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13 June 2025 : Case report  USA

Accelerated Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) Syndrome in Response to TMP-SMX: A Case Report

Unusual clinical course, Challenging differential diagnosis, Unusual or unexpected effect of treatment, Diagnostic / therapeutic accidents, Rare disease, Adverse events of drug therapy, Clinical situation which can not be reproduced for ethical reasons

Emily J. Sanchez ABCDEF 1*, Elizabeth A. Cheiky ABCDF 1

DOI: 10.12659/AJCR.948217

Am J Case Rep 2025; 26:e948217

Table 3 Compares and contrasts skin involvement, onset, symptoms, and mortality of Stevens-Johnson syndrome (SJS), fixed-drug eruption (FDE), and drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome.

FeatureSJSFDEDRESS
DefinitionA severe mucocutenaous reaction; characterized by widespread skin detachment and mucous membrane involvementLocalized, immune-mediated hypersensitivity reaction.Recurrent, sharply demarcated skin lesions that reappear at the same site upon subsequent exposure to offending drugSevere drug-induced hypersensitivity reaction characterized by rash, fever, hematologic abnormalities (eosinophilia), and internal organ involvement
Skin Involvement
Onset
SymptomsFlu-like symptoms, painful red or purplish skinBlisters, erosions, especially in mucosal regions (eyes, mouth, genitals)Erythematous, edematous plaques that may blister.Pruritic, painful, or asymptomatic.Post-inflammatory hyperpigmentation after resolution of acute phaseFever, rash, eosinophilia, lymphadenopathy, and multi-organ involvement (eg, liver, kidneys, lungs)
Mortality
This table was created using reference material sourced in the reference list. It is not meant to be the sole resource used in clinical practice, but instead a means of providing a single location to compare the 3 different clinical conditions. Adapted from: [].

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American Journal of Case Reports eISSN: 1941-5923
American Journal of Case Reports eISSN: 1941-5923