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Update on pediatric vasculitis.

机译:小儿血管炎的更新。

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PURPOSE OF REVIEW: The purpose of this review is to provide an overview of the recent research and progress made in the field of pediatric vasculitis. RECENT FINDINGS: Over the past year, researchers have described several polymorphisms in Henoch-Schonlein purpura and Kawasaki Disease as well as the association between various vasculitides and infections. International and multidisciplinary efforts in Kawasaki Disease have resulted in recommendations for its diagnosis, treatment, and long-term management to improve patient care and further increase global collaboration. Researchers are investigating the role of inflammation and its role in endothelial health and atherosclerosis. Treatment regimens continue to improve, with the use of different immunosuppressive medications; however, we continue to have incomplete treatment successes. SUMMARY: Vasculitides are rare conditions with significant morbidity and mortality whose prognosis has improved with newer diagnostic modalities and treatments; however, we continue to have insufficient knowledge of vasculitides and lack unambiguous diagnostic criteria. As technology continues to progress it is clear that a single cause of these diseases may be an oversimplification: the genetic makeup of individuals, as well as various environmental exposures, are of vital importance in the pathophysiology and evolution of disease processes, as well as response to therapy. Efforts should continue to improve international multicenter collaboration and interdisciplinary efforts to help solve this ever-growing puzzle.
机译:审查的目的:这次审查的目的是概述在小儿血管炎领域的最新研究和进展。最近的发现:在过去的一年中,研究人员描述了过敏性紫癜和川崎病的几种多态性,以及各种脉管炎和感染之间的关系。川崎病的国际和多学科研究为诊断,治疗和长期管理提出了建议,以改善患者护理并进一步加强全球合作。研究人员正在研究炎症的作用及其在内皮健康和动脉粥样硬化中的作用。通过使用不同的免疫抑制药物,治疗方案继续得到改善。但是,我们仍然无法获得完全的治疗成功。摘要:血管肽是一种罕见的疾病,其发病率和死亡率很高,通过更新的诊断方法和治疗可以改善预后。但是,我们仍然对血管肽缺乏了解,缺乏明确的诊断标准。随着技术的不断进步,很明显,这些疾病的单一原因可能是过分简单化的:个体的遗传构成以及各种环境暴露对于疾病过程的病理生理学和演变以及反应至关重要。治疗。应继续努力改善国际多中心合作和跨学科工作,以帮助解决这一日益增长的难题。

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