TY - JOUR ID - 697155 TI - Presentation of Dysgerminoma and Gonadoblastoma in a Patient with Swyer Syndrome JO - Journal of Obstetrics, Gynecology and Cancer Research JA - JOGCR LA - en SN - 2645-3991 AU - Hasanzadeh, Malihe AU - Rezaee, Estak AD - Obstetrics & Gynecology Department, Medicine Faculty, Mashhad University of Medical Sciences, Mashhad, Iran Y1 - 2022 PY - 2022 VL - 3 IS - 3 SP - 129 EP - 131 KW - Dysgerminoma KW - Gonadoblastoma KW - Ovary KW - Swyer Syndrome DO - 10.30699/jogcr.3.3.129 N2 - Introduction: Swyer syndrome is determined by primary amenorrhea, normal external genitalia, and the presence of a vagina, uterus, and 46XY karyotype. The aim of this case report was to introduce a patient with Swyer syndrome referred with pain and an abdominal mass. Patient Information: This case study was done in Gynecology Clinic of Ghaem Hospital in Mashhad, Iran, in 2015. A single 18-year-old woman came to the clinic with complaints of primary amenorrhea, pain, and abdominal mass underwent laparotomy. Based on her histopathology report which indicated a left ovary dysgerminoma and a right ovary gonadoblastoma, a bilateral salpingo-oophorectomy, followed by chemotherapy, was conducted. The patient was under Bleomycin, Etoposide and Platinum (BEP) chemotherapy and has been living without evidence of recurrence. Conclusion: A genetic disorder in patients younger than 20 years with an ovarian mass and diagnosis of dysgerminoma should be rejected. UR - https://www.jogcr.com/article_697155.html L1 - https://www.jogcr.com/article_697155_1efe94cdbdeeeca30085020833197181.pdf ER -