INDIVIDUAL ARTICLE: Cutaneous and Systemic Adverse Events Associated With Topical Corticosteroid Use: A Targeted Literature Review
November 2026 | Volume 25 | Issue 11 | 10419s4 | Copyright © November 2026
Published online September 18, 2026
Adam J. Friedman MD,a Peter Lio MD,b Lawrence F. Eichenfield MD,c Lisa Weiss MMSc,d Jaclyn Agopian MPAP,e Mark G. Lebwohl MD,f Douglas DiRuggiero DMSc,g Melissa S. Seal PhD,h Scott Snyder PharmD,h Brett Stephenson PharmD,h Robert Higham MPAS,h Alexandra K. Golant MDf
aGeorge Washington University School of Medicine and Health Sciences, Washington, DC
bMedical Dermatology Associates of Chicago, Chicago, IL
cUniversity of California San Diego-School of Medicine and Rady Children’s Hospital, San Diego, CA
dGoodman Dermatology, Canton, GA
eAmerican Skin Institute, Sherman Oaks, CA
fIcahn School of Medicine at Mount Sinai, New York, NY
gSkin Cancer and Cosmetic Dermatology Center, Rome, GA
hArcutis Biotherapeutics, Inc., Westlake Village, CA
Abstract
Background: Topical corticosteroids (TCS) have been used to treat chronic inflammatory skin conditions since initial approval in 1950, which was followed by reports of cutaneous and systemic adverse events (AEs) over the succeeding decades.
Methods: A targeted literature review was performed to identify case-report and observational-study publications from August 2015 to 2025 that reported TCS-associated adverse events (AEs).
Results: The 42 publications included identification of clinically meaningful cutaneous (69.0%) and systemic AEs, including hypothalamic-pituitary-adrenal axis suppression or adrenal insufficiency (40.5%) and Cushing syndrome (47.6%). AEs ranged from mild to severe and nonserious to serious, and reports implicated prolonged (≥12 months, 45.2%) or high-potency (69.0%) TCS use.
Conclusion: Overall, these results identified an opportunity to assess TCS access requirements and the need for additional clinician awareness and education to improve TCS prescribing practices, including monitoring of AEs and cumulative steroid exposure. Improving access to anti-inflammatory therapies that have demonstrated short- and long-term safety and efficacy in clinical trials and are not steroids for patients with chronic dermatoses should be prioritized. Often, gaining access to these alternative treatments requires step-through TCS therapy or other utilization management requirements, which unnecessarily puts patients at risk for steroid-associated AEs and delays positive treatment outcomes.
INTRODUCTION
Since the 1950s, topical corticosteroids (TCS) have been used to treat chronic inflammatory dermatoses such as atopic dermatitis, psoriasis, and seborrheic dermatitis.1 Since their introduction, evidence associating TCS with cutaneous and systemic adverse events (AEs) has accumulated, particularly related to misuse, prolonged use, high-potency formulations, and application to high-risk areas.1,2
Concern over steroid-associated AEs may manifest as steroid phobia1 and can cause hesitancy among patients and caregivers to maintain an appropriate treatment plan, thus exacerbating or prolonging symptoms.3,4 TCS side effects from use in children may be impacted by higher body surface area-to-weight ratios, relatively immature cutaneous immune environment and skin barrier, and a higher likelihood of occlusive application, each of which increases systemic exposure.2,5
MATERIALS AND METHODS
A targeted literature review was performed to identify case-report and observational-study publications reporting AEs associated with TCS use. Titles and abstracts published from August 2015 in PubMed were searched in September 2025 with search term