期刊文献+

系统性红斑狼疮患者血液学异常的特点及其临床意义 被引量:19

Hematological abnormalities in systemic lupus erythematosus and clinical significance thereof:comparative analysis of 236 cases
原文传递
导出
摘要 目的探讨系统性红斑狼疮(SLE)患者血液系统异常的特点及其临床意义。方法236例新诊断的SLE住院患者,其中血红蛋白≤100g/L者设为贫血组;根据白细胞计数分为2组,白细胞计数〈3.0×10^9/L者为WBC1组,白细胞计数3.0~3.9×10^9/L为WBC2组;血小板〈100×10^9/L设定为血小板减少组。无血液学异常者设定为对照组。结果贫血的患者123例,占52.1%。造成贫血的原因主要有:慢性病贫血(ACD),82例,溶血性贫血(HA),18例,造血功能异常8例,原因未明,15例。外周血有白细胞下降者73例,占30.9%。血小板下降57例,占24.2%。无血液学异常68例,占28.8%。其中溶血性贫血组、WBC1组和血小板减低组狼疮活动指标明显高于对照组。对72例患者做了骨髓细胞形态学检查,49例是正常骨髓象,10例患者骨髓有不同程度的病态造血,2例表现骨髓巨核细胞缺乏,9例表现为骨髓三系造血增生低下,有2例表现出单纯红系造血低下。结论中国SLE患者贫血比例较高的主要原因可能是慢性病贫血患者的比例明显高于国外。SLE患者溶血性贫血比例较低,但却是SLE疾病活动很重要的指征。白细胞计数〈3.0×10^9/L和血小板下降也与SLE活动有关。部分患者骨髓造血异常是引起较严重血液学改变的原因之一。 Objective To investigate the hematological abnormalities and their relationship to the disease activity of systemic lupus erythematosus ( SLE ). Methods The clinical data of 236 SLE patients, 29 males and 207 females with the age of confirmed diagnosis of 33.4, were divided into 3 groups : anemia group, with the hemoglobin (Hgb) 〈 100 g/L, including 2 subgroups, i.e. subgroup of anemia caused by chronic diseases (ACD) and subgroup of hemolytic anemia; low white blood cell group 1 (Group WBC1 ) with the WBC count 〈4.0 × 10^9/L, white blood cell group 2 ( Group WBC2) with the WBC count 3.0~3.9 × 10^9/L, immune thrombopenic purpura group ( ITP group) with a platelet count 〈 100 × 10^9/L, and control group without hematological changes. 72 patients underwent morphologic characterization of their bone marrow. The hematological data and the relationship thereof to the disease activity in different groups were analyzed. Results Among the 236 SLE patients 168 (71.18%) had hematological abnormalities and 68 of them (28. 82% ) without hematological abnormalities. 123 of the 168 patients with hematological abnormalities (52. 1% ) had anemia, 82 of which (66. 7 % ) had characteristics of anemia caused by chronic diseases, 18 (14.6%) had hemolytic anemia, 8 (6.6%) had hematopoietic abnormalities, and the remaining 15 patients (12%) had anemia caused by unknown reasons. 73 of the 236 SLE patients (30. 9% ) had a WBC count 〈4. 0 × 10^9/L and 57 patients (24. 2% ) had a platelet count 〈 100 × 10^9/L. In the groups with hemolytic anemia, WBC count 〈 3.0 × 10^9/L and thrombocytopenia, the complement levels were significant lower, and the levels of C-reactive protein (CRP) and positive anti-dsDNA antibody were significantly higher than those of the controls ( all P 〈 0.05 ) The rate of positive antiphospholipid antibody of the hemolytic anemic patients and patients with thrombocytopenia were 22. 2% and 15.8% respectively, both significantly higher than that of the controls (2. 9%, both P 〈 0. 05 ). 49 of the 72 patients undergoing morphologic characterization of bone marrow had normal cell morphology and a normal appearing bone marrow, 10 had varying degrees of pathologic hematopoietic changes, 2 lacked megakaryocytes, 9 expressed decreased proliferation in all three hematopoietic lineages, and 2 had only a decrease in erythropoiesis. Conclusion The reason of the high proportion of anemia among the SLE patients in China may be the higher proportion of anemia caused by ACD in comparison with that abroad. Although SLE patients have lower rates of hemolytic anemia, HA is an important index of SLE disease activity. Thrombocytopenia and a WBC count 〈 3.0 × 10^9/L are related to SLE disease activity. Abnormalities of hemopoiesis by bone marrow is one of the reasons of sever hematological changes in part of the SLE patients.
出处 《中华医学杂志》 CAS CSCD 北大核心 2007年第19期1330-1333,共4页 National Medical Journal of China
关键词 系统性红斑狼疮 血液学 骨髓 临床意义 Systemic lupus erythematosus Hematology Bne marrow
  • 相关文献

