Bullous Symmetric Drug-Related Intertriginous and Flexural Exanthem Secondary to Trimethoprim/Sulfamethoxazole

Symmetric drug-related intertriginous and flexural exanthem (SDRIFE) is a rare delayed-type hypersensitivity reaction that is considered a variant of systemic allergic contact dermatitis. It is typically triggered by drugs such as beta-lactam antibiotics or antihypertensives. The reaction presents as erythema with flexural prominence. However, we report a particularly rare blistering variant following administration of trimethoprim/sulfamethoxazole (TMP/SMX). Although the histopathological findings were nonspecific, the distribution and lack of systemic and mucosal involvement allowed distinction from other blistering cutaneous adverse reactions with flexural prominence. This case highlights the importance of differentiating SDRIFE from other drug eruptions with flexural distribution and includes a comprehensive differential diagnosis.

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Journal
Cureus
Published
2024-11-07
DOI
https://doi.org/10.7759/cureus.73248
Primary Topic
Drug-Induced Adverse Reactions
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article
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article

Bullous Symmetric Drug-Related Intertriginous and Flexural Exanthem Secondary to Trimethoprim/Sulfamethoxazole

Mahtab Forouzandeh, Kiran Motaparthi, Austin J. Maddy, Maheera Farsi et al.
2 links
Cureus
Drug-Induced Adverse Reactions
article

Bullous Symmetric Drug-Related Intertriginous and Flexural Exanthem Secondary to Trimethoprim/Sulfamethoxazole

Mahtab Forouzandeh, Kiran Motaparthi, Austin J. Maddy, Maheera Farsi, Asena Markal
article en

Abstract

Symmetric drug-related intertriginous and flexural exanthem (SDRIFE) is a rare delayed-type hypersensitivity reaction that is considered a variant of systemic allergic contact dermatitis. It is typically triggered by drugs such as beta-lactam antibiotics or antihypertensives. The reaction presents as erythema with flexural prominence. However, we report a particularly rare blistering variant following administration of trimethoprim/sulfamethoxazole (TMP/SMX). Although the histopathological findings were nonspecific, the distribution and lack of systemic and mucosal involvement allowed distinction from other blistering cutaneous adverse reactions with flexural prominence. This case highlights the importance of differentiating SDRIFE from other drug eruptions with flexural distribution and includes a comprehensive differential diagnosis.

CureusVol. 16(11)
Augusta University (US), University of Florida (US), Florida College (US)
Good health and well-being
Openalex Percentile: Top 80%
Drug-Induced Adverse Reactions
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