Results 1 to 10 of about 2,775 (239)
Adult‐onset Still's disease complicated by macrophage activation syndrome
Clinical Case Reports, 2023 Key Clinical Message Young patients with persistent rash and fevers despite antibiotic treatment should be evaluated for non‐infectious etiologies. In our patient's case, these findings led to a diagnosis of MAS, which ultimately affected how she was ...
Toluwalase Awoyemi +2 more
doaj +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
Critical Care Explorations, 2021 BACKGROUND:. We report a case of a young woman with adult-onset Still’s disease presenting as macrophage-activation syndrome complicated by shock and respiratory failure during the third trimester of pregnancy. CASE SUMMARY:. A previously healthy 26-year-
Andrew T. Peters, MD +1 more
doaj +1 more source
Tocilizumab for the treatment of adult-onset Still’s disease [PDF]
Expert Opinion on Biological Therapy, 2019 Adult-onset Still´s disease (AOSD) is a systemic inflammatory condition that affects mainly young people. The clinical course consists of two distinctive patterns: one with a predominance of systemic symptoms and another manifested by progressive chronic polyarthritis. Glucocorticoids remain the mainstay in the treatment of AOSD.
Castañeda, Santos +5 more
openaire +3 more sources
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
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
doaj +1 more source
Myocarditis in Adult-Onset Still Disease
Medicine, 2014 This study highlights the clinical features, treatments, and outcomes of the rare myocarditis in adult-onset Still disease (AOSD). Among a case series of 57 patients fulfilling either Yamaguchi or Fautrel AOSD criteria and seen between 1998 and 2010, we identified 4 cases of myocarditis.
Gerfaud-Valentin, Mathieu +7 more
openaire +2 more sources
Anakinra for the treatment of adult-onset Still’s disease [PDF]
Expert Review of Clinical Immunology, 2018 Adult onset Still's disease (AOSD) is an uncommon systemic inflammatory disease on the clinical spectrum of autoinflammatory disorders. Its presentation and clinical course may result in several well-differentiated phenotypes: from a systemic and highly symptomatic pattern to a chronic articular pattern.
Castañeda Sanz, Santos +4 more
openaire +3 more sources
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