Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/20476
Full metadata record
DC FieldValueLanguage
dc.contributor.authorKalantaridou, S. N.en
dc.contributor.authorBraddock, D. T.en
dc.contributor.authorPatronas, N. J.en
dc.contributor.authorNelson, L. M.en
dc.date.accessioned2015-11-24T19:07:53Z-
dc.date.available2015-11-24T19:07:53Z-
dc.identifier.issn0268-1161-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/20476-
dc.rightsDefault Licence-
dc.subjectAdulten
dc.subjectAutoimmune Diseases/*drug therapy/pathologyen
dc.subjectCushing Syndrome/chemically induceden
dc.subjectDexamethasone/adverse effects/therapeutic useen
dc.subjectFemaleen
dc.subjectGlucocorticoids/adverse effects/*therapeutic useen
dc.subjectHumansen
dc.subjectIatrogenic Diseaseen
dc.subjectImmunosuppressive Agents/adverse effects/*therapeutic useen
dc.subjectKneeen
dc.subjectOophoritis/drug therapy/pathology/physiopathologyen
dc.subjectOsteonecrosis/chemically induced/pathologyen
dc.subjectPrednisone/therapeutic useen
dc.subjectPrimary Ovarian Insufficiency/*drug therapy/pathology/physiopathologyen
dc.titleTreatment of autoimmune premature ovarian failureen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/10402388-
heal.identifier.secondaryhttp://humrep.oxfordjournals.org/content/14/7/1777.full.pdf-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate1999-
heal.abstractThere is no known immunosuppressive therapy for autoimmune premature ovarian failure that has been proven safe and effective by prospective randomized placebo-controlled study. Nevertheless, immunosuppression using corticosteroids has been used on an empirical basis for this condition. Here we present two cases of young women with premature ovarian failure who were treated with glucocorticoids in the hopes of restoring fertility. The first case illustrates the potential benefit of such therapy, and the second case illustrates a potential risk. The first patient with histologically proven autoimmune oophoritis was treated with alternate day glucocorticoid treatment. She had return of menstrual bleeding six times and ovulatory progesterone concentrations four times over a 16 week period. The second patient with presumed but unconfirmed autoimmune ovarian failure was referred to us after having been treated with a 9 month course of corticosteroids. During that treatment her menses did not resume. The corticosteroid treatment was complicated by iatrogenic Cushing syndrome and osteonecrosis of the knee. Identifying patients with autoimmune premature ovarian failure presents the opportunity to restore ovarian function by treating these patients with the proper immune modulation therapy. On the other hand, potent immune modulation therapy can have major complications. Corticosteroid therapy for autoimmune premature ovarian failure should be limited to use in placebo-controlled trials designed to evaluate the safety and efficacy of such treatment.en
heal.journalNameHum Reproden
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ

Files in This Item:
File Description SizeFormat 
Kalantaridou-1999-Treatment of autoimm.pdf205.13 kBAdobe PDFView/Open    Request a copy


This item is licensed under a Creative Commons License Creative Commons