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Adult-onset Still's disease (AOSD) is a form of Still's disease, a rare systemic autoinflammatory disease characterized by the classic triad of fevers, joint pain, and a distinctive salmon-colored bumpy rash. The disease is considered a diagnosis of exclusion. [1] Levels of the iron-binding protein ferritin may be extremely elevated with this ...
Still disease, Still's disease, sJIA, systemic juvenile idiopathic arthritis. [1] Specialty: Pediatrics, rheumatology: Symptoms: Fever, arthritis, rash, and lymphadenopathy. [2] Complications: Macrophage activation syndrome. [3] Usual onset: 1-5 years old. [2] Diagnostic method: Excluding other disorders and clinical criteria. [2] Differential ...
In addition, MAS has been described in association with systemic lupus erythematosus (SLE), Kawasaki disease, and adult-onset Still's disease. It is thought to be closely related and pathophysiologically very similar to reactive (secondary) hemophagocytic lymphohistiocytosis (HLH). [1]
Still's disease can refer to: Systemic-onset juvenile idiopathic arthritis; Adult-onset Still's disease This page was last edited on 29 July 2015, at 09:55 (UTC ...
In rheumatic diseases, this syndrome is more often referred to as macrophage activation syndrome (MAS) and occurs most frequently in the juvenile onset and adult onset forms of Still's disease and in systemic lupus erythematosus. It occurs rarely in juvenile idiopathic arthritis, juvenile Kawasaki disease, and rheumatoid arthritis. [7]
Now, the NFL star is opening up for the first time to PEOPLE about being diagnosed with a chronic skin disease that left his signature beard flaky and uncomfortable as he struggled to find a solution.
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Recent therapeutic advances in the management of JIA have made inactive disease and clinical remission achievable goals for the majority of children with access to modern treatments. Clinical remission can be defined as the absence of signs and symptoms of inflammatory disease activity, including extra-articular manifestations of the disease.