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Intravenous immunoglobulin treatment stabilizing a patient with Anti-PL7 antisynthetase syndrome with interstitial lung disease and eosinophilic inflammation

Antisynthetase syndrome (AS) is a rare autoimmune disease characterized by autoantibodies against aminoacyl-transfer RNA synthetase and clinical features which can include interstitial lung disease (ILD). Current available evidence of treatment is based on expert opinions and case reports. Here, we...

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Autores principales: Peshbahar, Soran, Hyldgaard, Charlotte, Bendstrup, Elisabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9256658/
https://www.ncbi.nlm.nih.gov/pubmed/35814032
http://dx.doi.org/10.1016/j.rmcr.2022.101686
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author Peshbahar, Soran
Hyldgaard, Charlotte
Bendstrup, Elisabeth
author_facet Peshbahar, Soran
Hyldgaard, Charlotte
Bendstrup, Elisabeth
author_sort Peshbahar, Soran
collection PubMed
description Antisynthetase syndrome (AS) is a rare autoimmune disease characterized by autoantibodies against aminoacyl-transfer RNA synthetase and clinical features which can include interstitial lung disease (ILD). Current available evidence of treatment is based on expert opinions and case reports. Here, we present a patient with an initial diagnosis of eosinophilic pneumonia, who was later diagnosed with anti-PL7 antisynthetase syndrome with ILD and eosinophilic inflammation. The patient was non-responsive to classic immunosuppressants but responded remarkably well to intravenous immunoglobulin.
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spelling pubmed-92566582022-07-07 Intravenous immunoglobulin treatment stabilizing a patient with Anti-PL7 antisynthetase syndrome with interstitial lung disease and eosinophilic inflammation Peshbahar, Soran Hyldgaard, Charlotte Bendstrup, Elisabeth Respir Med Case Rep Case Report Antisynthetase syndrome (AS) is a rare autoimmune disease characterized by autoantibodies against aminoacyl-transfer RNA synthetase and clinical features which can include interstitial lung disease (ILD). Current available evidence of treatment is based on expert opinions and case reports. Here, we present a patient with an initial diagnosis of eosinophilic pneumonia, who was later diagnosed with anti-PL7 antisynthetase syndrome with ILD and eosinophilic inflammation. The patient was non-responsive to classic immunosuppressants but responded remarkably well to intravenous immunoglobulin. Elsevier 2022-06-14 /pmc/articles/PMC9256658/ /pubmed/35814032 http://dx.doi.org/10.1016/j.rmcr.2022.101686 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Peshbahar, Soran
Hyldgaard, Charlotte
Bendstrup, Elisabeth
Intravenous immunoglobulin treatment stabilizing a patient with Anti-PL7 antisynthetase syndrome with interstitial lung disease and eosinophilic inflammation
title Intravenous immunoglobulin treatment stabilizing a patient with Anti-PL7 antisynthetase syndrome with interstitial lung disease and eosinophilic inflammation
title_full Intravenous immunoglobulin treatment stabilizing a patient with Anti-PL7 antisynthetase syndrome with interstitial lung disease and eosinophilic inflammation
title_fullStr Intravenous immunoglobulin treatment stabilizing a patient with Anti-PL7 antisynthetase syndrome with interstitial lung disease and eosinophilic inflammation
title_full_unstemmed Intravenous immunoglobulin treatment stabilizing a patient with Anti-PL7 antisynthetase syndrome with interstitial lung disease and eosinophilic inflammation
title_short Intravenous immunoglobulin treatment stabilizing a patient with Anti-PL7 antisynthetase syndrome with interstitial lung disease and eosinophilic inflammation
title_sort intravenous immunoglobulin treatment stabilizing a patient with anti-pl7 antisynthetase syndrome with interstitial lung disease and eosinophilic inflammation
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9256658/
https://www.ncbi.nlm.nih.gov/pubmed/35814032
http://dx.doi.org/10.1016/j.rmcr.2022.101686
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