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dc.contributor.authorAdal, E
dc.contributor.authorIlvan, S
dc.contributor.authorYoruk, A
dc.contributor.authorArslanoglu, I
dc.contributor.authorYildiz, M
dc.contributor.authorIsguven, P
dc.date.accessioned2021-03-03T08:39:32Z
dc.date.available2021-03-03T08:39:32Z
dc.date.issued2003
dc.identifier.citationIsguven P., Yoruk A., Adal E., Arslanoglu I., Ilvan S., Yildiz M., "Adult type granulosa cell tumor causing precocious pseudopuberty in a 6 year-old girl", JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, cilt.16, sa.4, ss.571-573, 2003
dc.identifier.issn0334-018X
dc.identifier.otherav_18b2f080-a689-4d34-8ea6-9b9bda3f685d
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/21930
dc.identifier.urihttps://doi.org/10.1515/jpem.2003.16.4.571
dc.description.abstractMalignant ovarian tumors are responsible for 2-3% of all cases of precocious pseudo-puberty (PP) in girls. The most common forms of ovarian tumors presenting as PP are the granulosa cell tumors (GCT). The clinical and pathological features of granulosa cell tumors that occur frequently in young girls, so-called juvenile granulosa cell tumors (JGCT), differ histologically from those occurring in adults. As a cause of PP in young girls, adult type granulosa cell tumors (AGCT) are extremely rare. We report a 6 year-old girl presenting with early breast development and vaginal bleeding due to a well encapsulated ovarian tumor. Microscopic features of the resected tumor were characteristic of AGCT.
dc.language.isoeng
dc.subjectİç Hastalıkları
dc.subjectEndokrinoloji ve Metabolizma Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectENDOKRİNOLOJİ VE METABOLİZMA
dc.titleAdult type granulosa cell tumor causing precocious pseudopuberty in a 6 year-old girl
dc.typeMakale
dc.relation.journalJOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
dc.contributor.department, ,
dc.identifier.volume16
dc.identifier.issue4
dc.identifier.startpage571
dc.identifier.endpage573
dc.contributor.firstauthorID168109


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