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首页> 外文期刊>Current Rheumatology Reviews >Mixed Connective Tissue Disease (MCTD) and Undifferentiated Connective Tissue Disease (UCTD)
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Mixed Connective Tissue Disease (MCTD) and Undifferentiated Connective Tissue Disease (UCTD)

机译:混合性结缔组织病(MCTD)和未分化的结缔组织病(UCTD)

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摘要

In Mixed Connective Tissue Disease (MCTD), features of various connective tissue disorders such as systemic lupus erythematosus (SLE), systemic sclerosis (PSSc), dermatomyositis/polymyositis (DM/PM), and occasionally Sjogren's syndrome and rheumatoid arthritis (RA) can coexist and overlap. The picture is marked by the presence of high titer anti-U1 ribonucleoprotein (RNP) antibodies. Over the last 30 years since first described a lot of controversial studies have been published regarding the nature, the severity or the very existence of the condition. We review here the various aspects and the characteristics which make it a distinctive autoimmune condition. We discuss the new understanding of the prognosis of this connective tissue disorder. We give an update on the management of MCTD. Some aspects of the Undifferentiated Connective Tissue Disease (UCTD) are approached as a class apart.
机译:在混合性结缔组织病(MCTD)中,各种结缔组织疾病的特征(例如系统性红斑狼疮(SLE),系统性硬化症(PSSc),皮肌炎/多发性肌炎(DM / PM)以及偶发的干燥综合征和类风湿关节炎(RA)均可共存和重叠。该图片的特点是存在高滴度的抗U1核糖核蛋白(RNP)抗体。自从首次描述以来的最近30年中,已经发表了许多有关该疾病的性质,严重性或确实存在的争议性研究。我们在这里回顾了使其成为独特的自身免疫性疾病的各个方面和特征。我们讨论了这种结缔组织疾病预后的新认识。我们提供有关MCTD管理的最新信息。未分化的结缔组织病(UCTD)的某些方面分开讨论。

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