冯莉霞, 朱剑, 张江林. 系统性红斑狼疮合并肺出血临床分析[J]. 解放军医学院学报, 2015, 36(11): 1068-1070,1074. DOI: 10.3969/j.issn.2095-5227.2015.11.002
引用本文: 冯莉霞, 朱剑, 张江林. 系统性红斑狼疮合并肺出血临床分析[J]. 解放军医学院学报, 2015, 36(11): 1068-1070,1074. DOI: 10.3969/j.issn.2095-5227.2015.11.002
FENG Lixia, ZHU Jian, ZHANG Jianglin. Analysis of systemic lupus erythematosus patients complicated with diffuse alveolar hemorrhage[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2015, 36(11): 1068-1070,1074. DOI: 10.3969/j.issn.2095-5227.2015.11.002
Citation: FENG Lixia, ZHU Jian, ZHANG Jianglin. Analysis of systemic lupus erythematosus patients complicated with diffuse alveolar hemorrhage[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2015, 36(11): 1068-1070,1074. DOI: 10.3969/j.issn.2095-5227.2015.11.002

系统性红斑狼疮合并肺出血临床分析

Analysis of systemic lupus erythematosus patients complicated with diffuse alveolar hemorrhage

  • 摘要: 目的 分析系统性红斑狼疮(systemic lupus erythematosus,SLE)合并肺出血患者的临床特点,提高对该病的认识。 方法 收集本院风湿科2008年12月- 2015年3月收治的SLE合并肺出血患者的临床资料,分析其病例特点并进行文献复习。 结果 共收集8例患者,男性2例,女性6例,平均年龄34(15 ~ 56)岁,平均病程30(2 ~ 96)个月。临床均表现为咯血或痰中带血、低氧血症、贫血和肺部弥漫性浸润影。8例中,肾损害6例,血液系统受累4例,肺间质病变2例,肺动脉高压1例,均无中枢神经系统受累,平均SLEDAI积分为6.6分。患者均接受了大剂量激素冲击治疗和人免疫球蛋白治疗,接受免疫抑制剂治疗5例。3例治疗无效死亡。 结论 肺出血是SLE较少见并发症,可发生于疾病的任何阶段,预后较差。

     

    Abstract: Objective To analyze the clinical features of systemic lupus erythematosus (SLE) patients complicated with diffuse alveolar hemorrhage (DAH). Methods Clinical data about SLE patients complicated with DAH admitted to the department of rheumatology in our hospital from December 2008 to March 2015 were retrospectively analyzed and its related literatures were reviewed. Results The average age of the 8 SLE patients (2 males and 6 females) complicated with pulmonary hemorrhage included in this study was 34 years. And the mean course of disease was 30 months. All these patients presented with hemoptysis, blood in sputum, hypoxemia, anemia, and new infiltrates on chest CT scan. There were 6 cases with lupus nephritis, 4 with leukopenia or thrombocytopenia, 2 with pulmonary interstitial fibrosis, 1 with pulmonary hypertension and no lupus encephalopathy was found. The mean systemic lupus erythematosus disease activity index (SLEDAI) was 6.6. All patients received steroid pulse therapy together with intravenous immunoglobulin, and 5 of them received immunosuppressor. Three patients died. Conclusion DAH is a rare and catastrophic event in SLE. DAH can occur at any stage of the disease course. Early aggressive management with high-dose steroids may improve the prognosis of DAH.

     

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