S5003 Risankizumab Induced Symmetrical Drug-Related Intertriginous and Flexural Exanthema (SDRIFE): An Unexpected Skin Reaction in Ulcerative Colitis Treatment

Introduction: Ulcerative colitis (UC) is a chronic, immune-mediated inflammatory bowel disease and presents with diarrhea, rectal bleeding, and urgency. It has affected over 1.5 million people in North America. Risankizumab, which is an IL-23p19 inhibitor, has recently received FDA approval in June 2024 for moderate to severe UC, based on the 2 trials INSPIRE and COMMAND, which showcased its efficacy and safety in IBD. Here we present a case of a rare cutaneous condition associated with risankizumab use. Case Description/Methods: A 56-year-old man was diagnosed with UC in 2021 and was managed with mesalamine, he eventually experienced a UC flare with pancolitis in 2023. Following this, he was switched to infliximab, which led to clinical remission. During the course, he developed palmoplantar psoriasis, which was ascribed to anti-tumor necrosis factor therapy, and infliximab was discontinued. He was started on risankizumab therapy in November 2024 and tolerated 3 induction infusions without any concerns. However, 3 days post-first subcutaneous maintenance dose in April 2025, he started developing a symmetrical erythematous rash more specific to flexural and intertriginous areas in addition to fungal infection in axillae. He received treatment with corticosteroids and antihistamines, and the rashes resolved. He received his second dose of risankizumab in May 2025, and the similar rashes recurred. He received a formal dermatological evaluation and was diagnosed with SDRIFE (Symmetrical Drug-Related Intertriginous and Flexural Exanthema) secondary to risankizumab use. We discontinued his risankizumab, and the patient received steroids and antihistamines as before. The patient was finally started on vedolizumab, and he currently remains in remission of UC both clinically and endoscopically. Discussion: The above case reveals a rare but clinically significant adverse reaction of risankizumab in UC. SDRIFE (a delayed-type hypersensitivity reaction), also known as baboon syndrome, should be considered as a possible differential diagnosis for any flexural rashes occurring after IL-23 inhibitor use. Early identification and medication discontinuation are the keys to preventing recurrence and guiding safer alternatives for IBD management.

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001147472.17532.31
Primary Topic
Psoriasis: Treatment and Pathogenesis
Type
article
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article

S5003 Risankizumab Induced Symmetrical Drug-Related Intertriginous and Flexural Exanthema (SDRIFE): An Unexpected Skin Reaction in Ulcerative Colitis Treatment

The American Journal of Gastroenterology
Psoriasis: Treatment and Pathogenesis
article

S5003 Risankizumab Induced Symmetrical Drug-Related Intertriginous and Flexural Exanthema (SDRIFE): An Unexpected Skin Reaction in Ulcerative Colitis Treatment

article en

Abstract

Introduction: Ulcerative colitis (UC) is a chronic, immune-mediated inflammatory bowel disease and presents with diarrhea, rectal bleeding, and urgency. It has affected over 1.5 million people in North America. Risankizumab, which is an IL-23p19 inhibitor, has recently received FDA approval in June 2024 for moderate to severe UC, based on the 2 trials INSPIRE and COMMAND, which showcased its efficacy and safety in IBD. Here we present a case of a rare cutaneous condition associated with risankizumab use. Case Description/Methods: A 56-year-old man was diagnosed with UC in 2021 and was managed with mesalamine, he eventually experienced a UC flare with pancolitis in 2023. Following this, he was switched to infliximab, which led to clinical remission. During the course, he developed palmoplantar psoriasis, which was ascribed to anti-tumor necrosis factor therapy, and infliximab was discontinued. He was started on risankizumab therapy in November 2024 and tolerated 3 induction infusions without any concerns. However, 3 days post-first subcutaneous maintenance dose in April 2025, he started developing a symmetrical erythematous rash more specific to flexural and intertriginous areas in addition to fungal infection in axillae. He received treatment with corticosteroids and antihistamines, and the rashes resolved. He received his second dose of risankizumab in May 2025, and the similar rashes recurred. He received a formal dermatological evaluation and was diagnosed with SDRIFE (Symmetrical Drug-Related Intertriginous and Flexural Exanthema) secondary to risankizumab use. We discontinued his risankizumab, and the patient received steroids and antihistamines as before. The patient was finally started on vedolizumab, and he currently remains in remission of UC both clinically and endoscopically. Discussion: The above case reveals a rare but clinically significant adverse reaction of risankizumab in UC. SDRIFE (a delayed-type hypersensitivity reaction), also known as baboon syndrome, should be considered as a possible differential diagnosis for any flexural rashes occurring after IL-23 inhibitor use. Early identification and medication discontinuation are the keys to preventing recurrence and guiding safer alternatives for IBD management.

The American Journal of GastroenterologyVol. 120(10S2)
Good health and well-being
Openalex Percentile: Top 38%
Psoriasis: Treatment and Pathogenesis
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S5003 Risankizumab Induced Symmetrical Drug-Related Intertriginous and Flexural Exanthema (SDRIFE): An Unexpected Skin Reaction in Ulcerative Colitis Treatment · The American Journal of Gastroenterology (2025) | TGRS Research Map | TGRS