Kalir T, Friedman F
Department of Pathology, Mount Sinai School of Medicine, New York, NY 10029, USA.
Mt Sinai J Med. 1998 Sep;65(4):292-5.
Gynandroblastoma is an extremely rare tumor, composed of sex cord and stromal cells of both ovarian (granulosa-theca) and testicular (Sertoli-Leydig) types. We believe that its occurrence during pregnancy has not been previously reported. The patient was a 32-year-old woman who during her pregnancy was noted to have a progressively enlarging, unilocular left ovarian cyst. Beginning at 18 weeks gestation, the fetus required multiple platelet transfusions for severe alloimmune thrombocytopenia. A viable baby girl was delivered by cesarean section at 39 weeks gestation. At that time, an ovarian cystectomy also was performed. When the histology of the tissue subsequently became known, a left salpingo-oophorectomy was performed for gynandroblastoma. One year later, at the time of laparoscopic sterilization, the examination of the pelvis was normal.
两性母细胞瘤是一种极其罕见的肿瘤,由卵巢型(颗粒-卵泡膜细胞)和睾丸型(支持-间质细胞)的性索及间质细胞组成。我们认为其在孕期发生的情况此前尚无报道。该患者为一名32岁女性,孕期发现左侧卵巢有一个逐渐增大的单房囊肿。妊娠18周起,胎儿因严重的同种免疫性血小板减少症需要多次输注血小板。孕39周时行剖宫产娩出一名存活女婴。当时同时进行了卵巢囊肿切除术。组织学检查结果明确后,因两性母细胞瘤行左侧输卵管卵巢切除术。一年后,在腹腔镜绝育手术时,盆腔检查正常。