Dupilumab treatment for pruritus-associated cutaneous sarcoidosis

Sarcoidosis is a chronic multisystemic, inflammatory disease characterized by the formation of noncaseating granulomas, with cutaneous involvement in a fraction of patients. Although existing literature reports dupilumab to cause sarcoidosis-like reactions, we present a 57-year-old man with erythrodermic sarcoidosis and atopic dermatitis refractory to numerous systemic medications that later improved with dupilumab. The improvement of his pruritus and cutaneous lesions after dupilumab initiation, followed by worsening after temporary discontinuation, then re-improvement after re-initiation supported dupilumab's therapeutic role. IL-4 and IL-13 stimulate tissue fibrosis and irreversible tissue damage in sarcoidosis, perhaps explaining dupilumab's therapeutic mechanism in this patient's case. For patients with severe sarcoidosis refractory to numerous medications, clinicians should keep in mind dupilumab as a potential option, particularly for those patients with concomitant atopic dermatitis.

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Publication Details

Journal
Dermatology Online Journal
Published
2025-09-08
DOI
https://doi.org/10.25251/btwtbw27
Primary Topic
Drug-Induced Adverse Reactions
Type
article
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article

Dupilumab treatment for pruritus-associated cutaneous sarcoidosis

Henry W. Lim, Karan Pandher, David X. Gao, Soo In Choi
Dermatology Online Journal
Drug-Induced Adverse Reactions
article

Dupilumab treatment for pruritus-associated cutaneous sarcoidosis

Henry W. Lim, Karan Pandher, David X. Gao, Soo In Choi
article en

Abstract

Sarcoidosis is a chronic multisystemic, inflammatory disease characterized by the formation of noncaseating granulomas, with cutaneous involvement in a fraction of patients. Although existing literature reports dupilumab to cause sarcoidosis-like reactions, we present a 57-year-old man with erythrodermic sarcoidosis and atopic dermatitis refractory to numerous systemic medications that later improved with dupilumab. The improvement of his pruritus and cutaneous lesions after dupilumab initiation, followed by worsening after temporary discontinuation, then re-improvement after re-initiation supported dupilumab's therapeutic role. IL-4 and IL-13 stimulate tissue fibrosis and irreversible tissue damage in sarcoidosis, perhaps explaining dupilumab's therapeutic mechanism in this patient's case. For patients with severe sarcoidosis refractory to numerous medications, clinicians should keep in mind dupilumab as a potential option, particularly for those patients with concomitant atopic dermatitis.

Dermatology Online JournalVol. 31(4)
Grand Rapids Community College (US), Henry Ford Health System (US), Michigan State University (US)
Openalex Percentile: Top 66%
Drug-Induced Adverse Reactions
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