Intravenous immunoglobulin treatment stabilizing a patient with Anti-PL7 antisynthetase syndrome with interstitial lung disease and eosinophilic inflammation.
Anti-PL7
Antisynthetase syndrome (AS)
Eosinophilic inflammation
Interstitial lung disease (ILD)
Intravenous immunoglobulin (IVIG)
Journal
Respiratory medicine case reports
ISSN: 2213-0071
Titre abrégé: Respir Med Case Rep
Pays: England
ID NLM: 101604463
Informations de publication
Date de publication:
2022
2022
Historique:
received:
07
02
2022
revised:
24
05
2022
accepted:
06
06
2022
entrez:
11
7
2022
pubmed:
12
7
2022
medline:
12
7
2022
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 35814032
doi: 10.1016/j.rmcr.2022.101686
pii: S2213-0071(22)00108-3
pmc: PMC9256658
doi:
Types de publication
Case Reports
Langues
eng
Pagination
101686Informations de copyright
© 2022 The Authors.
Déclaration de conflit d'intérêts
None.
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