Suppr超能文献

无脾症与系统性红斑狼疮。

Asplenism and systemic lupus erythematosus.

作者信息

Lioté F, Angle J, Gilmore N, Osterland C K

机构信息

Clinique de Rhumatologie (Centre Viggo Petersen), Hôpital Lariboisière, Paris, France.

出版信息

Clin Rheumatol. 1995 Mar;14(2):220-3. doi: 10.1007/BF02214949.

Abstract

Although functional hyposplenism, secondary to Fc-receptor blockage by circulating immune complexes saturation, has been described in systemic lupus erythematosus (SLE), only few cases of complete asplenism have been reported. We observed a 60-year-old woman with congenital asplenism who presented with active SLE. The course and the clinical characteristics of such patients are reviewed and the relationship between the asplenic state and initiation and severity of SLE are discussed. These patients are at high risk for fatal pneumococcemia and pneumococcal vaccine is recommended even if long term results are still conflicting.

摘要

尽管在系统性红斑狼疮(SLE)中已描述过因循环免疫复合物饱和导致Fc受体阻滞继发的功能性脾功能减退,但仅有少数完全无脾的病例报道。我们观察到一名60岁先天性无脾的女性患者出现了活动性SLE。本文回顾了此类患者的病程及临床特征,并讨论了无脾状态与SLE发病及严重程度之间的关系。这些患者发生致命性肺炎球菌血症的风险很高,即使长期结果仍存在争议,仍建议接种肺炎球菌疫苗。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验