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].
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.