Song Eun-Seop, Lee Jung-Pil, Han Jae-Ho, Kim Ho-Yeon, Mun Se-Hee, Ryu Hee-Sug, Chang Ki-Hong
Department of Obstetrics and Gynecology, Inha University School of Medicine, Incheon, South Korea.
Gynecol Endocrinol. 2007 Jan;23(1):34-7. doi: 10.1080/09513590601095111.
Ovarian dysgerminoma is usually hormonally inert, but when it contains syncytiotrophoblastic giant cells or undergoes malignant transformation, the level of estradiol might be elevated. A 6-year-old girl contracted ovarian dysgerminoma with precocious puberty, and her levels of beta-human chorionic gondaotropin, alpha-fetoprotein and estradiol were high. After resection of the tumor, levels of tumor markers became normal and precocious puberty disappeared. We report this unusual type of dysgerminoma with a brief review of the literature.
卵巢无性细胞瘤通常无激素活性,但当它含有合体滋养层巨细胞或发生恶性转化时,雌二醇水平可能会升高。一名6岁女孩患卵巢无性细胞瘤并伴有性早熟,其β-人绒毛膜促性腺激素、甲胎蛋白和雌二醇水平均升高。肿瘤切除后,肿瘤标志物水平恢复正常,性早熟症状消失。我们报告这种不寻常类型的无性细胞瘤,并对相关文献进行简要回顾。