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.
References in periodicals archive ?
Adult-onset Still's disease (AOSD) is a rare autoinflammatory disorder with typical features of spiking fever, evanescent rash, and arthritis/ arthralgia.
Adult-onset Still's disease associated to toxoplasma gondii infection.
Adult-onset Still's disease (AOSD) is a systemic inflammatory disorder characterized by high fever, arthralgia, transient rash, hepatosplenomegaly, lymphadenopathy, liver dysfunction, and leukocytosis.
A case of refractory adult-onset Still's disease with high serum Interleukin-18 levels treated with monitoring of serum levels of cyclosporine.
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.
The diagnosis of adult-onset Still's disease was then determined on the basis of clinical and laboratory criteria.
Adult-onset Still's disease (AOSD) is a rare systemic inflammatory disease with unknown origin and pathogenesis.
A case of paraneoplastic syndrome mimicking adult-onset Still's disease.
Adult-onset Still's disease seems to be one of the systemic rheumatological diseases that cause this syndrome.
In a single case report, abatacept was effective in treating adult-onset Still's disease, with the patient in remission after 35 months of therapy.
Tocilizumab for multirefractory adult-onset Still's disease.

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