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
doaj +7 more sources
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
doaj +5 more sources
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
doaj +4 more sources
Adult‐onset Still's disease complicated by macrophage activation syndrome [PDF]
Clinical Case Reports, 2023 Key Clinical Message Young patients with persistent rash and fevers despite antibiotic treatment should be evaluated for non‐infectious etiologies. In our patient's case, these findings led to a diagnosis of MAS, which ultimately affected how she was ...
Toluwalase Awoyemi +2 more
doaj +2 more sources
Cryoglobulinemia vasculitis associated with adult‐onset Still's disease [PDF]
Clinical Case ReportsKey Clinical Message The present case indicates that cryoglobulinemia vasculitis should be considered in the differential diagnosis of purpura in patients with adult‐onset Still's disease (AOSD).
Noriharu Nakagawa +3 more
doaj +2 more sources
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
doaj +4 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
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
doaj +3 more sources
Coincidence or association: Adult‐onset Still's disease following HPV vaccine [PDF]
Clinical Case ReportsKey Clinical Message This case details adult‐onset Still's disease (AOSD) onset post‐human papillomavirus (HPV) vaccination and acute gastroenteritis. The timing of HPV vaccine and vaccine‐autoimmune disease literature may potentially confound the well ...
Muhammad Ahmed +5 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