论文部分内容阅读
系统性红斑狼疮(SLE)是一种侵犯全身结缔组织的自身免疫性疾病,临床表现复杂多样,常为多脏器损害,病程迁延反复,缓解与复发交替出现。为提高对本病的认识和防治水平,现总结我院62~83年间住院的 SLE100例,其中资料完整符合全国统一诊断标准者75例作一分析。一般资料一、诊断标准全部病例符合以下三项诊断标准之一:1.有皮肤病变,又合并内脏损害,且狼疮(LE)细胞检查阳性或皮肤活检阳性者。2.虽无皮肤病变,但有多脏器损害,且 LE 细胞检查阳性者。3.有多脏器损害,基本符合美国风湿病学会诊断
Systemic lupus erythematosus (SLE) is an autoimmune disease that invades systemic connective tissue. Its clinical manifestations are complex and diverse. It is often impaired by multiple organs. The course of the disease is prolonged, and the relapse between remission and recurrence occurs alternately. In order to improve the understanding of the disease and prevention and treatment, we conclude 100 cases of hospitalized SLE in our hospital from 62 to 83 years, of which 75 cases with complete data in line with the national unified diagnostic criteria are analyzed. General information First, the diagnostic criteria All cases meet one of the following three diagnostic criteria: 1. There are skin lesions, and combined with visceral damage, and lupus (LE) cell test positive or skin biopsy positive. 2. Although no skin lesions, but there are multiple organ damage, and LE cells check positive. 3. Multiple organ damage, basically in line with the American College of Rheumatology diagnosis