Results 1 to 10 of about 3,600 (117)
Application of machine learning techniques to explore the occurrence of macrophage activation syndrome in Still’s disease: results from the GIRRCS AOSD Study Group and the AIDA Network Still’s Disease Registry [PDF]
Frontiers in ImmunologyObjectivesThis study aims to explore the application of machine learning techniques in assessing macrophage activation syndrome (MAS) in Still’s disease.MethodsA multicenter, observational, prospective study was conducted, including patients with Still’s
Piero Ruscitti +120 more
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Still’s disease: bridging the gap between guidelines and clinical practice [PDF]
Pediatric Rheumatology Online JournalThe recently published EULAR/PReS recommendations on Still’s disease provide a comprehensive framework for disease classification and management, yet certain aspects warrant further refinement.
Çisem Yıldız +2 more
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Adult-onset Still’s disease with dermatomyositis-like lesions [PDF]
European Journal of Case Reports in Internal MedicineStill’s disease is an inflammatory disorder of unknown origin, also known as juvenile idiopathic arthritis, that predominantly affects children, as it usually appears before the age of 16. However, there is another presentation known as adult-onset Still’
Inés Segovia Rodríguez +6 more
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Adult Still’s disease – a multidisciplinary disease [PDF]
Archives of the Balkan Medical Union, 2021 Introduction. Adult-onset Still’s disease is a rare systemic autoinflammatory disorder of unknown etiology, characterized by persistent fever, maculopapular skin rash, and arthritis or arthralgia.
Leonid I. DVORETSKY +6 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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RMD Open, 2023 Objective Still’s disease is more frequently observed in the paediatric context, but a delayed onset is not exceptional both in the adulthood and in the elderly.
Micol Frassi +75 more
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Macrophage activation syndrome complicating early course of adult-onset Still’s disease [PDF]
Srpski Arhiv za Celokupno Lekarstvo, 2021 Introduction. Adult-onset Still’s disease is a rare inflammatory disorder of unknown etiology. It can be complicated by macrophage activation syndrome, a potentially life-threatening condition. While macrophage activation syndrome and adult-onset Still’s
Božić Ksenija +2 more
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Frontiers in Medicine, 2022 ObjectiveInterleukin (IL)-1 inhibitors are largely employed in patients with Still’s disease; in cases with refractory arthritis, IL-6 inhibitors have shown to be effective on articular inflammatory involvement.
Antonio Vitale +31 more
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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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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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