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妊娠期库欣综合征——甲吡酮治疗

Cushing's syndrome in pregnancy--treatment with metyrapone.

作者信息

Gormley M J, Hadden D R, Kennedy T L, Montgomery D A, Murnaghan G A, Sheridan B

出版信息

Clin Endocrinol (Oxf). 1982 Mar;16(3):283-93. doi: 10.1111/j.1365-2265.1982.tb00718.x.

Abstract

A 23-year-old female presented with severe Cushing's syndrome in the 23rd week of pregnancy. Investigations showed plasma cortisol 770 nmol/l (08.00 h) and 850 nmol/l (23.00 h); plasma ACTH was 10 ng/l (08.00 h) and 27 ng/l (23.00 h); urinary free cortisol excretion was 2460 nmol/24 h. Dexamethasone 2 mg 6-hourly for 48 h suppressed the 08.00 h plasma cortisol only to 680 nmol/l. Abdominal C.T. scan showed a right adrenal adenoma. The patient was treated with metyrapone and a good clinical improvement ensued. Plasma cortisol was reduced to 300-500 nmol/l. Depsite ultrasonographic evidence of normal fetal growth, urinary oestriol excretion was markedly deficient. Prior to the spontaneous onset of labour, there was a marked rise in plasma cortisol despite continuous metyrapone treatment. A normal female infant was born at 37 weeks' gestation. The maternal adrenal adenoma was subsequently removed. The deficiency of oestriol synthesis during the pregnancy may be explained by metyrapone-induced inhibition of C19-hydroxylation.

摘要

一名23岁女性在怀孕第23周时出现严重的库欣综合征。检查显示血浆皮质醇在上午8点时为770 nmol/l,晚上11点时为850 nmol/l;血浆促肾上腺皮质激素在上午8点时为10 ng/l,晚上11点时为27 ng/l;尿游离皮质醇排泄量为2460 nmol/24小时。每6小时服用2毫克地塞米松,持续48小时,仅将上午8点的血浆皮质醇抑制到680 nmol/l。腹部CT扫描显示右肾上腺腺瘤。患者接受甲吡酮治疗,临床症状明显改善。血浆皮质醇降至300 - 500 nmol/l。尽管超声检查显示胎儿生长正常,但尿雌三醇排泄明显不足。在自然分娩前,尽管持续使用甲吡酮治疗,血浆皮质醇仍显著升高。一名正常女婴在妊娠37周时出生。产妇的肾上腺腺瘤随后被切除。孕期雌三醇合成不足可能是由甲吡酮诱导的C19羟化抑制所解释。

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