医源性库欣综合征和继发性肾上腺功能不全的儿童由于局部眼皮质类固醇:一个病例报告。

IF 0.6 Q4 OPHTHALMOLOGY
Case Reports in Ophthalmology Pub Date : 2025-02-12 eCollection Date: 2025-01-01 DOI:10.1159/000543908
Joana Santos-Oliveira, Luís Torrão, Sónia Torres-Costa, Marta Silva, Ana Catarina Pedrosa, Joana Araújo, Luís Figueira, Cláudia Oliveira-Ferreira
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引用次数: 0

摘要

医源性库欣综合征(ICS)可由多种途径给药的合成糖皮质激素引起。由皮质类固醇滴眼液引起的ICS是一种特殊事件,在儿科年龄更为常见。在此,我们报告一例ICS合并继发性肾上腺功能不全(SAI),由眼部局部皮质类固醇治疗引起。病例介绍:一名11岁女孩因特发性,慢性,非高血压,非肉芽肿性双侧前葡萄膜炎被转介到我们的眼部炎症科,外用地塞米松(滴眼液,1mg /mL)治疗1年。在过去一年中,该儿童及其母亲观察到其外表逐渐发生变化,特别是注意到库欣样面部外观的发展。实验室数据显示,早晨血清促肾上腺皮质激素(ACTH)为3.6 ng/L(7.2 ~ 63.3),早晨血清皮质醇为0.20 μg/dL(6.2 ~ 19.4)。患者接受甲氨蝶呤治疗(15mg /周,口服),局部皮质类固醇治疗逐渐减少,3个月后停用。患者停用皮质类固醇眼药水9个月后,库欣样脸消失,实验室数据改善。眼科检查显示,使用甲氨蝶呤治疗后,葡萄膜炎仍处于缓解期,无新的眼内炎症发作。结论:虽然罕见,眼科医生必须意识到ICS和SAI,并优先使用最弱效的皮质类固醇在最短的持续时间。此外,临床医生应避免突然停止长期皮质类固醇治疗,因为这可能在肾上腺功能不全的情况下引发肾上腺危机。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Iatrogenic Cushing Syndrome and Secondary Adrenal Insufficiency in a Child due to Topical Ocular Corticosteroids: A Case Report.

Iatrogenic Cushing Syndrome and Secondary Adrenal Insufficiency in a Child due to Topical Ocular Corticosteroids: A Case Report.

Iatrogenic Cushing Syndrome and Secondary Adrenal Insufficiency in a Child due to Topical Ocular Corticosteroids: A Case Report.

Introduction: Iatrogenic Cushing syndrome (ICS) can be caused by synthetic glucocorticoids administered through various routes. ICS caused by corticosteroid eye drops is an exceptional event, being more frequent in pediatric age. Herein, we describe a case of ICS associated with secondary adrenal insufficiency (SAI) caused by ocular topical corticosteroid treatment.

Case presentation: An 11-year-old girl was referred to our ocular inflammation department due to idiopathic, chronic, non-hypertensive, non-granulomatous bilateral anterior uveitis, treated with topical dexamethasone (eye drops, 1 mg/mL) for 1 year. During the past year, the child and her mother observed a gradual change in her physical appearance, particularly noting the development of a cushingoid facial appearance. Laboratory data revealed morning serum adrenocorticotropic hormone (ACTH) of 3.6 ng/L (7.2-63.3) and morning serum cortisol of 0.20 μg/dL (6.2-19.4). She was treated with methotrexate (15 mg/week, orally), and the topical corticosteroid regimen was progressively tapered and discontinued after 3 months. Nine months after the patient discontinued corticosteroid eye drops, her cushingoid face disappeared, and her laboratory data improved. Regarding the ophthalmological examination, the uveitis remained in remission with methotrexate, with no new episodes of intraocular inflammation.

Conclusion: Although rare, ophthalmologists must be aware of ICS and SAI and prioritize using the least potent corticosteroid for the shortest duration necessary. Additionally, clinicians should avoid abrupt cessation of long-term corticosteroid therapy as this can precipitate an adrenal crisis in the presence of adrenal insufficiency.

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来源期刊
CiteScore
0.90
自引率
0.00%
发文量
129
审稿时长
12 weeks
期刊介绍: This peer-reviewed online-only journal publishes original case reports covering the entire spectrum of ophthalmology, including prevention, diagnosis, treatment, toxicities of therapy, supportive care, quality-of-life, and survivorship issues. The submission of negative results is strongly encouraged. The journal will also accept case reports dealing with the use of novel technologies, both in the arena of diagnosis and treatment. Supplementary material is welcomed. The intent of the journal is to provide clinicians and researchers with a tool to disseminate their personal experiences to a wider public as well as to review interesting cases encountered by colleagues all over the world. Universally used terms can be searched across the entire growing collection of case reports, further facilitating the retrieval of specific information. Following the open access principle, the entire contents can be retrieved at no charge, guaranteeing easy access to this valuable source of anecdotal information at all times.
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