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芳香化酶抑制剂治疗先天性肾上腺皮质增生症严重骨龄超前:病例报告

Aromatase Inhibitor as Treatment for Severely Advanced Bone Age in Congenital Adrenal Hyperplasia: A Case Report.

机构信息

Department of Paediatrics, Subdivision Endocrinology, Erasmus University Medical Centre, Rotterdam, The Netherlands,

Department of Paediatrics, Subdivision Endocrinology, Erasmus University Medical Centre, Rotterdam, The Netherlands.

出版信息

Horm Res Paediatr. 2019;92(3):209-213. doi: 10.1159/000501746. Epub 2019 Aug 7.

Abstract

INTRODUCTION

Treatment with aromatase inhibitors (AI) is a potential novel treatment in patients with congenital adrenal hyperplasia (CAH) and advanced bone age (BA), to increase near adult height (NAH). Not much is known about the efficacy of AI treatment in CAH and how AI treatment will influence the management of corticosteroid treatment.

CASE PRESENTATION

At the age of 6 years and 3 months, a boy with salt-losing CAH presented with a BA 7 years in advance. Treatment with an AI (exemestane) was initiated to decelerate bone maturation. We continued the standard dosage of corticosteroid treatment. Precocious puberty was treated with 4 years of gonadotropin-releasing hormone agonist, while AI treatment was continued until attainment of NAH. His NAH 177.7 cm (-0.8 SDS) was considerably higher than his predicted adult height of 151.3 cm (-4.6 SDS) at the start of AI treatment. The higher serum androgen levels during AI treatment did not result in short adult stature.

DISCUSSION/CONCLUSION: This report shows that AI treatment can adequately decelerate bone maturation, causing predicted adult height to increase significantly in patients of CAH with accelerated bone maturation. We suggest continuing the same corticosteroid dosage during AI treatment and accepting higher serum androgen levels.

摘要

简介

在骨龄(BA)提前进展的先天性肾上腺皮质增生症(CAH)患者中,使用芳香化酶抑制剂(AI)治疗可能是一种新的治疗方法,可以增加接近成人的身高(NAH)。目前对于 AI 治疗在 CAH 中的疗效知之甚少,以及 AI 治疗将如何影响皮质类固醇治疗的管理。

病例介绍

一名患有失盐型 CAH 的男孩,6 岁零 3 个月时,BA 提前了 7 年。开始使用 AI(依西美坦)治疗以减缓骨骼成熟。我们继续使用标准剂量的皮质类固醇治疗。对性早熟进行了 4 年的促性腺激素释放激素激动剂治疗,同时继续进行 AI 治疗,直到达到 NAH。他的 NAH 为 177.7 厘米(-0.8 SDS),明显高于开始 AI 治疗时预计的成人身高 151.3 厘米(-4.6 SDS)。在 AI 治疗期间,较高的血清雄激素水平并未导致成年身高矮小。

讨论/结论:本报告表明,AI 治疗可以充分减缓骨骼成熟,导致 CAH 患者骨龄提前进展的预测成年身高显著增加。我们建议在 AI 治疗期间继续使用相同剂量的皮质类固醇,并接受较高的血清雄激素水平。

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