Results 21 to 30 of about 103,363 (247)
Rheumatology, 2022 Objective To compare clinical features and treatments of patients with systemic JIA (sIJA) and adult-onset Still’s disease (AOSD). Methods The clinical charts of consecutive patients with sJIA by International League of Association of Rheumatology ...
P. Ruscitti +32 more
semanticscholar +1 more source
Annals of the Rheumatic Diseases, 2018 Objective To evaluate the efficacy and safety of tocilizumab, an interleukin-6 receptor antibody, in patients with adult-onset Still’s disease. Methods In this double-blind, randomised, placebo-controlled phase III trial, 27 patients with adult-onset ...
Y. Kaneko +8 more
semanticscholar +1 more source
Adult-onset Still’s disease: A disease at the crossroad of innate immunity and autoimmunity
Frontiers in Medicine, 2022 Adult-onset Still’s disease (AOSD) is a rare disease affecting multiple systems and organs with unknown etiology, and the clinical symptoms are usually described as spiking fever, arthritis, evanescent salmon-pink eruptions, lymphadenopathy, splenomegaly,
Shijia Rao +4 more
semanticscholar +1 more source
Non-Hodgkin's lymphoma in a woman with adult-onset Still's disease: a case report
Journal of Medical Case Reports, 2008 Introduction Adult onset Still's disease is a chronic multisystemic inflammatory disorder characterized by high spiking fever, polyarthralgia and rash.
Otrock Zaher K +5 more
doaj +1 more source
A case of adult‐onset Still's disease in a patient after a car accident
Clinical Case Reports, 2023 Key Clinical Message Adult‐onset Still's disease is a rare inflammatory condition with diverse clinical features. Yamaguchi criteria aid diagnosis, and pleural effusion and elevated ferritin levels are important markers.
Feride Yaman, Ali Kimiaei
doaj +1 more source
Biomarkers for adult-onset Still’s disease
Научно-практическая ревматология, 2022 Adult-onset Still’s disease (AOSD) is a rare complex autoinflammatory disease of unknown etiology. The main problem, practitioners have been facing with when researching AOSD, is the lack of developed approaches to assessing the activity of the disease ...
V. Yu. Myachikova +4 more
doaj +1 more source
Autoimmunity Reviews, 2014 First described in 1971, adult-onset Still's disease (AOSD) is a rare multisystemic disorder considered as a complex (multigenic) autoinflammatory syndrome. A genetic background would confer susceptibility to the development of autoinflammatory reactions
Mathieu Gerfaud-Valentin +3 more
semanticscholar +1 more source
Suppurative necrotizing granulomatous lymphadenitis in adult-onset Still’s disease: a case report
Journal of Medical Case Reports, 2012 Introduction Lymphadenopathy is found in about 65% of patients with adult-onset Still’s disease and is histologically characterized by an intense, paracortical immunoblastic hyperplasia. Adult-onset Still’s disease has not been previously described as an
Assimakopoulos Stelios F +5 more
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Acta Dermato-Venereologica, 2021 Persistent eruption occurs in a subset of patients with adult-onset Still’s disease. In our experience, a considerable proportion of these patients present with peripheral eosinophilia.
Jia-Wei Liu +6 more
doaj +1 more source
Arthritis Research & Therapy, 2019 BackgroundAdult-onset Still’s disease (AOSD) is a systemic inflammatory disease characterized by neutrophilia and NLRP3 inflammasome and macrophage activation. We investigated the role of neutrophil extracellular traps (NETs) in the pathogenesis of AOSD,
Qiong-yi Hu +16 more
semanticscholar +1 more source