参考文献14

  • 1李蓉生.慢性病贫血//张之南,沈悌,主编.血液病诊断及疗效标准.2版.北京:科学出版社,1998:30-33.
  • 2陈嘉林,李淑兰,徐闽,王海滨,葛昌文,李蓉生.血清转铁蛋白受体对贫血患者鉴别诊断的临床意义[J].中华内科杂志,2004,43(6):423-425. 被引量:12
  • 3Font J, Cervera R, Ramos-Casals M, et al. Clusters of Clinical and Features in Systemic lupus erythematosus: Analysis of 600 patients from a single center. Semin Arthritis Rheum, 2004,33: 217 -230.
  • 4张幼莉,张学武,贺联印.系统性红斑狼疮相关性血液学异常[J].临床内科杂志,1998,15(3):160-161. 被引量:28
  • 5Hoohberg MC, Boyd RE , Ahearn JM, et al. Systemic lupus erythematosus : a review of Clinico-laboratory feature and immunogenetic markers in 150 patients with emphasis on demographic subets . Medicine, 1985,64:285-295.
  • 6Voulgarelis M, Kokori SIG, Ioannidis JAP, et al. Anaemia in systemic lupus erythematosus: aetiological profile and the role of erythropoietin. Ann Rheum Dis, 2000, 59: 217-222.
  • 7Keeling DM, Isonberg DA. Hematological manifestations of systemic lupus erythematosus. Blood Reviews, 1993, 7: 199- 207.
  • 8Pistiner M ,Wallace DJ ,Nessim S,et al. Lupus erythematosus in the 1980s: a Survey of 570 patients . Semin Arthritis Rheum, 1991, 21:55-64.
  • 9Kasitanon N, Magder LS, Petri M. Predictors of survival in systemic lupus erythematosus. Medicine, 2006, 85:147-156.
  • 10Matsugama W, Yamamoto M, Higashimoto I, et al. TNF-related apoptosis-inducing ligand is involved in neutropenia of systemic lupus erythematosus. Blood, 2004,104 : 184-191.

二级参考文献5

  • 1Das Gupta AM, Abbi A. High serum transferrin receptor level in anemia of chronic disorders indicates coexistent iron deficiency. Am J Hematol, 2003,72, 158-161.
  • 2Worwood M. Serum transferring receptor assays and their application. Ann Clin Biochem, 2002, 39(Part 3): 221-230.
  • 3Fitzsimons EJ, Houston T, Munro R, et al. Erythroblast iron metabolism and serum soluble transferrin receptor values in the anemia of rheumatoid arthritis. Arthritis Rheum, 2002, 47,166-171.
  • 4林果为.铁代谢的研究进展和相关疾病关系,第十届全国贫血学术会议汇编[Z].桂林,2003,1..
  • 5白砚霞,李蓉生,陈嘉林,李琦.应用综合性铁指标对慢性病贫血及缺铁性贫血的诊断评估[J].中华血液学杂志,1999,20(6):329-330. 被引量:8

共引文献39

同被引文献157

引证文献19

二级引证文献77

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部