Abstract
Subcorneal pustular dermatosis (SPD) is a rare neutrophilic dermatosis characterized by pustules on the trunk and intertriginous areas. While oral dapsone is the first-line treatment for SPD, alternative options are necessary for patients with glucose-6-phosphate dehydrogenase deficiency, drug hypersensitivity reactions, or refractory disease. To date, no consensus exists regarding next-best agents for SPD. In this report, we present a patient with significant SPD who developed dapsone hypersensitivity syndrome and then was successfully treated with colchicine and adalimumab. We propose that colchicine should be considered as a second-line treatment for SPD and present a therapeutic algorithm for clinicians to utilize when patients are not candidates for dapsone, have side effects requiring drug discontinuation, or have refractory disease.
Original language | English (US) |
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Article number | 8140483 |
Pages (from-to) | 8140483 |
Journal | Case Reports in Dermatological Medicine |
Volume | 2024 |
DOIs | |
State | Published - 2024 |
Bibliographical note
Publisher Copyright:© 2024 Lindsey J. Wanberg et al.
PubMed: MeSH publication types
- Case Reports