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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, E L Nasonov, Yu V Muravyev, E L Nasonov   +3 more
doaj   +7 more sources

Adult-onset Still’s disease

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, COLINA, Matteo, CIANCIO, GIovanni, GOVONI, Marcello, TROTTA, Francesco   +4 more
semanticscholar   +5 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, Hatoum Hassan A, Uthman Imad W, Taher Ali T, Saab Shahrazad, Shamseddine Ali I   +5 more
doaj   +2 more sources

Adult-onset Still's disease

Autoimmunity Reviews, 2014
First described in 1971, adult-onset Still's disease (AOSD) is a rare multisystemic disorder considered as a complex (multigenic) autoinflammatory syndrome. A genetic background would confer susceptibility to the development of autoinflammatory reactions to environmental triggers.
Gerfaud-Valentin, Mathieu, Jamilloux, Yvan, Iwaz, Jean, Sève, Pascal   +3 more
semanticscholar   +6 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, Rajendrakumar Patel, Niki Patel   +2 more
doaj   +2 more sources

Adult-onset Still's disease: Evaluation of prognostic tools and validation of the systemic score by analysis of 100 cases from three centers [PDF]

BMC Medicine, 2016
Background: Adult-onset Still's disease (AOSD) is rare inflammatory disease of unknown etiology that usually affects young adults. The more common clinical manifestations are spiking fevers, arthritis, evanescent rash, elevated liver enzymes ...
Berardicurti O., Carubbi F., Ciccia F., Cipriani P., Di Benedetto P., Giacomelli R., Guggino G., Iacono D., Liakouli V., Masedu F., Ruscitti P., Triolo G., Valenti M., Valentini G.   +13 more
core   +2 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, Alexandra Conti, Frank G. Aguilar   +2 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

Cryoglobulinemia vasculitis associated with adult‐onset Still's disease [PDF]

Clinical Case Reports
Key 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, Ai Fujii, Yoshimichi Ueda, Masahide Yamazaki   +3 more
doaj   +2 more sources

Adult-onset Still’s disease with dermatomyositis-like lesions [PDF]

European Journal of Case Reports in Internal Medicine
Still’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, Juan Vicente de la Sota, Alba Hernández Piriz, María Castillo Gutiérrez, Teresa López Bernal, Beatriz Aranegui Arteaga, Elena García Guijarro   +6 more
doaj   +2 more sources