Capillary basement membrane reduplication in myositis patients with mild clinical features of systemic sclerosis supports the concept of ‘scleromyositis’
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00401-021-02335-x.pdf
Reference12 articles.
1. Siegert E, Uruha A, Goebel H-H et al (2021) Systemic sclerosis-associated myositis features minimal inflammation and characteristic capillary pathology. Acta Neuropathol (Berl) 141:917–927. https://doi.org/10.1007/s00401-021-02305-3
2. Landon-Cardinal O, Leclair V, Troyanov Y, et al (2020) Scleromyositis is associated with distinct muscle vasculopathic features [abstract]. Arthritis Rheumatol 72 (suppl 10)
3. van den Hoogen F, Khanna D, Fransen J et al (2013) 2013 classification criteria for systemic sclerosis: an American college of rheumatology/European league against rheumatism collaborative initiative. Ann Rheum Dis 72:1747–1755. https://doi.org/10.1136/annrheumdis-2013-204424
4. Johnson SR, Fransen J, Khanna D et al (2012) Validation of potential classification criteria for systemic sclerosis. Arthritis Care Res 64:358–367. https://doi.org/10.1002/acr.20684
5. Lundberg IE, Tjärnlund A, Bottai M et al (2017) 2017 European League Against Rheumatism/American College of rheumatology classification criteria for adult and juvenile idiopathic inflammatory myopathies and their major subgroups. Arthritis Rheumatol Hoboken NJ 69:2271–2282. https://doi.org/10.1002/art.40320
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