Keyser, Johanna

[["dc.bibliographiccitation.firstpage","107"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Gynecological Endocrinology"],["dc.bibliographiccitation.lastpage","109"],["dc.bibliographiccitation.volume","27"],["dc.contributor.author","Boettcher, Bettina"],["dc.contributor.author","Hinney, Bernd"],["dc.contributor.author","Keyser, Johanna"],["dc.contributor.author","Kuehnle, Ingrid"],["dc.contributor.author","Schweyer, Stefan"],["dc.contributor.author","Emons, Guenter"],["dc.date.accessioned","2018-11-07T08:59:28Z"],["dc.date.available","2018-11-07T08:59:28Z"],["dc.date.issued","2011"],["dc.description.abstract","Sertoli-Leydig cell tumours account for less than 0.2% of ovarian malignancies. We describe the case of a Sertoli-Leydig cell tumour in a 13-year-old girl who presented with symptoms of hyperandrogenism. We give an overview over current literature and discuss options of therapy of rare Sertoli-Leydig cell tumours.