Ovarian dysgerminoma with contralateral gonadoblastoma in a 46XY phenotypic female: Swyer syndrome

Simple item page
dc.contributor.authorTaneli C.
dc.contributor.authorGenc K.
dc.contributor.authorErikci V.
dc.contributor.authorBalik E.
dc.contributor.authorErhan Y.
dc.contributor.authorOzdemir N.
dc.contributor.authorVeral A.
dc.date.accessioned2024-07-22T08:25:58Z
dc.date.available2024-07-22T08:25:58Z
dc.date.issued1996
dc.description.abstractA 15-year-old girl was admitted to the pediatric surgery department with primary amenorrhea and right inguinal swelling of one year duration. On physical examination, the patient presented with a female phenotype, but no breast development; somewhat hirsute with hypertrophic clitoris. Ultrasound examination disclosed a palpable mass originating from the right ovary. At operation, a right salpingo-ooferectomy was performed, and a biopsy specimen was obtained from the left ovary which did not appear normal. Histopathologic examination revealed a right ovarian disgerminoma and a left gonadoblastoma. One month after the first operation, a left gonadectomy was performed with accompanying cliteroplasty. An original case of Swyer syndrome is reported in a patient with female phenotype, dysgerminoma of the right and gonadoblastoma of the the left ovaries.
dc.identifier.issn10165142
dc.identifier.urihttp://akademikarsiv.cbu.edu.tr:4000/handle/123456789/20674
dc.language.isoEnglish
dc.subjectadolescent
dc.subjectarticle
dc.subjectcase report
dc.subjectdysgerminoma
dc.subjectfemale
dc.subjectgonadal dysgenesis
dc.subjectgonadectomy
dc.subjectgonadoblastoma
dc.subjecthistopathology
dc.subjecthuman
dc.titleOvarian dysgerminoma with contralateral gonadoblastoma in a 46XY phenotypic female: Swyer syndrome
dc.typeArticle

Files

Collections

Scopus Koleksiyonu