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 ?
Another novel presentation involves a heterozygous mutation of the LPIN2 gene manifesting as adult-onset Still's disease (SoJIA).
[5.] Adult-onset Still's disease: an unusual presentation of rubella infection.Huang SH, DeCoteau WE Can Med Assoc J.
It is occasionally confused with adult-onset Still's disease owing to a similar symptomatology and similar "cytokine storm" phenomenon; however, differences in certain lab values and the absence of bone marrow findings distinguish these two conditions [9].
MAS has been reported in patients with various rheumatic diseases, such as systemic juvenile idiopathic arthritis (sJIA), adult-onset Still's disease, dermatomyositis, and systemic lupus erythematosus (SLE) [1].
She had been put into a medically induced coma after coming down with an extremely rare illness, adult-onset Still's disease.
She had been put into a medically induced coma after coming down with an extremely rare illness, adult-onset Still's disease. At the time, Nanjiani, a Pakistani-American, was hiding their relationship from his parents, who wanted him to enter into an arranged marriage.
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.
Adult-onset Still's disease (AOSD) is a rare systemic inflammatory condition with unknown etiology that is characterized by high spiking fever, arthritis, typically salmonpink maculopapular rash, leukocytosis with neutrophilia, and multiple organs' involvement [1].
In August 2016, the European Commission approved Ilaris for a license extension to also treat patients with Adult-Onset Still's Disease (AOSD).
Persistent pruritic papules and plaques associated with adult-onset Still's disease: report of six cases.
Adult-onset Still's disease (AOSD) is a systemic inflammatory disorder characterized by high fever, arthralgia, transient rash, hepatosplenomegaly, lymphadenopathy, liver dysfunction, and leukocytosis.

Full browser ?