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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
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
Recurring Lower Abdominal Pain and Fever as Initial Presentation of Adult Onset Still’s Disease in the Absence of Arthralgia and Other System Involvement [PDF]
, 2017 A 34 year-old Afro-Caribbean female presented with recurring episodes of fever and lower abdominal pain over a period of two months not improving despite courses of antibiotics for possible recurrent urinary tract infections.
Rajaiah, Nithyananda +2 more
core +7 more sources
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
doaj +1 more source
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
openaire +2 more sources
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
openaire +2 more sources