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May Bacterial Infections Trigger Bullous Pemphigoid? Case Report and Review of Literature
Bullous pemphigoid (BP) is an autoimmune blistering skin disease, mainly observed in the elderly. Infections have been suggested as possible disease triggers. However, infections may even heavily influence the disease clinical course and mortality. A 75-year-old woman was admitted to hospital for se...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8229970/ https://www.ncbi.nlm.nih.gov/pubmed/34200214 http://dx.doi.org/10.3390/microorganisms9061235 |
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author | Biondo, Michela Ileen Fiorentino, Chiara Persechino, Severino Tammaro, Antonella Koverech, Angela Bartolazzi, Armando Raffa, Salvatore Canzoni, Marco Picchianti-Diamanti, Andrea Di Rosa, Roberta Di Zenzo, Giovanni Scala, Enrico Meneguzzi, Giorgia Ferlito, Claudia Markovic, Milica Caporuscio, Sara Sorgi, Maria Laura Salemi, Simonetta Laganà, Bruno |
author_facet | Biondo, Michela Ileen Fiorentino, Chiara Persechino, Severino Tammaro, Antonella Koverech, Angela Bartolazzi, Armando Raffa, Salvatore Canzoni, Marco Picchianti-Diamanti, Andrea Di Rosa, Roberta Di Zenzo, Giovanni Scala, Enrico Meneguzzi, Giorgia Ferlito, Claudia Markovic, Milica Caporuscio, Sara Sorgi, Maria Laura Salemi, Simonetta Laganà, Bruno |
author_sort | Biondo, Michela Ileen |
collection | PubMed |
description | Bullous pemphigoid (BP) is an autoimmune blistering skin disease, mainly observed in the elderly. Infections have been suggested as possible disease triggers. However, infections may even heavily influence the disease clinical course and mortality. A 75-year-old woman was admitted to hospital for severe erythematosus blistering disease, accompanied by hyper-eosinophilia and hyper-IgE. The culture of bullous fluid was positive for Enterococcus faecalis, the blood culture was positive for Staphylococcus aureus, and the urine culture was positive for Proteus mirabilis and Escherichia coli. Moreover, circulating anti-BP180 IgG was present and the histopathological/ultrastructural examination of a lesional skin biopsy was compatible with BP. High eosinophil levels (up to 3170/µL) were found throughout the clinical course, while values below 1000/µL were associated with clinical improvement. The total IgE was 1273 IU/mL, and specific anti-G/V-penicillin/ampicillin IgE antibodies were positive. The patient had a complete clinical recovery in two months with methyl-prednisolone (40 then 20 mg/day) and low-dose azathioprine (50 mg/day) as a steroid-sparing agent. The steroid treatment was tapered until interruption during a one-year period and intravenous immunoglobulins have been administered for three years in order for azathioprine to also be interrupted. The patient stopped any treatment five years ago and, in this period, has always been in good health. In this case, the contemporaneous onset of different bacterial infections and BP is suggestive of bacterial infections acting as BP trigger(s), with allergic and autoimmune pathways contributing to the disease pathogenesis. |
format | Online Article Text |
id | pubmed-8229970 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82299702021-06-26 May Bacterial Infections Trigger Bullous Pemphigoid? Case Report and Review of Literature Biondo, Michela Ileen Fiorentino, Chiara Persechino, Severino Tammaro, Antonella Koverech, Angela Bartolazzi, Armando Raffa, Salvatore Canzoni, Marco Picchianti-Diamanti, Andrea Di Rosa, Roberta Di Zenzo, Giovanni Scala, Enrico Meneguzzi, Giorgia Ferlito, Claudia Markovic, Milica Caporuscio, Sara Sorgi, Maria Laura Salemi, Simonetta Laganà, Bruno Microorganisms Case Report Bullous pemphigoid (BP) is an autoimmune blistering skin disease, mainly observed in the elderly. Infections have been suggested as possible disease triggers. However, infections may even heavily influence the disease clinical course and mortality. A 75-year-old woman was admitted to hospital for severe erythematosus blistering disease, accompanied by hyper-eosinophilia and hyper-IgE. The culture of bullous fluid was positive for Enterococcus faecalis, the blood culture was positive for Staphylococcus aureus, and the urine culture was positive for Proteus mirabilis and Escherichia coli. Moreover, circulating anti-BP180 IgG was present and the histopathological/ultrastructural examination of a lesional skin biopsy was compatible with BP. High eosinophil levels (up to 3170/µL) were found throughout the clinical course, while values below 1000/µL were associated with clinical improvement. The total IgE was 1273 IU/mL, and specific anti-G/V-penicillin/ampicillin IgE antibodies were positive. The patient had a complete clinical recovery in two months with methyl-prednisolone (40 then 20 mg/day) and low-dose azathioprine (50 mg/day) as a steroid-sparing agent. The steroid treatment was tapered until interruption during a one-year period and intravenous immunoglobulins have been administered for three years in order for azathioprine to also be interrupted. The patient stopped any treatment five years ago and, in this period, has always been in good health. In this case, the contemporaneous onset of different bacterial infections and BP is suggestive of bacterial infections acting as BP trigger(s), with allergic and autoimmune pathways contributing to the disease pathogenesis. MDPI 2021-06-07 /pmc/articles/PMC8229970/ /pubmed/34200214 http://dx.doi.org/10.3390/microorganisms9061235 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Biondo, Michela Ileen Fiorentino, Chiara Persechino, Severino Tammaro, Antonella Koverech, Angela Bartolazzi, Armando Raffa, Salvatore Canzoni, Marco Picchianti-Diamanti, Andrea Di Rosa, Roberta Di Zenzo, Giovanni Scala, Enrico Meneguzzi, Giorgia Ferlito, Claudia Markovic, Milica Caporuscio, Sara Sorgi, Maria Laura Salemi, Simonetta Laganà, Bruno May Bacterial Infections Trigger Bullous Pemphigoid? Case Report and Review of Literature |
title | May Bacterial Infections Trigger Bullous Pemphigoid? Case Report and Review of Literature |
title_full | May Bacterial Infections Trigger Bullous Pemphigoid? Case Report and Review of Literature |
title_fullStr | May Bacterial Infections Trigger Bullous Pemphigoid? Case Report and Review of Literature |
title_full_unstemmed | May Bacterial Infections Trigger Bullous Pemphigoid? Case Report and Review of Literature |
title_short | May Bacterial Infections Trigger Bullous Pemphigoid? Case Report and Review of Literature |
title_sort | may bacterial infections trigger bullous pemphigoid? case report and review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8229970/ https://www.ncbi.nlm.nih.gov/pubmed/34200214 http://dx.doi.org/10.3390/microorganisms9061235 |
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