Internal organ involvement in epidermal necrolysis and bullous fixed drug eruption assessed by 18F-fluorodeoxyglucose positron emission tomography and computed tomography: a proof-of-concept study

We investigated internal organ involvement in Stevens–Johnson syndrome (SJS), toxic epidermal necrolysis (TEN) and generalized bullous fixed drug eruption (GBFDE) using 18fluorine-fluorodeoxyglucose (18F-FDG) positron emission tomography and computed tomography (PET/CT). Participants (n = 10) underwent scans at two timepoints: acute (t0) and 3 months later (t1). Results showed increased inflammation in multiple organs at t0, with persistent or worsening inflammation in the lungs, eyes and bone marrow at t1. The study confirms internal organ involvement in SJS/TEN and GBFDE and highlights the potential of 18F-FDG PET/CT as a diagnostic tool for tracking inflammation beyond the acute stage.

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Publication Details

Journal
Clinical and Experimental Dermatology
Published
2026-02-05
DOI
https://doi.org/10.1093/ced/llag059
Primary Topic
Drug-Induced Adverse Reactions
Type
article
Field-Weighted Citation Impact
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article

Internal organ involvement in epidermal necrolysis and bullous fixed drug eruption assessed by 18F-fluorodeoxyglucose positron emission tomography and computed tomography: a proof-of-concept study

Eddy Zitha, Ashar Dhana, Lovemore Mapahla, R Lehloenya et al.
Clinical and Experimental Dermatology
Drug-Induced Adverse Reactions
article

Internal organ involvement in epidermal necrolysis and bullous fixed drug eruption assessed by 18F-fluorodeoxyglucose positron emission tomography and computed tomography: a proof-of-concept study

Eddy Zitha, Ashar Dhana, Lovemore Mapahla, R Lehloenya, Thuraya Isaacs, Tessa Kotze, Jonathan C. Peter
article en

Abstract

We investigated internal organ involvement in Stevens–Johnson syndrome (SJS), toxic epidermal necrolysis (TEN) and generalized bullous fixed drug eruption (GBFDE) using 18fluorine-fluorodeoxyglucose (18F-FDG) positron emission tomography and computed tomography (PET/CT). Participants (n = 10) underwent scans at two timepoints: acute (t0) and 3 months later (t1). Results showed increased inflammation in multiple organs at t0, with persistent or worsening inflammation in the lungs, eyes and bone marrow at t1. The study confirms internal organ involvement in SJS/TEN and GBFDE and highlights the potential of 18F-FDG PET/CT as a diagnostic tool for tracking inflammation beyond the acute stage.

Clinical and Experimental Dermatology
Western Cape Department of Health (ZA), University of Cape Town (ZA), Stellenbosch University (ZA)
Good health and well-being
Openalex Percentile: Top 63%
Drug-Induced Adverse Reactions
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