Idiopathic inflammatory myopathies: one year in review 2022.
Journal
Clinical and experimental rheumatology
ISSN: 0392-856X
Titre abrégé: Clin Exp Rheumatol
Pays: Italy
ID NLM: 8308521
Informations de publication
Date de publication:
Mar 2023
Mar 2023
Historique:
received:
04
01
2023
accepted:
06
01
2023
pubmed:
25
2
2023
medline:
4
3
2023
entrez:
24
2
2023
Statut:
ppublish
Résumé
Idiopathic inflammatory myopathies (IIM) are a heterogeneous group of disorders in which chronic inflammation of the skeletal muscle, leading to muscle weakness, is a common feature. Different phenotypes have been identified within the IIM spectrum based on extra-muscular manifestations, immunology, muscle histology, responsiveness to therapy, and prognosis. The pathogenesis, classification, treatment, and prognosis of the different IIM subtypes are subject to active discussion and research. This review highlights the most relevant literature published on this topic over the last year.
Identifiants
pubmed: 36826800
pii: 19544
doi: 10.55563/clinexprheumatol/jof6qn
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM