A patient with Swyer sydrome presenting with gonadoblastoma and dysgerminoma
Küçük Resim Yok
Tarih
1996
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
Swyer syndrome or 46 XY gonadal dysgenesis is characterized by a female phenotype with streak gonads and normal female external genitalia and complicated by the frequent occurrence of germ cell tumors. Gonadoblastoma and dysgermi¬noma are the most frequently reported malignancies. A 15 year-old female with clitoris hypertrophy and pelvic mass was found to have a gonadoblastoma in the left ovary and dysgerminoma in the right ovary. Her karyotype was 46 XY. These two synchronous tumours, made this case rare and interesting.
Swyer syndrome or 46 XY gonadal dysgenesis is characterized by a female phenotype with streak gonads and normal female external genitalia and complicated by the frequent occurrence of germ cell tumors. Gonadoblastoma and dysgermi¬noma are the most frequently reported malignancies. A 15 year-old female with clitoris hypertrophy and pelvic mass was found to have a gonadoblastoma in the left ovary and dysgerminoma in the right ovary. Her karyotype was 46 XY. These two synchronous tumours, made this case rare and interesting.
Swyer syndrome or 46 XY gonadal dysgenesis is characterized by a female phenotype with streak gonads and normal female external genitalia and complicated by the frequent occurrence of germ cell tumors. Gonadoblastoma and dysgermi¬noma are the most frequently reported malignancies. A 15 year-old female with clitoris hypertrophy and pelvic mass was found to have a gonadoblastoma in the left ovary and dysgerminoma in the right ovary. Her karyotype was 46 XY. These two synchronous tumours, made this case rare and interesting.
Açıklama
Anahtar Kelimeler
Genel ve Dahili Tıp
Kaynak
Medical Journal of Ege University
WoS Q Değeri
Scopus Q Değeri
Cilt
6
Sayı
3-4
