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A Systematic Review of Drug-associated Bullous Pemphigoid

Bullous pemphigoid is an autoimmune subepithelial disease characterised by pruritus followed by urticarial plaques and finally bullae on the skin and mucosa. Drug-associated bullous pemphigoid (DABP) is a term used to describe instances of bullous pemphigoid demonstrating clinical, histological, or...

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Autores principales: VERHEYDEN, Matthew J., BILGIC, Asli, MURRELL, Dédée F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Publication of Acta Dermato-Venereologica 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207627/
https://www.ncbi.nlm.nih.gov/pubmed/32176310
http://dx.doi.org/10.2340/00015555-3457
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author VERHEYDEN, Matthew J.
BILGIC, Asli
MURRELL, Dédée F.
author_facet VERHEYDEN, Matthew J.
BILGIC, Asli
MURRELL, Dédée F.
author_sort VERHEYDEN, Matthew J.
collection PubMed
description Bullous pemphigoid is an autoimmune subepithelial disease characterised by pruritus followed by urticarial plaques and finally bullae on the skin and mucosa. Drug-associated bullous pemphigoid (DABP) is a term used to describe instances of bullous pemphigoid demonstrating clinical, histological, or immunopathological features identical or similar to those of the idiopathic form of bullous pemphigoid, associated with the systemic ingestion, or topical application of particular drugs. In this study, we conducted a comprehensive search of the literature according to PRISMA guidelines and a total of 170 publications were included in the final qualitative analysis. In conclusion, 89 drugs were implicated in DABP. The strongest evidence for DABP is seen with gliptins, PD-1/PD-L1 inhibitors, loop diuretics, penicillin and derivatives. An appreciation of the medications associated with bullous pemphigoid enables clinicians to identify potential cases of DABP earlier and cease the offending medication.
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spelling pubmed-92076272022-10-20 A Systematic Review of Drug-associated Bullous Pemphigoid VERHEYDEN, Matthew J. BILGIC, Asli MURRELL, Dédée F. Acta Derm Venereol Systematic Review Bullous pemphigoid is an autoimmune subepithelial disease characterised by pruritus followed by urticarial plaques and finally bullae on the skin and mucosa. Drug-associated bullous pemphigoid (DABP) is a term used to describe instances of bullous pemphigoid demonstrating clinical, histological, or immunopathological features identical or similar to those of the idiopathic form of bullous pemphigoid, associated with the systemic ingestion, or topical application of particular drugs. In this study, we conducted a comprehensive search of the literature according to PRISMA guidelines and a total of 170 publications were included in the final qualitative analysis. In conclusion, 89 drugs were implicated in DABP. The strongest evidence for DABP is seen with gliptins, PD-1/PD-L1 inhibitors, loop diuretics, penicillin and derivatives. An appreciation of the medications associated with bullous pemphigoid enables clinicians to identify potential cases of DABP earlier and cease the offending medication. Society for Publication of Acta Dermato-Venereologica 2020-08-17 /pmc/articles/PMC9207627/ /pubmed/32176310 http://dx.doi.org/10.2340/00015555-3457 Text en © 2020 Acta Dermato-Venereologica https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the CC BY-NC license
spellingShingle Systematic Review
VERHEYDEN, Matthew J.
BILGIC, Asli
MURRELL, Dédée F.
A Systematic Review of Drug-associated Bullous Pemphigoid
title A Systematic Review of Drug-associated Bullous Pemphigoid
title_full A Systematic Review of Drug-associated Bullous Pemphigoid
title_fullStr A Systematic Review of Drug-associated Bullous Pemphigoid
title_full_unstemmed A Systematic Review of Drug-associated Bullous Pemphigoid
title_short A Systematic Review of Drug-associated Bullous Pemphigoid
title_sort systematic review of drug-associated bullous pemphigoid
topic Systematic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207627/
https://www.ncbi.nlm.nih.gov/pubmed/32176310
http://dx.doi.org/10.2340/00015555-3457
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