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Linear IGA bullous dermatosis potentially triggered by vaccination

Linear IgA bullous dermatosis (LABD) is a mucocutaneous autoimmune blistering disease affecting both adults and children. It is caused by IgA antibodies targeting multiple antigens along the basement membrane zone, leading to disruption of dermoepidermal junction and development of bullous lesions w...

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Autores principales: Corrà, Alberto, Bonciolini, Veronica, Quintarelli, Lavinia, Verdelli, Alice, Caproni, Marzia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8753231/
https://www.ncbi.nlm.nih.gov/pubmed/35001680
http://dx.doi.org/10.1177/20587384211021218
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author Corrà, Alberto
Bonciolini, Veronica
Quintarelli, Lavinia
Verdelli, Alice
Caproni, Marzia
author_facet Corrà, Alberto
Bonciolini, Veronica
Quintarelli, Lavinia
Verdelli, Alice
Caproni, Marzia
author_sort Corrà, Alberto
collection PubMed
description Linear IgA bullous dermatosis (LABD) is a mucocutaneous autoimmune blistering disease affecting both adults and children. It is caused by IgA antibodies targeting multiple antigens along the basement membrane zone, leading to disruption of dermoepidermal junction and development of bullous lesions which often presents in characteristic arrangement. Although most LABD cases have been reported to be idiopathic, different triggers have been described, including several drugs and infection. However, the occurrence of vaccine-induced cases of LABD is not widely known and accepted due to the few reports available. We present two cases of LABD occurred following different triggers, rising the suspicion for a possible pathogenetic role of vaccines.
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spelling pubmed-87532312022-01-13 Linear IGA bullous dermatosis potentially triggered by vaccination Corrà, Alberto Bonciolini, Veronica Quintarelli, Lavinia Verdelli, Alice Caproni, Marzia Int J Immunopathol Pharmacol Case Report Linear IgA bullous dermatosis (LABD) is a mucocutaneous autoimmune blistering disease affecting both adults and children. It is caused by IgA antibodies targeting multiple antigens along the basement membrane zone, leading to disruption of dermoepidermal junction and development of bullous lesions which often presents in characteristic arrangement. Although most LABD cases have been reported to be idiopathic, different triggers have been described, including several drugs and infection. However, the occurrence of vaccine-induced cases of LABD is not widely known and accepted due to the few reports available. We present two cases of LABD occurred following different triggers, rising the suspicion for a possible pathogenetic role of vaccines. SAGE Publications 2022-01-10 /pmc/articles/PMC8753231/ /pubmed/35001680 http://dx.doi.org/10.1177/20587384211021218 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage)
spellingShingle Case Report
Corrà, Alberto
Bonciolini, Veronica
Quintarelli, Lavinia
Verdelli, Alice
Caproni, Marzia
Linear IGA bullous dermatosis potentially triggered by vaccination
title Linear IGA bullous dermatosis potentially triggered by vaccination
title_full Linear IGA bullous dermatosis potentially triggered by vaccination
title_fullStr Linear IGA bullous dermatosis potentially triggered by vaccination
title_full_unstemmed Linear IGA bullous dermatosis potentially triggered by vaccination
title_short Linear IGA bullous dermatosis potentially triggered by vaccination
title_sort linear iga bullous dermatosis potentially triggered by vaccination
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8753231/
https://www.ncbi.nlm.nih.gov/pubmed/35001680
http://dx.doi.org/10.1177/20587384211021218
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