angiomyxoma of the vagina: a case report and review of the literature

dc.contributor.authorPapachristou, D. J.en
dc.contributor.authorBatistatou, A.en
dc.contributor.authorParaskevaidis, E.en
dc.contributor.authorAgnantis, N. J.en
dc.date.accessioned2015-11-24T19:37:13Z
dc.date.available2015-11-24T19:37:13Z
dc.identifier.issn0392-2936-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/24003
dc.rightsDefault Licence-
dc.subjectBiopsy, Needleen
dc.subjectFemaleen
dc.subjectFollow-Up Studiesen
dc.subjectGynecologic Surgical Procedures/methodsen
dc.subjectHumansen
dc.subjectImmunohistochemistryen
dc.subjectMiddle Ageden
dc.subjectMyxoma/*pathology/*surgeryen
dc.subjectNeoplasm Stagingen
dc.subjectRare Diseasesen
dc.subjectRisk Assessmenten
dc.subjectTreatment Outcomeen
dc.subjectVaginal Neoplasms/*pathology/*surgeryen
dc.titleAggressive angiomyxoma of the vagina: a case report and review of the literatureen
heal.abstractAggressive angiomyxoma (AA) is a rare mesenchymal tumor of the lower pelvis and genital region, characterized by local infiltration and frequent, even multiple recurrences. In the present paper a case of a small-sized AA of the vagina, in a 55-year-old woman is reported. We describe the histological appearance and the immunohistochemical phenotype of this tumor and discuss its differential diagnosis from other mesenchymal lesions occurring in the pelvic and genital region. Furthermore, we attempt to enlighten the possible mechanisms that govern the pathogenesis and the biological behavior of this "mysterious" neoplasm.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/15285321-
heal.journalNameEur J Gynaecol Oncolen
heal.journalTypepeer-reviewed-
heal.languageen-
heal.publicationDate2004-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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