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.

Mentioned in ?

References in periodicals archive ?

She had been put into a medically induced coma after coming down with an extremely rare illness, adult-onset Still's disease.

Kumail Nanjiani talks cultural challenges and racist hecklers

Adult-onset Still's disease (AOSD) and systemic juvenile idiopathic arthritis (SJIA) are rare systemic disorders of auto-inflammatory nature.

Sobi investigates the safety and efficacy of anakinra in patient with Still's disease under phase 3 clinical study

Adult-onset Still's disease (AOSD) is an auto-inflammatory disorder, characterized by spiking fevers, evanescent salmon-pink rash, arthritis or arthralgia, and hyperleukocytosis.

Occurrence of Ulcerative Colitis in a Patient With Adult-Onset Still's Disease: Coincidence or Correlated

In August 2016, the European Commission approved Ilaris for a license extension to also treat patients with Adult-Onset Still's Disease (AOSD).

Switzerland : Novartis receives three new FDA approvals for the expanded use of Ilaris treating rare Periodic Fever Syndrome conditions

Life-threatening complications of adult-onset Still's disease.

A case of atypical urticaria

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 adult-onset still's disease treated with monitoring of serum tacrolimus levels

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.

Consider off-label meds for refractory urticaria

The article has points that contribute to the differential diagnosis of Adult-onset Still's disease (AOSD).

Comment on the scientific letter "adult-onset still's disease mimicking acute rheumatic fever"/"Akut romatizmal ates'i taklit eden eriskin still hastaligi" baslikli bilimsel mektup hakkinda gorusler

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.

Hemophagocytic lymphohistiocytosis secondary to rheumatoid arthritis

Adult-onset Still's disease (AOSD) is an inflammatory disorder of unknown cause.

Application of fluorine-18-deoxyglucose positron emission tomography and gallium scan for assessment in a patient with adult-onset still's disease

Adult-onset Still's disease (AOSD) is a rare systemic inflammatory disease with unknown origin and pathogenesis.

Adult-onset still's disease mimicking acute rheumatic fever/Akut romatizmal ates'i taklit eden eriskin still hastaligi