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孕期先天性肾上腺皮质增生症:处理方法取决于“患者”是谁。

Congenital adrenal hyperplasia in pregnancy: approach depends on who is the 'patient'.

作者信息

Keely Erin, Malcolm Janine

机构信息

Departments of Medicine and Obstetrics/Gynecology, University of Ottawa, Ottawa ON, Canada.

出版信息

Obstet Med. 2012 Dec;5(4):154-160. doi: 10.1258/om.2012.120015. Epub 2012 Sep 24.

Abstract

Congenital adrenal hyperplasia (CAH) is a group of autosomal-recessive disorders caused by a reduced or absent enzymatic activity at one of the stages of adrenal steroid biosynthesis. Prenatal exposure to androgens leads to external genital masculinization of the affected female child. In pregnancy, the provider may be optimizing care for the woman with CAH or targeting treatment to reduce virilization in the affected unborn child. For the affected adult woman the goals of therapy in pregnancy are to prevent adrenal insufficiency, reduce fetal exposure to androgens and glucocorticoids and to avoid damage to reconstructed genitalia. For prenatal therapy for prevention of virilization of possibly affected female children, dexamethasone is used. However, questions remain about the efficacy and safety of exposing 7/8 unaffected children in the first trimester. Prenatal treatment should only be undertaken after careful discussion with the parents of the risks and benefits in an experienced centre or as part of a research protocol.

摘要

先天性肾上腺皮质增生症(CAH)是一组常染色体隐性疾病,由肾上腺类固醇生物合成某一阶段酶活性降低或缺乏所致。产前暴露于雄激素会导致患病女童外生殖器男性化。在孕期,医疗服务提供者可能会优化对患有CAH的女性的护理,或采取针对性治疗以减少患病胎儿的男性化。对于成年患病女性,孕期治疗的目标是预防肾上腺功能不全,减少胎儿暴露于雄激素和糖皮质激素,并避免对重建的生殖器造成损伤。为预防可能患病的女童男性化而进行产前治疗时,使用地塞米松。然而,关于在孕早期让7/8未患病胎儿暴露于此治疗的有效性和安全性仍存在疑问。产前治疗应仅在经验丰富的中心与父母仔细讨论风险和益处后进行,或作为研究方案的一部分开展。

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本文引用的文献

1
Steroid 21 hydroxylase deficiency congenital adrenal hyperplasia.先天性肾上腺皮质增生症 21 羟化酶缺乏症。
Pediatr Clin North Am. 2011 Oct;58(5):1281-300, xii. doi: 10.1016/j.pcl.2011.07.012.
2
Congenital adrenal hyperplasia.先天性肾上腺增生症
J Pediatr Adolesc Gynecol. 2011 Jun;24(3):116-26. doi: 10.1016/j.jpag.2010.10.001.
4
Non-invasive prenatal diagnosis.
Methods Mol Biol. 2011;688:155-72. doi: 10.1007/978-1-60761-947-5_11.

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