Results 11 to 20 of about 2,775 (238)
Oral mucosa lesions as atypical manifestation of adult-onset Still´s disease [PDF]
Anais Brasileiros de Dermatologia, 2018 : Adult-onset Still's disease is a systemic inflammatory disorder of unknown etiology, characterized by skin rash, spiking fever, arthralgias or arthritis, and leukocytosis. The typical skin rash is evanescent, salmon-pink, nonpruritic and maculopapular,
María Lorena Brance, Eldo Luis Neffen
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Rheumatology International, 2009 Adult-onset Still's disease (AOSD) is a rare systemic inflammatory disorder characterised by high spiking fever, an evanescent salmon pink rash and arthritis, frequently accompanied by sore throat, myalgias, lymphadenopathies, splenomegaly and neutrophilic leukocytosis.
Bagnari V +4 more
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Adult-onset Still’s Disease: A Case Report
Journal of Nepal Medical Association, 2023 Pyrexia of unknown origin refers to a fever of over 38.3°C on multiple occasions for at least three weeks without a known aetiology, even after a week of hospitalization.
Bikash Karki +4 more
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Elderly-onset adult Still’s disease
Rheumatology, 2021 Adult-onset Still’s disease is a rare inflammatory disorder usually affecting young adults. Elderly-onset Still’s disease (EOSD) is reported in some cases, commonly in Japan, the USA and Europe.
Anis Mzabi +7 more
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Adult-Onset Still Disease (AOSD) [PDF]
The Journal of the American Board of Family Medicine, 2010 Adult-onset Still disease (AOSD) is an uncommon clinical entity that predominantly affects young adults. One of the most common presentations of the disease is fever of unknown origin. Early diagnosis can be difficult because fever of unknown origin is more commonly seen with other conditions such as malignancy or infection.
Egambaram, Senthilvel +3 more
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The association between adult-onset Still’s disease and collapsing glomerulopathy: a case report
Journal of Medical Case Reports, 2022 Background Collapsing glomerulopathy, characterized by marked hypertrophy and hyperplasia of the podocytes with eventual collapse of the glomerular tuft, is an important cause of end-stage renal disease. Among the many causes of collapsing glomerulopathy,
Matas Orentas +3 more
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Therapy with canakinumab for adult-onset still's disease
Научно-практическая ревматология, 2019 Still's disease in children (systemic-onset juvenile idiopathic arthritis, SoJIA) and in adults (adult-onset Still's disease) are considered as non-familial systemic autoinflammatory diseases of unknown etiology driven by similar immunopathogenetic ...
E. L. Nasonov
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JRSM Open, 2020 Adult-onset Still’s disease is a rare inflammatory disorder characterised by fever, arthritis and rash. It can present in a number of ways and is associated in 5% of cases with parenchymal lung involvement.
Robert Perry +4 more
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Refractory Adult Onset Still’s Disease [PDF]
Cureus, 2017 It is often a challenge and a dilemma for clinicians encountering patients with pyrexia of unknown origin. Numerous tests performed to determine the underlying cause often give inconclusive results. We present a 52-year-old man with undulating fever for more than 10 months with persistent hyperferritinaemia, and negative immunological and serological ...
Sulaiman, Wahinuddin +4 more
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Autoimmunity Reviews, 2014 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 would confer susceptibility to the development of autoinflammatory reactions to environmental triggers.
Gerfaud-Valentin, Mathieu +3 more
openaire +5 more sources