Results 1 to 10 of about 2,676 (234)
Научно-практическая ревматология, 2011 Adult-onset Still's disease is a rare inflammatory systemic disease. Cardinal symptoms/manifestations are fever, arthralgias or arthritis, myalgias, the typical skin rash, sore throat, hepatosplenomegaly, lymphadenopathy and serositis. Several other symptoms and organ involvements are possible.
Yu V Murav'ev +3 more
doaj +5 more sources
Septic arthritis or adult-onset still’s disease: analyzing the causes of recurrent fever after arthroscopic combined anterior cruciate ligament and posterior cruciate ligament reconstruction: a case report [PDF]
BMC Musculoskeletal DisordersBackground Adult-onset still’s disease and septic arthritis share similar symptoms—fever, joint pain, and limited mobility—making postoperative diagnosis difficult after combined anterior cruciate ligament and posterior cruciate ligament reconstruction ...
Zenan Tian +11 more
doaj +2 more sources
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
doaj +2 more sources
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
doaj +1 more source
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
doaj +1 more source
Adult Onset Still’s Disease [PDF]
Journal of Evolution of Medical and Dental Sciences, 2019 Adult-onset Still’s disease (AoSD) is a rare but clinically well-known, polygenic, systemic autoinflammatory disease. It is typically characterized by four main (cardinal) symptoms: spiking fever ≥39 °C, arthralgia or arthritis, skin rash, and hyperleukocytosis (≥10,000 cells/mm(3)). However, many other clinical features are possible, and it can appear
Bimal K. Agrawal +2 more
+5 more sources
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
doaj +1 more source
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
doaj +1 more source
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
openaire +4 more sources
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
doaj +1 more source