Results 251 to 260 of about 4,968 (303)
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The American Journal of Medicine, 1980
The clinical and laboratory features in six patients with adult Still's disease are presented and compared with those in 52 other cases gathered from the literature. Although there is no pathognomonic abnormality, the condition can be readily recognized by the striking constellation of clinical and laboratory abnormalities.
J M, Esdaile, H, Tannenbaum, D, Hawkins
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The clinical and laboratory features in six patients with adult Still's disease are presented and compared with those in 52 other cases gathered from the literature. Although there is no pathognomonic abnormality, the condition can be readily recognized by the striking constellation of clinical and laboratory abnormalities.
J M, Esdaile, H, Tannenbaum, D, Hawkins
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British Journal of Dermatology, 1994
Adult Still's disease (ASD) is a rare disorder of unknown aetiology, characterized by an evanescent, erythematous, maculopapular rash, fever, arthralgia, and a variety of systemic features. We report a case which illustrates the typical features of ASD, and manifests the hitherto unreported complication of diffuse cutaneous mucinosis.
W G, Phillips +3 more
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Adult Still's disease (ASD) is a rare disorder of unknown aetiology, characterized by an evanescent, erythematous, maculopapular rash, fever, arthralgia, and a variety of systemic features. We report a case which illustrates the typical features of ASD, and manifests the hitherto unreported complication of diffuse cutaneous mucinosis.
W G, Phillips +3 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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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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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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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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Nishi Nihon Hifuka, 2000
成人Still病の3例を報告した(症例1:29歳男性,症例2:37歳男性,症例3:33歳女性)。39℃ 以上の弛張熱,出没を繰り返す淡紅色斑,関節痛,咽頭痛を伴い,抗核抗体,リウマチ因子は陰性だった。3例中2例は白血球増多,正常上限4倍以上のフェリチン高値を認めた。症例2は心嚢水,胸水の貯留を伴っていた。3例とも,皮疹は,そう痒を伴わない示指頭大までの小紅斑で,発熱とともに四肢を中心に出没を繰り返した。組織学的に,真皮上層の浮腫,毛細血管拡張,血管周囲性および膠原線維間にリンパ球を中心にわずかに好中球を含む軽度の細胞浸潤を認めた。いずれもステロイド療法が有効であったが,症例1はパルス療法を要した。
Fumiko NAGATO +4 more
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成人Still病の3例を報告した(症例1:29歳男性,症例2:37歳男性,症例3:33歳女性)。39℃ 以上の弛張熱,出没を繰り返す淡紅色斑,関節痛,咽頭痛を伴い,抗核抗体,リウマチ因子は陰性だった。3例中2例は白血球増多,正常上限4倍以上のフェリチン高値を認めた。症例2は心嚢水,胸水の貯留を伴っていた。3例とも,皮疹は,そう痒を伴わない示指頭大までの小紅斑で,発熱とともに四肢を中心に出没を繰り返した。組織学的に,真皮上層の浮腫,毛細血管拡張,血管周囲性および膠原線維間にリンパ球を中心にわずかに好中球を含む軽度の細胞浸潤を認めた。いずれもステロイド療法が有効であったが,症例1はパルス療法を要した。
Fumiko NAGATO +4 more
openaire +1 more source