Adult-onset Still's disease [PDF]
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
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Non-Hodgkin's lymphoma in a woman with adult-onset Still's disease: a case report [PDF]
Journal of Medical Case Reports, 2008 Introduction Adult onset Still's disease is a chronic multisystemic inflammatory disorder characterized by high spiking fever, polyarthralgia and rash.
Otrock Zaher K +5 more
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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
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Adult Onset Still's Disease and Rocky Mountain Spotted Fever [PDF]
Case Reports in Medicine, 2010 Adult Still's Disease was first described in 1971 by Bywaters in fourteen adult female patients who presented with symptoms indistinguishable from that of classic childhood Still's Disease (Bywaters, 1971).
Paul Persad +2 more
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The cause of fever and pulmonary infiltrate: a difficult etiological diagnosis [PDF]
Emergency Care Journal, 2017 Adult-onset Still’s disease is a rare condition that typically presents itself with intermittent fever, arthralgia and salmon colored rash. The involvement of the in lung is less common and very rare.
Bahjat Barakat, Raffaele Pezzilli
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Difficulties in diagnosis and treatment of adult-onset Still's disease concurrent with pericardial effusion as a leading clinical manifestation [PDF]
Современная ревматология, 2016 The paper considers a case of adult-onset Still's disease that occurred as acute pericarditis, two-spike hectic fever, and neutrophilic leukocytosis in a young man.
V. Yu. Myachikova +5 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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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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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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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
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