Adult-onset Still's disease (AOSD) is a systemic inflammatory disorder of unknown etiology
usually affecting young adults; spiking fever, arthritis and evanescent rash are commonly …

First described in 1971, adult-onset Still's disease (AOSD) is a rare multisystemic disorder
considered as a complex (multigenic) autoinflammatory syndrome. A genetic background …

Background: Adult onset Still's disease (AOSD) is a rare systemic inflammatory disorder of
unknown aetiology that is responsible for a significant proportion of cases of fever of …

Collapsing glomerulopathy represents a special variant of the proteinuric kidney disease
focal segmental glomerulosclerosis (FSGS). Histologically, the collapsing form of FSGS …

Adult-onset Still's disease (AOSD) is a rare systemic inflammatory disorder mainly
characterized by persistent high spiking fevers, evanescent rash, and joint involvement. The …

Collapsing glomerulopathy (CG) has become an important cause of ESRD. First delineated
from other proteinuric glomerular lesions in the 1980s, CG is now recognized as a common …

Adult-onset Still's disease (AOSD) is a rare, systemic inflammatory disease of unknown
aetiology, characterized by daily high spiking fevers, evanescent rash and arthritis. Our …

OBJECTIVE: To review recent literature regarding the pathogenesis and treatment of adult-
onset Still's disease (AOSD). METHODS: We searched MEDLINE and PUBMED from 1971 …

Abstract Objective Adult-onset Still's disease (AOSD) is a rare inflammatory disease that may
be life-threatening if complicated by cardiac problems. We performed a retrospective …

Aims Refractory recurrent pericarditis is a major clinical challenge after colchicine failure,
especially in corticosteroid-dependent patients. Human intravenous immunoglobulins …