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Three case reports of post immunization and post viral Bullous Pemphigoid: looking for the right trigger
BACKGROUND: Bullous pemphigoid (BP) is a blistering skin disorder infrequent in infancy and rarely reported in medical literature. CASE PRESENTATION: Here we describe three cases of BP which were referred to our department in the last 15 years. Two of them developed an eruption of bullous lesions ju...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5322655/ https://www.ncbi.nlm.nih.gov/pubmed/28228112 http://dx.doi.org/10.1186/s12887-017-0813-0 |
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author | Baroero, Luca Coppo, Paola Bertolino, Laura Maccario, Stefano Savino, Francesco |
author_facet | Baroero, Luca Coppo, Paola Bertolino, Laura Maccario, Stefano Savino, Francesco |
author_sort | Baroero, Luca |
collection | PubMed |
description | BACKGROUND: Bullous pemphigoid (BP) is a blistering skin disorder infrequent in infancy and rarely reported in medical literature. CASE PRESENTATION: Here we describe three cases of BP which were referred to our department in the last 15 years. Two of them developed an eruption of bullous lesions just a few days after vaccination for diphtheria, tetanus, pertussis, poliomyelitis, hepatitis B and Haemophilus influenzae B. The third patient developed the same blistering lesions shortly after herpetic stomatitis. In all three cases, clinical diagnosis was confirmed by histological examination which showed subepidermal bullae with a dermal inflammatory infiltrate, and direct immunofluorescence of perilesional skin showed linear IgG and C3 deposits along the basement membrane zone. Immunoblot assay was positive for BP antigen 180. Treatment with oral prednisone was instituted and the lesions resolved in two out of three patients; the third one was treated with an immunosuppressive agent (tacrolimus) and corticosteroid and subsequently with intravenous immunoglobulin and plasmapheresis, due to an underlying complex autoimmune disease. CONCLUSION: Although the mechanism of induction of BP is still unclear, the close relationship between trigger events (immunization or viral infection) and onset of the disease arises a possible association. |
format | Online Article Text |
id | pubmed-5322655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53226552017-03-01 Three case reports of post immunization and post viral Bullous Pemphigoid: looking for the right trigger Baroero, Luca Coppo, Paola Bertolino, Laura Maccario, Stefano Savino, Francesco BMC Pediatr Case Report BACKGROUND: Bullous pemphigoid (BP) is a blistering skin disorder infrequent in infancy and rarely reported in medical literature. CASE PRESENTATION: Here we describe three cases of BP which were referred to our department in the last 15 years. Two of them developed an eruption of bullous lesions just a few days after vaccination for diphtheria, tetanus, pertussis, poliomyelitis, hepatitis B and Haemophilus influenzae B. The third patient developed the same blistering lesions shortly after herpetic stomatitis. In all three cases, clinical diagnosis was confirmed by histological examination which showed subepidermal bullae with a dermal inflammatory infiltrate, and direct immunofluorescence of perilesional skin showed linear IgG and C3 deposits along the basement membrane zone. Immunoblot assay was positive for BP antigen 180. Treatment with oral prednisone was instituted and the lesions resolved in two out of three patients; the third one was treated with an immunosuppressive agent (tacrolimus) and corticosteroid and subsequently with intravenous immunoglobulin and plasmapheresis, due to an underlying complex autoimmune disease. CONCLUSION: Although the mechanism of induction of BP is still unclear, the close relationship between trigger events (immunization or viral infection) and onset of the disease arises a possible association. BioMed Central 2017-02-23 /pmc/articles/PMC5322655/ /pubmed/28228112 http://dx.doi.org/10.1186/s12887-017-0813-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Baroero, Luca Coppo, Paola Bertolino, Laura Maccario, Stefano Savino, Francesco Three case reports of post immunization and post viral Bullous Pemphigoid: looking for the right trigger |
title | Three case reports of post immunization and post viral Bullous Pemphigoid: looking for the right trigger |
title_full | Three case reports of post immunization and post viral Bullous Pemphigoid: looking for the right trigger |
title_fullStr | Three case reports of post immunization and post viral Bullous Pemphigoid: looking for the right trigger |
title_full_unstemmed | Three case reports of post immunization and post viral Bullous Pemphigoid: looking for the right trigger |
title_short | Three case reports of post immunization and post viral Bullous Pemphigoid: looking for the right trigger |
title_sort | three case reports of post immunization and post viral bullous pemphigoid: looking for the right trigger |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5322655/ https://www.ncbi.nlm.nih.gov/pubmed/28228112 http://dx.doi.org/10.1186/s12887-017-0813-0 |
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