Upadacitinib successfully treats Hailey-Hailey disease: a cases report and literature review
Hailey-Hailey disease (HHD) is a rare autosomal dominantly inherited skin disorder first described by brothers Howard and Hugh Hailey in 1939. This article reports a case of refractory Hailey-Hailey disease, which was treated with upadacitinib with remarkable efficacy after the unsatisfactory results of traditional treatment regimens. The patient was a 38-year-old male with a 2-year history of the disease. The rash improved significantly at 3 weeks of oral treatment with upadacitinib 15 mg/day and continued to improve at 12 weeks of follow-up without serious adverse effects. Together with the literature review, this study aims to investigate the efficacy and safety of the JAK inhibitor upadacitinib as a novel therapeutic regimen for Hailey-Hailey disease, and to provide a reference for the clinical treatment of refractory cases.
Authors
- Zhuochen Wu (ORCID: https://orcid.org/0000-0003-2957-6946)
- Xi Yang (ORCID: https://orcid.org/0000-0001-6588-4124)
- Guoqiang Zhang (ORCID: https://orcid.org/0000-0003-0771-7533)
- Qing Zhu
- Xiaoyu Xie
Institutions
- First Affiliated Hospital of Hebei Medical University (CN)
- National Center for Infectious Diseases (US)
- Hebei Science and Technology Department (CN)
Publication Details
- Journal
- Frontiers in Immunology
- Published
- 2026-01-14
- DOI
- https://doi.org/10.3389/fimmu.2025.1676459
- Primary Topic
- Genetic and rare skin diseases.
- Type
- article
- Field-Weighted Citation Impact
- 0.00