Ovarian dysgerminoma with Müllerian anomaly: a case report

Obstetrics & Gynecology Science

Ha Na Kim¹  Young Nam Kim¹  Dae Hoon Jeong¹  Da Hyun Kim¹  Jung Mi Byun¹  Kyung Bok Lee¹  Moon Su Sung¹  Jin Ok Park¹  Hye Kyoung Yoon² 

[1] Department of Obstetrics and Gynecology, Busan Paik Hospital, Inje University College of Medicine, Busan, .Korea;Department of Pathology, Busan Paik Hospital, Inje University College of Medicine, Busan, .Korea;

关键词: müllerian anomaly;    uterus didelphys;    gynecologic malignancy;    dysgerminoma;   

DOI  :  10.5468/ogs.2020.63.1.98

来源: DOAJ

【 摘 要 】

Müllerian anomalies are rare deformities in women, and only a few cases concerning gynecologic malignancies arising in patients with congenital uterine malformations have been reported. Herein, we present the case of a 34-year-old woman with dysgerminoma with a Müllerian anomaly (uterus didelphys). She had secondary amenorrhea, and an ovarian mass and uterus didelphys were discovered during examination. After right salpingo-oophorectomy, the tumor was confirmed as dysgerminoma, and a chromosome study revealed a normal female karyotype (46, XX). The patient completely responded to 6 cycles of chemotherapy. To our knowledge, this is the first reported case of dysgerminoma with uterus didelphys. Although gynecologic malignancies in patients with Müllerian anomalies are very rare, clinicians should be aware of the coexistence of gynecologic malignancies and uterine malformations.

【 授权许可】

Unknown