Evidence map›Paper›PMID 40552108›Full record

ArticleCase reports in pediatrics2025

Mometasone Furoate-Induced Iatrogenic Cushing's Syndrome and Secondary Adrenal Insufficiency: A Case Report.

Anna Insalaco, Sara Vandelli, Simona F Madeo, Patrizia Bruzzi, Viola Trevisani, Barbara Predieri, Laura Lucaccioni, Lorenzo Iughetti

Abstract readCase Reports
In one paragraph

Article in Case reports in pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Anna InsalacoDepartment of Medical and Surgical Sciences for Mothers, Children and Adults, Post-Graduate School of Pediatrics, University of Modena and Reggio Emilia, Modena, Italy.ORCID https://orcid.org/0009-0001-0093-2612
Sara VandelliDepartment of Medical and Surgical Sciences for Mothers, Children and Adults, Post-Graduate School of Pediatrics, University of Modena and Reggio Emilia, Modena, Italy.
Simona F MadeoDepartment of Medical and Surgical Sciences for Mothers, Children and Adults, Pediatric Unit, University of Modena and Reggio Emilia, Modena, Italy.
Patrizia BruzziDepartment of Medical and Surgical Sciences for Mothers, Children and Adults, Pediatric Unit, University of Modena and Reggio Emilia, Modena, Italy.ORCID https://orcid.org/0000-0002-3850-551X
Viola TrevisaniDepartment of Medical and Surgical Sciences for Mothers, Children and Adults, Pediatric Unit, University of Modena and Reggio Emilia, Modena, Italy.ORCID https://orcid.org/0000-0001-5224-8073
Barbara PredieriDepartment of Medical and Surgical Sciences for Mothers, Children and Adults, Pediatric Unit, University of Modena and Reggio Emilia, Modena, Italy.ORCID https://orcid.org/0000-0002-3302-6886
Laura LucaccioniDepartment of Medical and Surgical Sciences for Mothers, Children and Adults, Pediatric Unit, University of Modena and Reggio Emilia, Modena, Italy.ORCID https://orcid.org/0000-0003-0288-8990
Lorenzo IughettiDepartment of Medical and Surgical Sciences for Mothers, Children and Adults, Post-Graduate School of Pediatrics, University of Modena and Reggio Emilia, Modena, Italy.ORCID https://orcid.org/0000-0003-0370-7872

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intranasal corticosteroids (INCS) are widely used to treat allergic rhinitis and nasal obstruction. While their safety profile is generally well established, both local and systemic side effects can occur. While it is well-known that a chronic exposure to systemic glucocorticoid treatment could determine Cushing's syndrome (CS) and suppression of the hypothalamic-pituitary-adrenal (HPA) axis, there is less awareness when the administration is topical or intranasal. We report the case of an 8-year-old Caucasian girl who developed Cushingoid features following prolonged INCS treatment-initially with betamethasone and subsequently with mometasone furoate. Endocrine testing revealed undetectable baseline and after stimulation cortisol levels, suggesting a condition of adrenal insufficiency secondary to the prolonged glucocorticoid exogenous administration. Temporary hydrocortisone replacement therapy was required. Even if extremely rare, pediatricians should be aware that high-dose and long-term nasal steroid administration may cause iatrogenic CS, as well as systemic glucocorticoid treatment. Clinical features are characterized by the complications of glucocorticoid excess and by the potential life-threatening complications of adrenal insufficiency. Pediatric follow-up should be scheduled during the prolonged steroid treatment and at discontinuation, with prompt referral to a Pediatric Endocrinologist if signs and symptoms of CS (or adrenal insufficiency) are noticed.

Indexed as

adrenal insufficiencycortisolCushing's syndromehypothalamic–pituitary–adrenal axisintranasal corticosteroidsside effects

Identifiers

PMID40552108
PMCPMC12185198

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.