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妊娠12周后母体地塞米松治疗对21-羟化酶缺乏所致肾上腺生殖器综合征胎儿生殖器发育的影响

[The effect of maternal dexamethasone treatment after the 12th week of pregnancy on fetal genital development in adrenogenital syndrome with 21-hydroxylase deficiency].

作者信息

Schwab K O, Kruse K, Dörr H G, Horwitz A E, Spingler H

机构信息

Kinderklinik Universität Würzburg.

出版信息

Monatsschr Kinderheilkd. 1989 May;137(5):293-6.

PMID:2786992
Abstract

Prenatal treatment with dexamethasone starting with gestation week 5 has been proposed to prevent virilization of female fetuses with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency. We report dexamethasone treatment in a mother during her third pregnancy; this treatment could not be started before the 12th week of gestation. The second child (index case) had a simple virilizing 21-hydroxylase deficiency CAH and Prader IV genitalia. Because after amniocentesis a normal female karyotype and HLA identity with the index case were found, the dexamethasone treatment (3 x 0.5 mg/die) was continued until delivery.-In contrast to patients with salt-wasting CAH, the 17-alpha-hydroxyprogesterone level in the amniotic fluid was within the normal range. Decreased maternal plasma and urine estriol concentrations, as well as the plasma cortisol values, demonstrated adequate suppression of the fetal and maternal adrenal gland. No side effects were found in the mother as a result of the dexamethasone treatment. The newborn had virilization of the external genitalia according to Prader III but without hypertrophy of the clitoris. The degree of rugated scrotum was less marked in relation to the index case and the sinus urogenitalis was more distally shifted. Thus, surgery on the clitoris could be avoided. The conditions for further surgery (vaginoplasty) could probably be improved. Therefore, dexamethasone treatment of a mother with a female CAH fetus due to 21-hydroxylase deficiency seems to be justified starting at the 12th week of gestation. However, the optimal beginning of therapy is in early pregnancy.

摘要

有人提出从妊娠第5周开始用地塞米松进行产前治疗,以预防因21-羟化酶缺乏导致先天性肾上腺皮质增生(CAH)的女性胎儿男性化。我们报告了一位母亲在第三次怀孕期间接受地塞米松治疗的情况;该治疗在妊娠第12周之前无法开始。第二个孩子(索引病例)患有单纯男性化型21-羟化酶缺乏CAH及Prader IV型生殖器。因为羊水穿刺后发现胎儿核型正常且与索引病例HLA相同,所以地塞米松治疗(3×0.5mg/日)持续至分娩。与失盐型CAH患者不同,羊水17-α-羟孕酮水平在正常范围内。母体血浆和尿液雌三醇浓度降低以及血浆皮质醇值表明胎儿和母体肾上腺得到了充分抑制。地塞米松治疗未在母亲身上发现副作用。新生儿外生殖器有Prader III型男性化表现,但阴蒂无肥大。与索引病例相比,阴囊皱襞程度较轻,泌尿生殖窦位置更偏向远端。因此,可以避免阴蒂手术。进一步手术(阴道成形术)的条件可能会得到改善。所以,对于因21-羟化酶缺乏导致胎儿患CAH的母亲,从妊娠第12周开始用地塞米松治疗似乎是合理的。然而,最佳治疗起始时间是在妊娠早期。

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