系统性红斑狼疮并发类远达性视网膜病变3例分析  

An Analysis of 3 Cases of Systemic Lupus Erythematosus Complicated by Purtscher-like Retinopathy

作　　者：赵文玲 苏真珍[1] 刘萍 伍叶[3] 黄卓春[1] 张君龙[1] 蔡蓓[1] ZHAO Wenling;SU Zhenzhen;LIU Ping;WU Ye;HUANG Zhuochun;ZHANG Junlong;CAI Bei(Department of Laboratory Medicine,West China Hospital,Sichuan University,Chengdu 610041,China;Department of Laboratory Medicine,363 Hospital,Chengdu 610041,China;Department of Ophthalmology,West China Hospital,Sichuan University,Chengdu 610041,China)

机构地区：[1]四川大学华西医院实验医学科,四川成都610041 [2]成都三六三医院检验科,四川成都610041 [3]四川大学华西医院眼科,四川成都610041

出　　处：《标记免疫分析与临床》2024年第3期583-588,共6页Labeled Immunoassays and Clinical Medicine

基　　金：四川省科技厅重点研发项目(编号:2020YFS0124)。

摘　　要：系统性红斑狼疮(systemic lupus erythematosus,SLE)患者可出现多器官、多系统的受累,极少数患者会并发类远达性视网膜病变(Purtscher-like retinopathy,PLR),该病变的SLE患者视力预后较差,若未及时接受治疗,视力损害将很难恢复。因此,早期识别该类疾病,对患者的诊治具有重要意义。本研究收集整理了3例四川大学华西医院风湿免疫科病房住院诊断为SLE并发PLR的病例资料及临床特征,同时进行相关文献复习,旨在为临床工作提供一定参考。Patients with systemic lupus erythematosus(SLE)might suffer from involvements of multiple organs and systems.A very small subset of SLE patients could develop a condition known as Purtscher-like retinopathy(PLR),which is associated with a poor prognosis for vision.Without timely treatment,the impairment of vision can be irreversible.Therefore,the early identification of such conditions is crucial for the diagnosis and management of affected patients.This study collected and analyzed datasets and clinical characteristics of three inpatients diagnosed with SLE that were complicated by PLR at the Department of Rheumatology and Immunology in West China Hospital,Sichuan University.In addition,a systematic review of previous relevant literatures was conducted to provide references for the clinical practice.

关 键 词：系统性红斑狼疮 类远达性视网膜病变 文献复习 

分 类 号：R593.241[医药卫生—内科学]