文献资料 > 变应性亚败血症
Adult-onset Still’s Disease Complicated With Hemophagocytic Syndrome2014.02.28
Abstract: Hemophagocytic syndrome (HS) that occurs in the course of adult-onset Still’s disease (AOSD) has been reported only rarely in the literature. HS and AOSD share overlapping clinical and laboratory features, therefore, it is difficult to rec...
A case of Crohn's disease complicated by Adult Onset Still's Disease2014.02.28
AbstractArthritis and arthralgia are the most common extra-intestinal manifestations of Inflammatory Bowel Disease (IBD), occurring in up to a third of patients. These may affect the peripheral or axial skeletal system and may or may not reflect dise...
A case of adult-onset Still’s disease complicated by hemophagocytic syndrome and interstitial pneumonia with pneumomediastinum/recurrent pneumothorax2014.02.28
Abstract:We report, to our knowledge, the first case of adult-onset Still’s disease (AOSD) complicated by hemophagocytic syndrome (HPS) and interstitial pneumonia (IP) with pneumomediastinum and recurrent pneumothorax. A 64-year-old Japanese woman ...
Adult-onset Still’s disease with dermatomyositis-like eruption2014.02.28
Abstract:Adult-onset Still’s disease (AOSD) is an inflammatory disorder of unknown etiology and its characteristic symptoms are spiking fever, polyarthralgia, and salmon-pink evanescent rash on the trunk and proximal extremities.1 However, there ar...
A case of adult-onset Still’s disease complicated with atypical pulmonary defect2014.02.28
成人Still病并发非典型肺缺陷一例
Adult-onset Still’sdisease (AOSD) is an uncommon inflammatorycondition of unknown origin and pathogenesis. Pulmonary involvement is rare andincludes pleural effusionand transient pulmonary infiltrates.We describe and discuss difficulties in the di...
Biological treatment in adult-onset Still’s disease2014.02.28
Abstract:Adult-onset Still’s disease (AOSD) is a rare systemic inflammatory disorder that is characterised by high spiking fever, arthritis or arthralgia, and evanescent rash.Many other systemic manifestations may occur. Pathogenesis of AOSD remains...
Adult-onset Still’s disease with macrophage activation syndrome successfully treated with a combination of methotrexate and etanercept2014.02.28
Abstract We report a 16-year-old female case of intractable adult-onset Still’s disease accompanied by macrophage activation syndrome, who went into full remission after switching from infliximab to etanercept. Although the disease promptly relapsed...
Adult-onset Still’s disease in a patient with cystic fibrosis and its successful treatment with anakinra2014.02.28
Abstract: We report the case of a 22-year-old woman with a known history of cystic fibrosis. She initially reported subfebrile temperatures with an increase in her fever up to 40C in recent days, a sore throat and a macular rash on both forearms fo...
Tocilizumab in the treatment of the adult-onset Still's disease: current clinical evidence2014.02.28
Abstract This study aimed to review and analyze the effectiveness and safety of tocilizumab in the treatment of patients with adult-onset Still's disease (AOSD). We report on two patients with AOSD who were successfully treated with tocilizumab. ...
The Use of Canakinumab, a Novel IL-1 Long-Acting Inhibitor, in Refractory Adult-Onset Still’s Disease2014.02.28
采用康纳单抗,一种新型IL-1β长效抑制剂治疗难治性成人Still病
目标:We describe the successful treatment of adult-onset Still’s disease (AOSD)with canakinumab, a novel anti-interleukin (IL)-1β ,long-acting, monoclonal antibody, on patients refractory to anakinra andrilonacept. In many cases the expected posit...
The associations of circulating CD4+CD25high regulatory T cells and TGF-b with disease activity and clinical course in patients with adult-onset Still’s disease2014.02.27
ABSTRACT ObjectiveTo determine circulating levels of CD4+CD25high regulatory T (Treg) cells and transforming growth factor-β (TGF-β) in patients with adult-onset Still’s disease (AOSD) and to examine the associations with disease activity and clin...
Neutrophil CD64 is upregulated in patients with active adult-onset Still’s disease2014.02.27
Abstract:CD64 (Fc gamma-receptor I, FcγRI), one of the Fc receptors for immunoglobulin (Ig)G, is constitutively expressed on macrophages and monocytes, and is upregulated on neutrophils as part of the systemic response to infection . Studies have sh...
Correlation of serum CX3CL1 level with disease activity in adult-onset Still's disease and significant involvement in hemophagocytic syndrome2014.02.27
Abstract To investigate the characteristics of patients with adult-onset Still's disease (AOSD), serum cytokines and chemokines were measured to examine their associations with systemic manifestations of AOSD, especially hemophagocytic syndrome (...
Coexistence of adult-onset Still’s disease and autoimmune hyperthyroidism in a patient who responded to corticosteroids and β-blocker2014.02.27
AbstractThe pathogenesis of adult-onset Still’s disease (AOSD), which is currently thought to be an autoimmune disorder, may share similarities with autoimmune hyperthyroidism. This report describes a middle-aged woman in whom hyperthyroidism and St...
Germinal center kinase-like kinase (GLK/MAP4K3) expression is increased in adult-onset Still’s disease and may act as an activity marker2014.02.27
成人Still病中生发中心激酶样激酶(GLK/MAP4K3 )表达增加并可能作为一个活动标记
Background: 背景: Germinal center kinase-like kinase (GLK, alsotermed MAP4K3), a member of the MAP4K family, may regulate gene transcription,apoptosis and immune inflammation in response to extracellular signals. Theenhanced expression of GLK has b...
共有20条记录  当前第1页  首页 上一页 下一页 尾页