<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-13T01:17:29Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:11351/11015" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:11351/11015</identifier><datestamp>2025-10-24T11:00:14Z</datestamp><setSpec>com_2072_451665</setSpec><setSpec>com_2072_378040</setSpec><setSpec>col_2072_451666</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Efectos adversos cutáneos inmunomediados por los anti-TNF: revisión de 30 casos</dc:title>
   <dc:title>Immune-Mediated Skin Reactions to Tumor Necrosis α Inhibitors: A Review of 30 Cases</dc:title>
   <dc:creator>Sin-Soler, Maria</dc:creator>
   <dc:creator>Gamissans, Marta</dc:creator>
   <dc:creator>Lara, A</dc:creator>
   <dc:creator>Ribera, M</dc:creator>
   <dc:creator>Romaní, Jorge</dc:creator>
   <dc:creator>Riera-Martí, Núria</dc:creator>
   <dc:subject>Pell - Necrosi</dc:subject>
   <dc:subject>Psoriasi</dc:subject>
   <dc:subject>Medicaments dermatològics</dc:subject>
   <dc:subject>CHEMICALS AND DRUGS::Amino Acids, Peptides, and Proteins::Peptides::Intercellular Signaling Peptides and Proteins::Cytokines::Tumor Necrosis Factors</dc:subject>
   <dc:subject>CHEMICALS AND DRUGS::Chemical Actions and Uses::Pharmacologic Actions::Physiological Effects of Drugs::Immunologic Factors</dc:subject>
   <dc:subject>DISEASES::Skin and Connective Tissue Diseases::Skin Diseases::Skin Diseases, Papulosquamous::Psoriasis</dc:subject>
   <dc:subject>COMPUESTOS QUÍMICOS Y DROGAS::aminoácidos, péptidos y proteínas::péptidos::péptidos y proteínas de señalización intercelular::citocinas::factores de necrosis tumoral</dc:subject>
   <dc:subject>ENFERMEDADES::enfermedades de la piel y tejido conjuntivo::enfermedades de la piel::enfermedades cutáneas papuloescamosas::psoriasis</dc:subject>
   <dc:subject>COMPUESTOS QUÍMICOS Y DROGAS::acciones y usos químicos::acciones farmacológicas::efectos fisiológicos de los fármacos::factores inmunitarios</dc:subject>
   <dcterms:abstract>Tumor necrosis; Inhibitor therapy; Paradoxical reaction</dcterms:abstract>
   <dcterms:abstract>Necrosis tumoral; Tratamiento con inhibidores; Reacción paradójica</dcterms:abstract>
   <dcterms:abstract>Necrosi tumoral; Tractament amb inhibidors; Reacció paradoxal</dcterms:abstract>
   <dcterms:abstract>Background: Tumor necrosis factor α (TNF) inhibitors are used to treat different inflammatory diseases. Although these biologics have an adequate safety profile, they have been associated with paradoxical reactions. &#xd;
Material and methods: Retrospective review of patients on TNF inhibitor therapy who developed a paradoxical skin reaction and were seen at the dermatology department of Hospital Universitari Parc Taulí in Sabadell, Spain.&#xd;
Results: We collected data on 30 patients under treatment with a TNF inhibitor who developed an immune-mediated skin reaction in the form of psoriasis (90%), alopecia (6.7%), or neutrophilic dermatitis (3.3%). The most common drugs involved were adalimumab (56.7%) and infliximab (40%). Psoriasiform reactions mostly manifested as generalized plaques (62.9%) or palmoplantar pustulosis (37%). Thirteen patients (43.3%) continued on the same TNF inhibitor and 12 of them (92.3%) achieved partial or complete resolution of lesions. Five patients were switched to a different TNF inhibitor, but none of them achieved complete resolution. Eight patients were switched to a biologic with a different target, and 5 of them (62.5%) achieved partial or complete resolution.&#xd;
Conclusions: Paradoxical reactions during TNF inhibitor therapy do not always require a change of treatment. In our series, the addition of a topical and/or systemic treatment resolved the skin lesions in more than half of the patients, and switching to a drug with a different target was more effective. A change of strategy should be contemplated in more serious cases.</dcterms:abstract>
   <dcterms:dateAccepted>2025-10-24T11:00:14Z</dcterms:dateAccepted>
   <dcterms:available>2025-10-24T11:00:14Z</dcterms:available>
   <dcterms:created>2025-10-24T11:00:14Z</dcterms:created>
   <dcterms:issued>2024-02-09T11:57:09Z</dcterms:issued>
   <dcterms:issued>2024-02-09T11:57:09Z</dcterms:issued>
   <dcterms:issued>2024-01</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>http://hdl.handle.net/11351/11015</dc:identifier>
   <dc:relation>Actas Dermo-Sifiliográficas;115(1)</dc:relation>
   <dc:relation>https://doi.org/10.1016/j.ad.2023.06.016</dc:relation>
   <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>Elsevier</dc:publisher>
   <dc:source>Scientia</dc:source>
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