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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Another novel presentation involves a heterozygous mutation of the LPIN2 gene manifesting as adult-onset Still's disease (SoJIA).

Novel presentations of periodic fever syndromes: Discrepancies between genetic and clinical diagnoses

[5.] Adult-onset Still's disease: an unusual presentation of rubella infection.Huang SH, DeCoteau WE Can Med Assoc J.

Adult Onset Still's Disease: A Case Report

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].

A Case of Spontaneously Improving Secondary Hemophagocytic Lymphohistiocytosis in an Adult Associated with T-Cell Histiocyte-Rich Large B-Cell Lymphoma

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].

Efficacy of Cyclosporine in the Induction and Maintenance of Remission in a Systemic Lupus Erythematosus Patient Presenting with Macrophage-Activating Syndrome

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

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.

Kumail Nanjiani on how to shut down 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

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].

Diagnostic Challenge: A Report of Two Adult-Onset Still's Disease Cases

Persistent pruritic papules and plaques associated with adult-onset Still's disease: report of six cases.

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