Suppr超能文献

墨西哥“rhupus”患者的临床与免疫遗传学特征

Clinical and immunogenetic characterization of Mexican patients with 'rhupus'.

作者信息

Simón J A, Granados J, Cabiedes J, Morales J Ruíz, Varela J Alcocer

机构信息

Department of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Tlalpan, CP, México DF.

出版信息

Lupus. 2002;11(5):287-92. doi: 10.1191/0961203302lu189oa.

Abstract

The coexistence of systemic lupus erythematosus and rheumatoid arthritis (rhupus), is a rare clinical condition. To date, 50 cases of rhupus have been described worldwide; however, the lack of clinical criteria for this rheumatic condition has created confusion in the characterization of this disorder. Nevertheless, in this paper we describe a comprehensive clinical and serological characterization of a cohort of 22 Mexican patients with rhupus, supported by generic HLA-DR phenotyping. We found that rhupus patients have a special clinical behavior. In this setting, the signs and symptoms of rheumatoid arthritis prevail, little organic damage associated with systemic lupus erythematosus (SLE) exists and none of the cases present thrombosis or morbidity during pregnancy in spite of presenting a high frequency of anticardiolipin antibodies. We also found an increased frequency of HLA-DR1 and HLA-DR2 alleles compared to healthy ethnically matched controls, systemic lupus erythematosus and rheumatoid arthritis patients.

摘要

系统性红斑狼疮与类风湿关节炎并存(rhupus)是一种罕见的临床病症。迄今为止,全球已报道了50例rhupus病例;然而,这种风湿性疾病缺乏临床标准,导致对该病症的特征描述存在混乱。尽管如此,在本文中,我们描述了一组22例墨西哥rhupus患者的全面临床和血清学特征,并通过通用的HLA - DR表型分析提供支持。我们发现rhupus患者具有特殊的临床行为。在这种情况下,类风湿关节炎的体征和症状占主导,与系统性红斑狼疮(SLE)相关的器质性损害较少,尽管抗心磷脂抗体频率较高,但所有病例在孕期均未出现血栓形成或发病情况。我们还发现,与种族匹配的健康对照、系统性红斑狼疮患者和类风湿关节炎患者相比,HLA - DR1和HLA - DR2等位基因的频率有所增加。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验