Successful Treatment of Keloids and Hypertrophic Scars With Systemic and Intralesional Dupilumab

医学 杜皮鲁玛 疤痕 皮肤病科 瘢痕疙瘩 特应性皮炎 增生性瘢痕 免疫失调 免疫学 免疫系统 病理
作者
Michelle S. Min,Daniel R. Mazori,Michelle S. Lee,Joseph F. Merola,Ruth Ann Vleugels,Gabriela Cobos,Avery LaChance
出处
期刊:Journal of Drugs in Dermatology [SanovaWorks]
卷期号:22 (12): 1220-1222 被引量:1
标识
DOI:10.36849/jdd.6385
摘要

Keloids and hypertrophic scars negatively impact the quality of life for millions of people in the world. Unfortunately, though many thera-peutic approaches are used to treat scars, they are often limited in efficacy with high rates of recurrence. Lately, a better understanding of the immune dysregulation of several dermatologic conditions has led to the emergence of multiple cytokine-targeted therapies for numerous conditions. Several studies have implicated T helper 2 (Th2) immune dysregulation in the development of scars and keloids, with interleukins (IL)-4 and -13 identified as pro-fibrotic mediators. Dupilumab is an IL-4 receptor alpha antagonist that inhibits the ex-pression of both IL-4 and -13. Herein, we describe a 44-year-old woman who developed numerous disfiguring hypertrophic scars and keloids after suffering from a severe herpes zoster infection. Given the number of scars, intralesional corticosteroid injections were not feasible. Therefore, treatment with systemic dupilumab was initiated. Many scars flattened, several even developing a cigarette-paper-like texture due to rapid involution. The largest and most recalcitrant keloid was further treated with intralesional dupliumab injec-tions every 2 weeks with an even more dramatic improvement noted in 2 months. To our knowledge, this is the first report of treating multiple keloids and hypertrophic scars with both systemic and intralesional dupilumab. Dermatologists may want to consider treating keloids that cover a large area with systemic dupilumab, a therapy with an established, reassuring safety profile. The most recalcitrant areas may further benefit from concentrating dupilumab by intralesional delivery.
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