Results 261 to 270 of about 4,968 (303)
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2021
Fever, rash, and arthritis constitute the characteristic triad of Adult Still’s disease which is considered the adult counterpart of systemic-onset JIA (juvenile idiopathic arthritis). There are no definitive laboratory markers or imaging findings.
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Fever, rash, and arthritis constitute the characteristic triad of Adult Still’s disease which is considered the adult counterpart of systemic-onset JIA (juvenile idiopathic arthritis). There are no definitive laboratory markers or imaging findings.
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Myocarditis in adult Still's disease
International Journal of Cardiology, 1990An original case study of a myocardial involvement in a patient with adult Still's disease is presented. The fibrinoid necrosis appearance of a myocardial vessel is an unusual finding at histology.
R N, Sachs, O, Talvard, J, Lanfranchi
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Nihon rinsho. Japanese journal of clinical medicine, 1999
Adult onset Still's disease was first reported by Bywaters in 1971. It is a systemic inflammatory disorder of unknown etiology, characterized by spiking fever, macular rash and polyarthritis. Although the prognosis is generally good, severe cases have been published. They include those with disseminated intravascular coagulation (DIC), hemophagocytosis,
H, Nara, A, Mimori
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Adult onset Still's disease was first reported by Bywaters in 1971. It is a systemic inflammatory disorder of unknown etiology, characterized by spiking fever, macular rash and polyarthritis. Although the prognosis is generally good, severe cases have been published. They include those with disseminated intravascular coagulation (DIC), hemophagocytosis,
H, Nara, A, Mimori
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2008
Adult Still disease (ASD) is a rare systemic inflammatory disorder of unknown etiology chracterized by spiking fever with evanescent rash, arthritis, arthralgia and multiorgan involvenent. It often poses a diagnostic and therapeutic challenge however clear clinical guidelines are lacking.
Alon Eisen, Howard Amital
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Adult Still disease (ASD) is a rare systemic inflammatory disorder of unknown etiology chracterized by spiking fever with evanescent rash, arthritis, arthralgia and multiorgan involvenent. It often poses a diagnostic and therapeutic challenge however clear clinical guidelines are lacking.
Alon Eisen, Howard Amital
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Der adulte Morbus Still (Adult onset Still’s disease, AOSD)
2010Das Still-Syndrom des Erwachsenen ist eine seltene, hoch fieberhafte rheumatische Systemerkrankung unbekannter Atiologie und Pathogenese. In erster Linie sind junge Erwachsene zwischen dem 16. und 35. Lebensjahr betroffen. Charakteristisch ist die Trias aus hohem intermittierendem Fieber, einem lachsfarbenen Exanthem im Bereich des Stammes oder an den ...
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2020
Still's disease is a systemic rheumatic disease of childhood which may persist into adulthood or may occur de novo in the adult population. It is classically distinguished by high fever, rash, arthritis, sore throat. Other clinical features may include lymphadenopathy, hepatosplenomegaly, pleuritis and pericarditis.
Ulusoy H., Bilgici A., Kuru Ö.
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Still's disease is a systemic rheumatic disease of childhood which may persist into adulthood or may occur de novo in the adult population. It is classically distinguished by high fever, rash, arthritis, sore throat. Other clinical features may include lymphadenopathy, hepatosplenomegaly, pleuritis and pericarditis.
Ulusoy H., Bilgici A., Kuru Ö.
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Nihon rinsho. Japanese journal of clinical medicine, 1992
Still's disease was reported to be a type of Juvenile Rheumatoid Arthritis (JRA) by Still in 1897. Adult-onset Still's disease is an important clinical entity inducing fever, skin rash and polyarthritis. Spiking fever and rash are characteristic features for early diagnosis.
M, Hara, S, Kashiwazaki
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Still's disease was reported to be a type of Juvenile Rheumatoid Arthritis (JRA) by Still in 1897. Adult-onset Still's disease is an important clinical entity inducing fever, skin rash and polyarthritis. Spiking fever and rash are characteristic features for early diagnosis.
M, Hara, S, Kashiwazaki
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[Still's disease in the adult].
Recenti progressi in medicina, 1994The adult Still's disease (ASD) is an uncommon inflammatory systemic disorder which affects the young adult. It is characterized by high spiking fever, vanishing rash, oligopolyarthritis, neutrophilic leucocytosis, negative titers for rheumatoid factor and antinuclear antibodies.
MITTERHOFER, Anna Paola, BONOMO L.
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