与假性梅格斯综合征及功能性卵巢间质相关的卵巢无性细胞瘤:1例病例报道

来源 :世界核心医学期刊文摘(妇产科学分册) | 被引量 : 0次 | 上传用户:xueyanli122
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Background. We present the first case of an ovarian dysgerminoma complicated by pseudo- Meigs’ syndrome. Furthermore, this is the fourth reported case of ovarian dysgerminoma with functioning ovarian stroma resulting elevated androgen levels preoperatively. Case. A 25- year- old white female was referred to our department for abdominal swelling and a rapidly enlarging abdominal mass. Chest X- ray showed massive right pleural effusion. Abdominopelvic CT scan showed a left adnexal solid mass and ascites. Preoperative abnormally elevated hormone levels were as follows: free testosterone 7.7 pg/mL, androstenodione 13.6 ng/mL, and cortisol 29.4 μ g/dL. Left salpingo- oophorectomy and wedge resection of the right ovary were performed. Final histopathological investigation of the left ovary was dysgerminoma associated with stromal luteinization. Conclusion. Dysgerminoma should be considered in the differential diagnosis in a young patient with a pelvic mass, ascites, and pleural effusion and preoperative counseling should be directed accordingly. In addition, dysgerminomas may be accompanied by ovarian stromal luteinization and steroid hormone production, which occasionally result in chemical or clinical hyperandrogenism. Background. We present the first case of an ovarian dysgerminoma complicated by pseudo- Meigs’ syndrome. Furthermore, this is the fourth reported case of ovarian dysgerminoma with functioning ovarian stroma like elevated androgen levels preoperatively. Case. A 25- year- old white female was referred to our department for abdominal swelling and a rapidly enlarging abdominal mass. Chest X-ray showed massive right pleural effusion. Abdominopelvic CT scan showed a left adnexal solid mass and ascites. Preoperative abnormally elevated hormone levels were as follows: free testosterone 7.7 pg / mL, androstenodione 13.6 ng / mL, and cortisol 29.4 μ g / dL. Final histopathological investigation of the left ovary was dysgerminoma associated with stromal luteinization. Conclusion. Dysgerminoma should be considered in the differential diagnosis in a young patient with a pelvic mass, ascites, and pleural effusion and preoperative counseling should be accordingly able. In addition, dysgerminomas may be accompanied by ovarian stromal luteinization and steroid hormone production, which occasionally result in chemical or clinical hyperandrogenism.
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