Results 21 to 30 of about 5,195 (140)
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
Gene-expression analysis of adult-onset Still’s disease and systemic juvenile idiopathic arthritis is consistent with a continuum of a single disease entity [PDF]
, 2015 Background: Adult-onset Still’s disease (AOSD), a rare autoinflammatory disorder, resembles systemic juvenile idiopathic arthritis (SJIA). The superimposable systemic clinical features of AOSD and SJIA suggest both clinical phenotypes represent the same ...
Blank, Norbert +8 more
core +3 more sources
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
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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
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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
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
Fever and erythema: exclude all and then… think of Still’s disease!
Italian Journal of Medicine, 2016 Adult-onset Still’s disease is a rare disease. Diagnosis of Still’s disease is often difficult to achieve. Herein, we describe our diagnostic approach in a case report regarding an adult patient who presented with fever, erythema, lymphadenopathy and ...
Marta Maset +5 more
doaj +1 more source
H-ferritin and proinflammatory cytokines are increased in the bone marrow of patients affected by macrophage activation syndrome [PDF]
, 2017 Macrophage activation syndrome (MAS) is hyperinflammatory life-threatening syndrome, associated typically with high levels of serum ferritin. This is an iron storage protein including heavy (H) and light (L) subunits, categorized on their molecular ...
Berardicurti, O. +9 more
core +1 more source
Adult-onset Still's disease with atypical cutaneous manifestations [PDF]
, 2018 The diagnosis of adult-onset Still's disease (AOSD) can be very difficult. There are no specific tests available, and diagnosis is usually based on a symptom complex and the well-described typical evanescent rash seen in the majority of patients. However,
Juarez, Pablo +6 more
core +1 more source