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...

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Main Authors: Michela Ileen Biondo, Chiara Fiorentino, Severino Persechino, Antonella Tammaro, Angela Koverech, Armando Bartolazzi, Salvatore Raffa, Marco Canzoni, Andrea Picchianti-Diamanti, Roberta Di Rosa, Giovanni Di Zenzo, Enrico Scala, Giorgia Meneguzzi, Claudia Ferlito, Milica Markovic, Sara Caporuscio, Maria Laura Sorgi, Simonetta Salemi, Bruno Laganà
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Microorganisms
Subjects:
Online Access:https://www.mdpi.com/2076-2607/9/6/1235
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author Michela Ileen Biondo
Chiara Fiorentino
Severino Persechino
Antonella Tammaro
Angela Koverech
Armando Bartolazzi
Salvatore Raffa
Marco Canzoni
Andrea Picchianti-Diamanti
Roberta Di Rosa
Giovanni Di Zenzo
Enrico Scala
Giorgia Meneguzzi
Claudia Ferlito
Milica Markovic
Sara Caporuscio
Maria Laura Sorgi
Simonetta Salemi
Bruno Laganà
author_facet Michela Ileen Biondo
Chiara Fiorentino
Severino Persechino
Antonella Tammaro
Angela Koverech
Armando Bartolazzi
Salvatore Raffa
Marco Canzoni
Andrea Picchianti-Diamanti
Roberta Di Rosa
Giovanni Di Zenzo
Enrico Scala
Giorgia Meneguzzi
Claudia Ferlito
Milica Markovic
Sara Caporuscio
Maria Laura Sorgi
Simonetta Salemi
Bruno Laganà
author_sort Michela Ileen Biondo
collection DOAJ
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 <i>Enterococcus faecalis</i>, the blood culture was positive for <i>Staphylococcus aureus</i>, and the urine culture was positive for <i>Proteus mirabilis</i> and <i>Escherichia coli.</i> 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.
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spelling doaj.art-33270419636945cb9a8e5e053ee4998a2023-11-21T23:04:14ZengMDPI AGMicroorganisms2076-26072021-06-0196123510.3390/microorganisms9061235May Bacterial Infections Trigger Bullous Pemphigoid? Case Report and Review of LiteratureMichela Ileen Biondo0Chiara Fiorentino1Severino Persechino2Antonella Tammaro3Angela Koverech4Armando Bartolazzi5Salvatore Raffa6Marco Canzoni7Andrea Picchianti-Diamanti8Roberta Di Rosa9Giovanni Di Zenzo10Enrico Scala11Giorgia Meneguzzi12Claudia Ferlito13Milica Markovic14Sara Caporuscio15Maria Laura Sorgi16Simonetta Salemi17Bruno Laganà18Dipartimento di Medicina Clinica e Molecolare, Sapienza, Università di Roma, AOU S. Andrea, 00189 Roma, ItalyDipartimento di Medicina Clinica e Molecolare, Sapienza, Università di Roma, AOU S. Andrea, 00189 Roma, ItalyUOD di Dermatologia, Sapienza, Università di Roma, AOU S. Andrea, 00189 Roma, ItalyUOD di Dermatologia, Sapienza, Università di Roma, AOU S. Andrea, 00189 Roma, ItalyDipartimento di Medicina Clinica e Molecolare, Sapienza, Università di Roma, AOU S. Andrea, 00189 Roma, ItalyDipartimento di Medicina Clinica e Molecolare, Sapienza, Università di Roma, AOU S. Andrea, 00189 Roma, ItalyDipartimento di Medicina Clinica e Molecolare, Sapienza, Università di Roma, AOU S. Andrea, 00189 Roma, ItalyDipartimento di Medicina Clinica e Molecolare, Sapienza, Università di Roma, AOU S. Andrea, 00189 Roma, ItalyDipartimento di Medicina Clinica e Molecolare, Sapienza, Università di Roma, AOU S. Andrea, 00189 Roma, ItalyDipartimento di Medicina Clinica e Molecolare, Sapienza, Università di Roma, AOU S. Andrea, 00189 Roma, ItalyIstituto Dermopatico dell’Immacolata, 00167 Roma, ItalyIstituto Dermopatico dell’Immacolata, 00167 Roma, ItalyDipartimento di Medicina Clinica e Molecolare, Sapienza, Università di Roma, AOU S. Andrea, 00189 Roma, ItalyDipartimento di Medicina Clinica e Molecolare, Sapienza, Università di Roma, AOU S. Andrea, 00189 Roma, ItalyDipartimento di Medicina Clinica e Molecolare, Sapienza, Università di Roma, AOU S. Andrea, 00189 Roma, ItalyDipartimento di Medicina Clinica e Molecolare, Sapienza, Università di Roma, AOU S. Andrea, 00189 Roma, ItalyDipartimento di Medicina Clinica e Molecolare, Sapienza, Università di Roma, AOU S. Andrea, 00189 Roma, ItalyDipartimento di Medicina Clinica e Molecolare, Sapienza, Università di Roma, AOU S. Andrea, 00189 Roma, ItalyDipartimento di Medicina Clinica e Molecolare, Sapienza, Università di Roma, AOU S. Andrea, 00189 Roma, ItalyBullous 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 <i>Enterococcus faecalis</i>, the blood culture was positive for <i>Staphylococcus aureus</i>, and the urine culture was positive for <i>Proteus mirabilis</i> and <i>Escherichia coli.</i> 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.https://www.mdpi.com/2076-2607/9/6/1235bullous pemphigoid (BP)infectionsautoimmunityIVIg
spellingShingle Michela Ileen Biondo
Chiara Fiorentino
Severino Persechino
Antonella Tammaro
Angela Koverech
Armando Bartolazzi
Salvatore Raffa
Marco Canzoni
Andrea Picchianti-Diamanti
Roberta Di Rosa
Giovanni Di Zenzo
Enrico Scala
Giorgia Meneguzzi
Claudia Ferlito
Milica Markovic
Sara Caporuscio
Maria Laura Sorgi
Simonetta Salemi
Bruno Laganà
May Bacterial Infections Trigger Bullous Pemphigoid? Case Report and Review of Literature
Microorganisms
bullous pemphigoid (BP)
infections
autoimmunity
IVIg
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 bullous pemphigoid (BP)
infections
autoimmunity
IVIg
url https://www.mdpi.com/2076-2607/9/6/1235
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