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Case Report: Localized bullous pemphigoid induced by local triggers: a case series and a proposal for diagnostic criteria based on a literature review.
Corbella-Bagot, Lluís; Gil-Lianes, Javier; Fernández-Vela, Javier; Martí-Martí, Ignasi; Alegre-Fernández, Marta; Fuertes, Irene; Garbayo-Salmons, Patricia; Bosch-Amate, Xavier; Guilabert, Antonio; Mascaró, José M.
Afiliação
  • Corbella-Bagot L; Department of Dermatology, Hospital Clínic de Barcelona, University of Barcelona, Barcelona, Spain.
  • Gil-Lianes J; Department of Dermatology, Hospital Clínic de Barcelona, University of Barcelona, Barcelona, Spain.
  • Fernández-Vela J; Department of Dermatology, Hospital General de Granollers, Granollers, Spain.
  • Martí-Martí I; Department of Dermatology, Hospital Clínic de Barcelona, University of Barcelona, Barcelona, Spain.
  • Alegre-Fernández M; Department of Dermatology, Hospital Clínic de Barcelona, University of Barcelona, Barcelona, Spain.
  • Fuertes I; Department of Dermatology, Hospital Clínic de Barcelona, University of Barcelona, Barcelona, Spain.
  • Garbayo-Salmons P; Department of Dermatology, Hospital Mútua de Terrassa, Terrassa, Spain.
  • Bosch-Amate X; Department of Dermatology, Hospital Clínic de Barcelona, University of Barcelona, Barcelona, Spain.
  • Guilabert A; Department of Dermatology, Hospital General de Granollers, Granollers, Spain.
  • Mascaró JM; Department of Dermatology, Hospital Clínic de Barcelona, University of Barcelona, Barcelona, Spain.
Front Immunol ; 14: 1160779, 2023.
Article em En | MEDLINE | ID: mdl-37334352
ABSTRACT

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.

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.

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.

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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dermatopatias Vesiculobolhosas / Penfigoide Bolhoso Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies Limite: Female / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dermatopatias Vesiculobolhosas / Penfigoide Bolhoso Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies Limite: Female / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article