Ovarian dysgerminoma with contralateral gonadoblastoma in a 46XY phenotypic female: Swyer syndrome
dc.contributor.author | Taneli C. | |
dc.contributor.author | Genc K. | |
dc.contributor.author | Erikci V. | |
dc.contributor.author | Balik E. | |
dc.contributor.author | Erhan Y. | |
dc.contributor.author | Ozdemir N. | |
dc.contributor.author | Veral A. | |
dc.date.accessioned | 2025-04-10T11:18:31Z | |
dc.date.available | 2025-04-10T11:18:31Z | |
dc.date.issued | 1996 | |
dc.description.abstract | A 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.uri | http://hdl.handle.net/20.500.14701/53537 | |
dc.title | Ovarian dysgerminoma with contralateral gonadoblastoma in a 46XY phenotypic female: Swyer syndrome | |
dc.type | Article |