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               <dc:title>Case Report: Localized bullous pemphigoid induced by local triggers: a case series and a proposal for diagnostic criteria based on a literature review</dc:title>
               <dc:creator>Corbella-Bagot, Lluís</dc:creator>
               <dc:creator>Gil-Lianes, Javier</dc:creator>
               <dc:creator>Fernández-Vela, Javier</dc:creator>
               <dc:creator>Marti-Marti, Ignasi</dc:creator>
               <dc:creator>Alegre Fernandez, Marta</dc:creator>
               <dc:creator>FUERTES DE VEGA, IRENE</dc:creator>
               <dc:creator>Garbayo-Salmons, Patricia</dc:creator>
               <dc:creator>Bosch-Amate, Xavier</dc:creator>
               <dc:creator>Guilabert, Antonio</dc:creator>
               <dc:subject>Pell - Malalties</dc:subject>
               <dc:subject>Radioteràpia</dc:subject>
               <dc:subject>DISEASES::Skin and Connective Tissue Diseases::Skin Diseases::Skin Diseases, Vesiculobullous::Pemphigoid, Bullous</dc:subject>
               <dc:subject>ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Therapeutics::Radiotherapy</dc:subject>
               <dc:subject>PUBLICATION CHARACTERISTICS::Publication Formats::Journal Article::Review</dc:subject>
               <dc:subject>ENFERMEDADES::enfermedades de la piel y tejido conjuntivo::enfermedades de la piel::enfermedades cutáneas vesiculoampollosas::penfigoide ampolloso</dc:subject>
               <dc:subject>TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::terapéutica::radioterapia</dc:subject>
               <dc:subject>CARACTERÍSTICAS DE PUBLICACIONES::formatos de publicación::artículo de revista::revisión</dc:subject>
               <dc:description>Bullous pemphigoid; Radiotherapy; Case report</dc:description>
               <dc:description>Penfigoide ampolloso; Radioterapia; Reporte de un caso</dc:description>
               <dc:description>Penfigoide bullós; Radioteràpia; Informe d'un cas</dc:description>
               <dc:description>Introduction: Localized bullous pemphigoid (LBP) is an infrequent bullous pemphigoid (BP) variant restricted to a body region. According to the most compelling evidence, LBP occurs in patients with pre-existent serum antibodies against the basement membrane zone, which occasionally acquire the capacity to induce disease after the influence of different local factors acting as triggers.&#xd;
Methods: We hereby present a multicenter cohort of 7 patients with LBP developed after local triggers: radiotherapy, thermal burns, surgery, rosacea, edema and a paretic leg. In addition, we conducted a review of the literature, and we propose a set of diagnostic criteria for LBP, also based on our case series and the 2022 BP guidelines from the European Academy of Dermatology and Venereology.&#xd;
Results: During follow-up, three of the patients from our series evolved to a generalized BP, with only one requiring hospitalization. Our literature search retrieved 47 articles including a total of 108 patients with LBP, with a 63% with a potential local precipitating factor previous to their diagnosis. LBP mostly affected older females, and a subsequent generalized progression occurred in 16.7% of the cases. The most frequently involved areas were the lower limbs. Radiation therapy and surgery were responsible for the inducement of nearly 2 in 3 cases of LBP. We observed a significantly higher risk of generalization in cases where the trigger led to the developing of LBP earlier (p=0.016). Our statistical analysis did not detect any other prognosis factor for generalization when assessing direct immunofluorescence, histological and serological results, or other patient related factors.&#xd;
Conclusion: LBP should be suspected in patients with recurrent localized bullous eruptions. The presence of a trauma history in the same anatomic area is reported in most cases.</dc:description>
               <dc:date>2025-10-24T10:59:41Z</dc:date>
               <dc:date>2025-10-24T10:59:41Z</dc:date>
               <dc:date>2024-01-25T13:04:17Z</dc:date>
               <dc:date>2024-01-25T13:04:17Z</dc:date>
               <dc:date>2023-06-02</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
               <dc:identifier>http://hdl.handle.net/11351/10907</dc:identifier>
               <dc:relation>Frontiers in immunology;14</dc:relation>
               <dc:relation>https://doi.org/10.3389/fimmu.2023.1160779</dc:relation>
               <dc:rights>Attribution 4.0 International</dc:rights>
               <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Frontiers Media</dc:publisher>
               <dc:source>Scientia</dc:source>
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