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作 者:马劲夫[1] 张秋林 陈东 刘勇谋[1] 黎檀实[3]
机构地区:[1]解放军305医院呼吸科,北京100017 [2]解放军305医院肾内科,北京100017 [3]解放军总医院急诊科,北京100853
出 处:《现代生物医学进展》2012年第29期5741-5745,5722,共6页Progress in Modern Biomedicine
基 金:国家自然科学基金项目(30873179)
摘 要:目的:探讨Goodpasture综合征的临床特征及诊治要点。方法:对13例Goodpasture综合征患者的临床表现、实验室检查、诊断与治疗等资料进行回顾性分析。结果:13例患者中,全部患者(100%)均有咯血,12例(92.3%)有镜下血尿,大多数患者咯血症状先于肾小球肾炎症状出现。10例(83.3%)抗GBM抗体阳性。12例接受完整治疗方案的患者,有效7例,有效率58.3%。无效死亡5例,平均生存期为(91±100.1)月。结论:Goodpasture综合征是一组病变进展迅速,预后凶险的自身免疫性疾病,显效组在确诊天数上与有效组与死亡组间的差别具有统计学意义(P均<0.05),改善疾病预后的关键是早发现、早诊断、早治疗。ABSTRACT Objective: To discuss the clinical characteristic, assistance inspection and points for the diagnosis and therapy. Methods: Retrospective analysis of the 13-case was made on the clinical manifestation of Goodpasture syndrome, laboratorial tests, diagnosis and treatment. Results: In this cohort, haemoptysis which usually happened before renal presentation occurred in all patients and microscopic hematuria occurred in 12 (92.3%) patients. Ten patients (83.3%) were anti-GBM body positive. Seven eases were effective in 12 patients who received treatments and the effective rate was 58.3%. Five patients died and the mean survival time was 91± 100.072 months. Conclusion: Goodpasture syndrome is a group of autoimmune diseases which progresses rapidly and has a bad prognosis. The obvious effect group has statistic difference in the diagnosed days with effect group and non-effect group (P both 〈0.05). The key to improve prognosis is early discovery, early diagnosis and early treatment. Key words: Goodpasture syndrome; Anti-glomerular basement membrane antibody; Pulmonary hemorrhage; Acute glomerulonephritis
关 键 词:GOODPASTURE综合征 抗肾小球基底膜抗体 肺出血 急性肾小球肾炎
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