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Bullous Pemphigoid Associated with Multiple System Atrophy: Case Series

BACKGROUND: Bullous pemphigoid (BP) is an autoimmune blistering dermatosis associated with a number of neurological conditions, including idiopathic Parkinson's disease (IPD). Only 1 case of BP in a patient with multiple system atrophy (MSA) has been reported. CASES: We report 3 cases of men wi...

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Detalles Bibliográficos
Autores principales: Snedden, Andrew, Sharif, Jennifer, Newsham, John, Kobylecki, Christopher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015901/
https://www.ncbi.nlm.nih.gov/pubmed/33816675
http://dx.doi.org/10.1002/mdc3.13160
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author Snedden, Andrew
Sharif, Jennifer
Newsham, John
Kobylecki, Christopher
author_facet Snedden, Andrew
Sharif, Jennifer
Newsham, John
Kobylecki, Christopher
author_sort Snedden, Andrew
collection PubMed
description BACKGROUND: Bullous pemphigoid (BP) is an autoimmune blistering dermatosis associated with a number of neurological conditions, including idiopathic Parkinson's disease (IPD). Only 1 case of BP in a patient with multiple system atrophy (MSA) has been reported. CASES: We report 3 cases of men with probable MSA who developed bullous pemphigoid at a latency of 4–6 years from MSA symptom onset. CONCLUSIONS: Skin α‐synuclein deposition in neurodegenerative conditions such as IPD and MSA may be a potential substrate for the exposure of BP‐related antigens. Alternatively, central neurodegeneration may expose antigens as a substrate for cross‐reactivity and BP pathogenesis. Our report suggests an association between BP and MSA, in addition to the previously documented association with IPD.
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spelling pubmed-80159012021-04-02 Bullous Pemphigoid Associated with Multiple System Atrophy: Case Series Snedden, Andrew Sharif, Jennifer Newsham, John Kobylecki, Christopher Mov Disord Clin Pract Case Series BACKGROUND: Bullous pemphigoid (BP) is an autoimmune blistering dermatosis associated with a number of neurological conditions, including idiopathic Parkinson's disease (IPD). Only 1 case of BP in a patient with multiple system atrophy (MSA) has been reported. CASES: We report 3 cases of men with probable MSA who developed bullous pemphigoid at a latency of 4–6 years from MSA symptom onset. CONCLUSIONS: Skin α‐synuclein deposition in neurodegenerative conditions such as IPD and MSA may be a potential substrate for the exposure of BP‐related antigens. Alternatively, central neurodegeneration may expose antigens as a substrate for cross‐reactivity and BP pathogenesis. Our report suggests an association between BP and MSA, in addition to the previously documented association with IPD. John Wiley & Sons, Inc. 2021-02-25 /pmc/articles/PMC8015901/ /pubmed/33816675 http://dx.doi.org/10.1002/mdc3.13160 Text en © 2021 The Authors. Movement Disorders Clinical Practice published by Wiley Periodicals LLC. on behalf of International Parkinson and Movement Disorder Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Series
Snedden, Andrew
Sharif, Jennifer
Newsham, John
Kobylecki, Christopher
Bullous Pemphigoid Associated with Multiple System Atrophy: Case Series
title Bullous Pemphigoid Associated with Multiple System Atrophy: Case Series
title_full Bullous Pemphigoid Associated with Multiple System Atrophy: Case Series
title_fullStr Bullous Pemphigoid Associated with Multiple System Atrophy: Case Series
title_full_unstemmed Bullous Pemphigoid Associated with Multiple System Atrophy: Case Series
title_short Bullous Pemphigoid Associated with Multiple System Atrophy: Case Series
title_sort bullous pemphigoid associated with multiple system atrophy: case series
topic Case Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015901/
https://www.ncbi.nlm.nih.gov/pubmed/33816675
http://dx.doi.org/10.1002/mdc3.13160
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