Results 211 to 220 of about 3,081 (242)
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Myocarditis in adult Still's disease
International Journal of Cardiology, 1990An original case study of a myocardial involvement in a patient with adult Still's disease is presented. The fibrinoid necrosis appearance of a myocardial vessel is an unusual finding at histology.
R N, Sachs, O, Talvard, J, Lanfranchi
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Clinical Rheumatology, 1989
Three patients with adult onset of Still's disease are presented. Common early findings were: septic fever, polyarthralgia, leukocytosis, neutrophilia and elevated sedimentation rate. All of them had abnormal liver function tests which returned to normal values following corticosteroid therapy.
N, Arber +4 more
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Three patients with adult onset of Still's disease are presented. Common early findings were: septic fever, polyarthralgia, leukocytosis, neutrophilia and elevated sedimentation rate. All of them had abnormal liver function tests which returned to normal values following corticosteroid therapy.
N, Arber +4 more
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Best Practice & Research Clinical Rheumatology, 2004
Adult-onset Still's disease (AOSD) is a systemic inflammatory disorder of unknown etiology and pathogenesis. AOSD is a rare condition, usually presenting with high fever accompanied by systemic manifestations. The disease is a heterogeneous pathological entity with a range of etiologies, manifestations and prognosis.
János, Kádár, Edina, Petrovicz
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Adult-onset Still's disease (AOSD) is a systemic inflammatory disorder of unknown etiology and pathogenesis. AOSD is a rare condition, usually presenting with high fever accompanied by systemic manifestations. The disease is a heterogeneous pathological entity with a range of etiologies, manifestations and prognosis.
János, Kádár, Edina, Petrovicz
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Baillière's Clinical Rheumatology, 1991
Adult onset Still's disease seems to be the adult form of Still's disease in children. The key symptoms of the disease are high spiking fever, arthritis and a macular or maculopapular, salmon-pink evanescent rash, almost always accompanied by neutrophilic leukocytosis and frequently by sore throat, intense myalgias, lymphadenopathy, splenomegaly and ...
L B, van de Putte, J M, Wouters
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Adult onset Still's disease seems to be the adult form of Still's disease in children. The key symptoms of the disease are high spiking fever, arthritis and a macular or maculopapular, salmon-pink evanescent rash, almost always accompanied by neutrophilic leukocytosis and frequently by sore throat, intense myalgias, lymphadenopathy, splenomegaly and ...
L B, van de Putte, J M, Wouters
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Medicina Clínica (English Edition), 2018
Adult onset Still's disease is a rare systemic condition at the crossroads between auto-inflammatory syndromes and autoimmune diseases, with considerable heterogeneity in terms of clinical presentation, evolution and severity. This article reviews the main advances and lesser known aspects of this entity related to its clinical spectrum (atypical ...
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Adult onset Still's disease is a rare systemic condition at the crossroads between auto-inflammatory syndromes and autoimmune diseases, with considerable heterogeneity in terms of clinical presentation, evolution and severity. This article reviews the main advances and lesser known aspects of this entity related to its clinical spectrum (atypical ...
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[Still's disease in the adult].
Recenti progressi in medicina, 1994The adult Still's disease (ASD) is an uncommon inflammatory systemic disorder which affects the young adult. It is characterized by high spiking fever, vanishing rash, oligopolyarthritis, neutrophilic leucocytosis, negative titers for rheumatoid factor and antinuclear antibodies.
MITTERHOFER, Anna Paola, BONOMO L.
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Best Practice & Research Clinical Rheumatology, 2008
Adult-onset Still disease (AOSD) is an uncommon inflammatory condition of unknown origin typically characterized by four main (cardinal) symptoms: spiking fever > or =39 degrees C, arthralgia or arthritis, skin rash and hyperleucocytosis (> or =10,000 cells/mm3) with neutrophils > or =80%.
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Adult-onset Still disease (AOSD) is an uncommon inflammatory condition of unknown origin typically characterized by four main (cardinal) symptoms: spiking fever > or =39 degrees C, arthralgia or arthritis, skin rash and hyperleucocytosis (> or =10,000 cells/mm3) with neutrophils > or =80%.
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2021
Fever, rash, and arthritis constitute the characteristic triad of Adult Still’s disease which is considered the adult counterpart of systemic-onset JIA (juvenile idiopathic arthritis). There are no definitive laboratory markers or imaging findings.
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Fever, rash, and arthritis constitute the characteristic triad of Adult Still’s disease which is considered the adult counterpart of systemic-onset JIA (juvenile idiopathic arthritis). There are no definitive laboratory markers or imaging findings.
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2008
Adult Still disease (ASD) is a rare systemic inflammatory disorder of unknown etiology chracterized by spiking fever with evanescent rash, arthritis, arthralgia and multiorgan involvenent. It often poses a diagnostic and therapeutic challenge however clear clinical guidelines are lacking.
Alon Eisen, Howard Amital
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Adult Still disease (ASD) is a rare systemic inflammatory disorder of unknown etiology chracterized by spiking fever with evanescent rash, arthritis, arthralgia and multiorgan involvenent. It often poses a diagnostic and therapeutic challenge however clear clinical guidelines are lacking.
Alon Eisen, Howard Amital
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[Still's disease in the adult].
Revue medicale de Liege, 2002The Adult Onset Still's Disease (AOSD) is an entity of unknown origin characterised by fever, polyarthralgias or polyarthritis, a pharyngitis, a cutaneous eruption and elevation of leucocytes. We present observations of 17 patients diagnosed during the last thirteen years.
D, Nkoghe +5 more
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