Presentation of Dysgerminoma and Gonadoblastoma in a Patient with Swyer Syndrome
عنوان مقاله: Presentation of Dysgerminoma and Gonadoblastoma in a Patient with Swyer Syndrome
شناسه ملی مقاله: JR_JOGCR-3-3_007
منتشر شده در در سال 1397
شناسه ملی مقاله: JR_JOGCR-3-3_007
منتشر شده در در سال 1397
مشخصات نویسندگان مقاله:
Malihe Hasanzadeh - ۱ Obstetrics & Gynecology Department, Medicine Faculty, Mashhad University of Medical Sciences, Mashhad, Iran
Estak Rezaee
خلاصه مقاله:
Malihe Hasanzadeh - ۱ Obstetrics & Gynecology Department, Medicine Faculty, Mashhad University of Medical Sciences, Mashhad, Iran
Estak Rezaee
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.
کلمات کلیدی: Dysgerminoma, Gonadoblastoma, Ovary, Swyer Syndrome
صفحه اختصاصی مقاله و دریافت فایل کامل: https://civilica.com/doc/1138696/