Case Reports

A rare case of keloid combined with bullous pemphigoid

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Published: 9 October 2025
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Keloids and bullous pemphigoid (BP) are two clinically and pathophysiologically distinct dermatologic disorders – the former involves abnormal scar formation due to excess collagen deposition, while the latter is an autoimmune blistering disease. We report a case of a 67-year-old man with a 19-year history of abdominal keloids and the subsequent appearance of vesicular skin lesions. Histopathologic examination revealed both keloidal fibrosis and subepidermal blister formation. Serum testing demonstrated elevated anti-BP180 antibody levels. Initial treatment with topical and systemic agents, including neomycin, glycyrrhizin, spironolactone, and minocycline, resulted in limited improvement. Subsequently, dupilumab – a monoclonal antibody against the interleukin (IL)-4 receptor α – was introduced. After two months of dupilumab therapy, the vesicular lesions resolved, keloids stabilized, serum anti-BP180 antibody levels normalized, and the Dermatology Life Quality Index (DLQI) score decreased from 11 to 2.

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Citations

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Supporting Agencies

This study was supported by grants from the National Natural Science Foundation of China (No. 81602747).
Wenyu Wu, Department of Dermatology, Huashan Hospital, Fudan University, Shanghai

National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai; Ministry of Education Key Laboratory of Contemporary Anthropology, School of Life Sciences, and Academy for Engineering and Technology, Fudan University, Shanghai, China.

How to Cite



1.
Zhang Y, Gong Y, Shi X, Chen H, Wei Y, Wu W, et al. A rare case of keloid combined with bullous pemphigoid. Dermatol Reports [Internet]. 2025 Oct. 9 [cited 2026 May 24];. Available from: https://journals.pagepress.net/dr/article/view/10484