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Autoimmune manifestations in patients with multiple myeloma and monoclonal gammopathy of undetermined significance

机译:多发性骨髓瘤和单克隆丙种球蛋白病患者自身免疫表现的意义尚未确定

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Background Multiple myeloma (MM) and its precursor, monoclonal gammopathy of undetermined significance (MGUS), have been linked with several autoimmune conditions in the medical literature. Yet, significance of these associations is not well understood. Methods Herein, we provide a comprehensive literature review on autoimmune disorders identified in patients with MM and MGUS. Most relevant papers were identified via searching the PubMed/Medline and EMBASE databases for articles published from inception until May 1, 2016. Findings Scientific literature on autoimmune conditions in patients with MM and MGUS consists of several case series and a multitude of case reports. Our analysis suggests an increased prevalence of autoimmune conditions in patients with MM and monoclonal gammopathy of undetermined significance (MGUS), including various autoimmune hematologic and rheumatologic conditions among other entities. Conversely, persons with various autoimmune conditions tend to have a higher prevalence of MGUS and MM than the general population. Conclusions Future research is required to explore further the link between MGUS/MM and autoimmune disorders. Inflammation in the setting of autoimmunity may serve as a trigger for MGUS and MM. In addition, a common genetic susceptibility for developing both an autoimmune disease and MM/MGUS might also exist. Autoimmune hematologic and rheumatologic diseases may pose important clinical problems for the MM patients. Therefore, a catalogue of these problems is important so that physicians are able to consider, identify and address them promptly. ☆ We certify that we do not have any affiliation with or financial involvement in any organization or entity with a direct financial interest in the subject matter or materials discussed in the manuscript (e.g., employment, consultancies, stock ownership, honoraria, and expert testimony). We do not have any commercial or proprietary interest in any drug, device, or equipment mentioned in the article below. No financial support was used for this work. No previously published figures or tables were used in this paper. We certify sufficient participation of each author in the conception, design, analysis, interpretation, writing, revising, and approval of the manuscript. — The Authors View Abstract ? 2016 The Authors. Published by Elsevier B.V. No articles found. Citing articles View article metrics Elsevier About ScienceDirect Remote access Shopping cart Contact and support Terms and conditions Privacy policy We use cookies to help provide and enhance our service and tailor content and ads. By continuing you agree to the use of cookies .Copyright ? 2018 Elsevier B.V. or its licensors or contributors. ScienceDirect ? is a registered trademark of Elsevier B.V. RELX Group.
机译:背景技术在医学文献中,多发性骨髓瘤(MM)及其前体,意义不明的单克隆丙种球蛋白病(MGUS)与几种自身免疫性疾病有关。然而,这些协会的意义还没有被很好地理解。方法在本文中,我们提供了有关在MM和MGUS患者中发现的自身免疫性疾病的综合文献综述。通过搜索PubMed / Medline和EMBASE数据库查找从开始到2016年5月1日发表的文章,确定了最相关的论文。研究结果有关MM和MGUS患者自身免疫状况的科学文献包括多个病例系列和大量病例报告。我们的分析表明,具有未定意义的MM和单克隆丙种球蛋白病(MGUS)的患者自身免疫病患病率增加,其中包括其他个体的各种自身免疫血液病和风湿病病况。相反,具有各种自身免疫性疾病的人比一般人群的MGUS和MM患病率更高。结论需要进一步研究以进一步探索MGUS / MM与自身免疫性疾病之间的联系。自身免疫环境中的炎症可能是MGUS和MM的诱因。另外,也可能存在发展自身免疫性疾病和MM / MGUS的常见遗传易感性。自身免疫性血液病和风湿病可能给MM患者带来重要的临床问题。因此,这些问题的目录很重要,这样医生才能迅速考虑,识别和解决它们。 ☆我们证明,我们与任何在手稿中讨论的主题或材料具有直接财务利益的组织或实体没有任何从属关系或财务关系,酬金和专家证词)。对于以下文章中提及的任何药物,设备或设备,我们没有任何商业或专有利益。这项工作没有资金支持。本文未使用以前发布的图形或表格。我们保证每位作者充分参与稿件的概念,设计,分析,解释,写作,修订和批准。 —作者查看摘要? 2016作者。 Elsevier B.V.发布。未找到文章。引用文章查看文章度量标准Elsevier关于ScienceDirect远程访问购物车联系和支持条款和条件隐私权政策我们使用cookie来帮助提供和增强我们的服务,并定制内容和广告。如果继续,您同意使用Cookies。版权所有? 2018 Elsevier B.V.或其许可人或贡献者。 ScienceDirect?是Elsevier B.V. RELX Group的注册商标。

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