adult-onset Still's disease

adult-onset Still's disease

Rheumatology Still's disease–acute febrile onset of arthritis in adults Clinical Multiple remissions and exacerbations, loss of wrist extension, carpal ankylosis, distal interphalangeal joint involvement; other features include daily fever spikes, loss of neck motion, evanescent pink macules most prominent when febrile, pericarditis, pleural effusions, severe abdominal pain Lab Normal rheumatoid factor, ANA, complement See Rheumatoid arthritis, Still's disease.
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She had been put into a medically induced coma after coming down with an extremely rare illness, adult-onset Still's disease.
Adult-onset Still's disease (AOSD) and systemic juvenile idiopathic arthritis (SJIA) are rare systemic disorders of auto-inflammatory nature.
Adult-onset Still's disease (AOSD) is an auto-inflammatory disorder, characterized by spiking fevers, evanescent salmon-pink rash, arthritis or arthralgia, and hyperleukocytosis.
In August 2016, the European Commission approved Ilaris for a license extension to also treat patients with Adult-Onset Still's Disease (AOSD).
Life-threatening complications of adult-onset Still's disease.
Adult-onset Still's disease (AOSD) is a systemic inflammatory disorder characterized by high fever, arthralgia, transient rash, hepatosplenomegaly, lymphadenopathy, liver dysfunction, and leukocytosis.
The presence of systemic symptoms could mean the urticarial rash is not ordinary urticaria," he said, suggesting that vasculitis, Schitzler's syndrome, adult-onset Still's disease, an autoinflammatory syndrome, or urticarial dermatitis could be at play.
It is associated with infections (eg, Epstein-Barr virus (EBV), cytomegalovirus, herpes simplex virus, avian influenza, rhematologic diseases (eg, systemic lupus erythamatosis, Kawasaki syndrome, adult-onset Still's disease, rheumatoid arthritis and others, malignancy (eg, natural killer [NK]-cell leukemia, peripheral T-cell lymphoma, EBV in T cell lymphoma, B-cell lymphoma, and a variety of other lymphomas, acquired immune deficiency state (eg, after organ transplantation), and pharmacotherapy.
Adult-onset Still's disease (AOSD) is a rare systemic inflammatory disease with unknown origin and pathogenesis.

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