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发生严重血液学问题的系统性红斑狼疮患者的患病率、疾病模式及预后

Prevalence, patterns of disease and outcome in patients with systemic lupus erythematosus who develop severe haematological problems.

作者信息

Sultan S M, Begum S, Isenberg D A

机构信息

Centre for Rheumatology, Department of Medicine, University College Hospital, London W1P 9PG, UK.

出版信息

Rheumatology (Oxford). 2003 Feb;42(2):230-4. doi: 10.1093/rheumatology/keg069.

Abstract

OBJECTIVE

To evaluate the prevalence of major haemolytic disease-severe autoimmune haemolytic anaemia and severe thrombocytopenia-and to assess when these features develop. We also sought to analyse the clinical and serological outcomes of patients with haemolytic anaemia and thrombocytopenia with systemic lupus erythematosus (SLE) as compared with patients without these cytopenias.

METHODS

We reviewed retrospectively all the available case notes from our lupus cohort of 305 patients followed up between 1978 and 2000 (mean follow-up 7 yr). We identified 30 patients with SLE (9.8%), of whom 20 (6.6%) had severe haemolytic anaemia and 10 (3.3%) had severe thrombocytopenia. Each patient was matched for age, sex and ethnicity with two control patients.

RESULTS

We recorded a total of 42 episodes of severe haematological events: four patients had a second haemolytic episode and eight patients had a second thrombocytopenic episode. Five patients had both thrombocytopenia and haemolytic anaemia. One per cent of patients had severe haemolytic anaemia prior to the diagnosis of SLE and 2.5% of patients presented with these haematological disorders. Haemolytic anaemia and thrombocytopenia were associated with renal involvement (0.01>P>0.001) and anticardiolipin antibodies (ACL) (0.01>P>0.001), but not anti-dsDNA antibodies. Calculation of the BILAG index at the time of severe haematological crisis demonstrated that renal, central nervous system involvement and general symptoms are more frequently present. Forty-one per cent of patients were already on either prednisolone (<10 mg) or an immunosuppressive agent at the onset of the event.

CONCLUSION

Our data demonstrate that both haemolytic anaemia and thrombocytopenia are associated with ACL but not anti-dsDNA antibodies. When faced with a patient with a severe haematological manifestation of lupus, active disease in other organs is likely to be present.

摘要

目的

评估主要溶血性疾病——严重自身免疫性溶血性贫血和严重血小板减少症——的患病率,并评估这些特征何时出现。我们还试图分析与无这些血细胞减少症的患者相比,患有溶血性贫血和血小板减少症的系统性红斑狼疮(SLE)患者的临床和血清学结果。

方法

我们回顾性分析了1978年至2000年随访的305例狼疮队列患者的所有可用病历(平均随访7年)。我们确定了30例SLE患者(9.8%),其中20例(6.6%)患有严重溶血性贫血,10例(3.3%)患有严重血小板减少症。为每位患者匹配年龄、性别和种族的两名对照患者。

结果

我们共记录了42次严重血液学事件:4例患者发生第二次溶血性发作,8例患者发生第二次血小板减少发作。5例患者同时患有血小板减少症和溶血性贫血。1%的患者在SLE诊断前患有严重溶血性贫血,2.5%的患者出现这些血液学疾病。溶血性贫血和血小板减少症与肾脏受累(0.01 > P > 0.001)和抗心磷脂抗体(ACL)(0.01 > P > 0.001)相关,但与抗双链DNA抗体无关。在严重血液学危机时计算BILAG指数表明,肾脏、中枢神经系统受累和全身症状更常见。41%的患者在事件发生时已在服用泼尼松龙(<10 mg)或免疫抑制剂。

结论

我们的数据表明,溶血性贫血和血小板减少症均与ACL相关,但与抗双链DNA抗体无关。当面对狼疮严重血液学表现的患者时,其他器官可能存在活动性疾病。

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