Third Department of Obstetrics and Gynecology, University of Athens, Attikon University Hospital, Athens, Greece.
Fertil Steril. 2011 Oct;96(4):1048-50. doi: 10.1016/j.fertnstert.2011.07.1103. Epub 2011 Aug 16.
To report the case of a couple with infertility and two unsuccessful previous attempts of ovarian stimulation for in vitro fertilization (IVF), whose nonclassic congenital adrenal hyperplasia (NC-CAH) due to 21-hydroxylase deficiency (21-OHD) was diagnosed and verified by molecular studies.
Case report.
Outpatient practice and academic hospital.
PATIENT(S): A woman with hyperandrogenism, luteal phase deficiency, and polycystic ovaries, and a man with oligospermia, a high rate of abnormal forms of spermatozoa (>95%), decreased sperm motility, and normal testicular volume.
INTERVENTION(S): Ultrasonography, semen analysis, endocrinologic assays, corticosteroids.
MAIN OUTCOME MEASURE(S): Increased basal and adrenocorticotropic hormone (ACTH) stimulated 17α-hydroxyprogesterone (17-OHP) values were detected in both partners. CYP21A2 genotyping revealed compound heterozygosity in both wife and husband (wife: p.P30L/p.P453S; husband: p.P453S /p.V281L).
RESULT(S): Hydrocortisone, 30 mg/day orally, was administered to both wife and husband. Forty days later, a pregnancy was detected. The prospective mother continued to receive hydrocortisone (25 mg/day) adjusted according to her hormone status. After a full-term uneventful pregnancy, a completely normal female was born. The baby had NC-CAH (genotype p.P30L/p.V281L).
CONCLUSION(S): Nonclassic congenital adrenal hyperplasia, a potential cause of infertility in couples, can be successfully treated with corticosteroids.
报道一对不孕夫妇的病例,他们曾经历过两次体外受精(IVF)卵巢刺激失败,经分子研究诊断并证实其为非经典型先天性肾上腺皮质增生症(NC-CAH),由 21-羟化酶缺乏(21-OHD)引起。
病例报告。
门诊和学术医院。
一名女性表现为高雄激素血症、黄体期不足和多囊卵巢,一名男性表现为少精子症、高比例异常形态精子(>95%)、精子活力降低和正常睾丸体积。
超声检查、精液分析、内分泌检测、皮质类固醇。
夫妇双方基础值和促肾上腺皮质激素(ACTH)刺激后 17α-羟孕酮(17-OHP)值均升高。CYP21A2 基因分型显示妻子和丈夫均为复合杂合性(妻子:p.P30L/p.P453S;丈夫:p.P453S /p.V281L)。
给予妻子和丈夫口服氢可的松,每日 30 mg。40 天后,检测到妊娠。准母亲继续根据激素状况接受调整后的氢可的松(25 mg/天)治疗。足月后顺利分娩一完全正常的女婴。该婴儿患有 NC-CAH(基因型为 p.P30L/p.V281L)。
非经典型先天性肾上腺皮质增生症是夫妇不孕的潜在原因,可以通过皮质类固醇成功治疗。