Porestsky L, Levesque L, Seibel M M, Smith D, Pazianos A, Hurd J, Aretz T, Flier J
Charles A. Dana Research Institute, Beth Israel Hospital, Harvard Medical School, Boston, Massachusetts 02215.
J Reprod Med. 1988 Apr;33(4):377-81.
A 20-year-old woman presented with hyperandrogenism presumed to be due to an androgen-secreting granulosa cell tumor. In order to confirm this unusual presentation, short-term tissue culture steroidogenesis of the granulosa cell tumor and contralateral polycystic ovary was performed. Testosterone and androstenedione were produced only by the polycystic ovary, whereas the tumor was producing estradiol and progesterone. The studies of in vitro steroidogenesis prevented an incorrect interpretation of the clinical presentation.
一名20岁女性因疑似分泌雄激素的颗粒细胞瘤出现高雄激素血症。为了证实这一不寻常的表现,对颗粒细胞瘤和对侧多囊卵巢进行了短期组织培养类固醇生成研究。睾酮和雄烯二酮仅由多囊卵巢产生,而肿瘤产生雌二醇和孕酮。体外类固醇生成研究避免了对临床表现的错误解读。