Dermal Hypersensitivity Reaction to Semaglutide: Two Case Reports

April 2023 | Volume 22 | Issue 4 | 413 | Copyright © April 2023


Published online March 14, 2023

doi:10.36849/JDD.6550 Citation: Ouellette S, Frias G, Shah R, et al. Dermal hypersensitivity reaction to semaglutide: Two case reports. J Drugs Dermatol. 2023;22(4):413-415. doi:10.36849/JDD.6550

Samantha Ouellette BA, Giulia Frias BA, Radhika Shah MD PharmD, Mahin Alamgir MD, Cindy Wassef MD

Department of Dermatology, Rutgers Robert Wood Johnson Medical School, Somerset, NJ

Abstract
Glucagon-like peptide-1 (GLP-1) receptor agonists are a class of antidiabetic agents that work by inducing insulin secretion and inhibiting release of glucagon in a glucose-dependent manner. They are especially promising given their long duration of action, decreased risk of hypoglycemia, and added benefit of weight loss. Semaglutide is a GLP-1 receptor agonist that has been approved for type II diabetes and chronic weight management in obese adults. Cases of hypersensitivity reactions have been previously reported in patients taking GLP-1 receptor agonists dulaglutide and liraglutide. However, to our knowledge, there have been no reports of hypersensitivity reactions to semaglutide. Here, we present two cases of dermal hypersensitivity reactions in patients taking semaglutide for type II diabetes. In the first case, a 75-year-old woman who had been taking semaglutide for 10 months presented with an eruption on her legs, back, and chest for 3 months duration. Histology showed a subepidermal blister with eosinophils, suggestive of a drug hypersensitivity reaction. In the second case, a 74-year-old white man who had been taking semaglutide for 1 month presented with an eruption on the bilateral flanks and lower abdomen for 3 weeks duration. Histology revealed perivascular inflammatory cell infiltrate with eosinophils, also suggestive of a drug hypersensitivity reaction. Both patients began experiencing resolution of their symptoms within 1 month of discontinuing semaglutide.

J Drugs Dermatol. 2023;22(4): doi:10.36849/JDD.6550

Citation: Ouellette S, Frias G, Shah R, et al. Dermal hypersensitivity reaction to semaglutide: Two case reports. J Drugs Dermatol. 2023;22(4):413-415. doi:10.36849/JDD.6550

INTRODUCTION

Semaglutide is a glucagon-like peptide-1 (GLP-1) analog that was FDA-approved in 2017 for treatment of type II diabetes and in 2021 for treatment for chronic weight management in adults with obesity or overweight with at least one weight-related condition.1 Due to its longer duration of action, it is typically administered subcutaneously once weekly. The safety profile of semaglutide is similar to other GLP-1 agonists.2 The main reported adverse events associated with semaglutide were gastrointestinal including nausea, vomiting, diarrhea, abdominal pain, and constipation.2 Less than 1% of patients in an efficacy and safety trial reported a skin adverse event.2

CASE PRESENTATIONS

Case 1
A 75-year-old woman with a history of type II diabetes presented with an itchy rash on her legs, back, and chest for 3 months duration. The patient was started on semaglutide for her diabetes approximately 10 months prior to presentation. She reported using hydrocortisone cream on the lesions with minimal improvement. On physical exam, the patient had multiple 1-2 cm erythematous, scaly plaques located on the back, chest, and legs, some were excoriated with hemorrhagic crust (Figure 1). Few bullae were also present. Differential diagnosis at that time
included a drug hypersensitivity reaction, and the patient was prescribed triamcinolone 0.1% ointment to apply to the affected areas. At her 1 month follow up appointment, only minimal improvement was noted. A shave biopsy of a lesion was then taken, and histological examination showed a subepidermal blister with eosinophils. A direct immunofluorescence test was also performed that was negative. Given the findings on histology, a drug-induced dermal hypersensitivity reaction was suspected and semaglutide was discontinued. At a follow up appointment 3 weeks after discontinuing semaglutide, the patient had not experienced any new lesions and old lesions were in the process of healing.