Adrenal Steroid Disorders Group, Division of Pediatric Endocrinology, Mount Sinai School of Medicine, New York, NY 10029, USA.
Best Pract Res Clin Endocrinol Metab. 2011 Dec;25(6):959-73. doi: 10.1016/j.beem.2011.08.004.
Adrenal disorders in pregnancy are relatively rare, yet can lead to significant maternal and fetal morbidity. Making a diagnosis is challenging as pregnancy may alter the manifestation of disease, many signs and symptoms associated with pregnancy are also seen in adrenal disease, and the fetal-placental unit alters the maternal endocrine metabolism and hormonal feedback mechanisms. The most common cause of Cushing's syndrome in pregnancy is an adrenal adenoma, followed by pituitary etiology, adrenal carcinoma, and other exceedingly rare causes. Medical therapy of Cushing's syndrome includes metyrapone and ketoconazole, but generally surgical treatment is more effective. Exogenous corticosteroid administration is the most common cause of adrenal insufficiency, followed by the endogenous causes of ACTH or CRH secretion. Primary adrenal insufficiency is least common. A low early morning cortisol <3 mcg/dL (83 mmol/L) in the non-stressed state and in the setting of typical clinical symptoms confirms the diagnosis. In the second and third trimester cortisol rises to levels 2-3 fold above those in the non-pregnant state, therefore a baseline level of <30 mcg/dL (823 mmol/L) warrants further evaluation. ACTH stimulated normal cortisol values have been established for each trimester. Hydrocortisone, which does not cross the placenta, is the glucocorticoid treatment of choice, and fludrocortisone is used as mineralocorticoid replacement in patients with primary disease. Congenital adrenal hyperplasia is an autosomal recessive disorder; 21-hydroxylase deficiency (21OHD) is the most common form of the disease. Non-classical 21OHD is most common, followed by the salt-wasting and simple virilizing forms. The treatment of choice for pregnant women affected with CAH is hydrocortisone, and fludrocortisones is added for those with the salt-wasting form of the disease. If the fetus is at risk for classical CAH, dexamethasone treatment can be used prenatally to prevent masculinization of the genitalia in a female infant. Because dexamethasone crosses the placenta, it should not be used to treat pregnant women with CAH if the fetus is not at risk for the disease.
妊娠期肾上腺疾病相对少见,但可导致母婴发病率显著升高。由于妊娠可能改变疾病的表现,许多与妊娠相关的体征和症状也可见于肾上腺疾病,且胎儿-胎盘单位改变了母体内分泌代谢和激素反馈机制,因此诊断具有挑战性。妊娠期库欣综合征最常见的病因是肾上腺腺瘤,其次是垂体病因、肾上腺癌和其他极为罕见的病因。库欣综合征的药物治疗包括美替拉酮和酮康唑,但一般手术治疗更有效。外源性皮质类固醇的应用是导致肾上腺皮质功能减退症最常见的原因,其次是 ACTH 或 CRH 分泌的内源性原因。原发性肾上腺皮质功能减退症最少见。在非应激状态和典型临床症状下,清晨皮质醇<3mcg/dL(83mmol/L)可确诊。在孕 2 至 3 期,皮质醇水平升高至非妊娠状态下的 2-3 倍以上,因此<30mcg/dL(823mmol/L)的基础水平需要进一步评估。已为每个孕期末确立了 ACTH 刺激的正常皮质醇值。不穿过胎盘的氢化可的松是糖皮质激素治疗的首选药物,而氟氢可的松则用于原发性疾病患者的盐皮质激素替代治疗。先天性肾上腺增生是一种常染色体隐性疾病;21-羟化酶缺乏症(21OHD)是最常见的疾病类型。非经典 21OHD 最常见,其次是失盐型和单纯男性化型。患有 CAH 的孕妇的治疗选择是给予氢化可的松,如果疾病为失盐型,则添加氟氢可的松。如果胎儿有患经典 CAH 的风险,可以在产前使用地塞米松治疗,以防止女性胎儿的生殖器出现男性化。由于地塞米松穿过胎盘,如果胎儿没有患 CAH 的风险,则不应用于治疗患有 CAH 的孕妇。