期刊文献+

难治性贫血与白血病前期——92例分析 被引量:16

Refractory anemia and preleukemia:an analysis of 92 cases
原文传递
导出
摘要 目的探讨骨髓增生异常综合征(MDS)中的难治性贫血(RA)亚型和白血病前期(白前)的关系。方法对86例RA和6例不符合RA诊断标准的白前病例进行回顾性分析。结果将34例(39.53%)转化为急性白血病(AL)、原始细胞增多的RA(RAEB)和转变中的RAEB(RAEBt)者定为转化组,其余52例为未转化组。与未转化组比较,转化组有下列血液学特征:①外周血中、晚幼粒细胞,有核红细胞和巨大红细胞出现频率较高,中性粒细胞明显核左移;②骨髓原始和早幼阶段的粒系和红系细胞比例较高,三系常同时有血细胞发育异常的形态改变,3核以上红细胞、假性PelgerHuet异常及淋巴样小巨核细胞出现率亦较高。结论按现行RA标准诊断的病例与白前有较大重叠,上述转化组的血液学特征对RA向AL转化可能有一定预示作用。根据结果,提出一个预测RA转化的积分系统。 Objective To investigate the relationship between MDS RA (refractory anemia subtype of myelodysplastic syndromes) and preleukemia (PL). Methods Hematological parameters of 86 RA and 6 PL patients were retrospectively analyzed. Results Thirty four RA cases (39.53%) transformed into acute leukemia (AL), RA with excess blasts (RAEB), or RAEB in transformation (RAEB t). As compared with 52 non transformed RA cases , the transformed cases showed the following hematological features: ①higher frequencies of immature granulocytes (P<0.005),erythroblasts (P<0.05) and megaloerythrocytes (P<0 05), and higher granulocyte nuclear lobulation (P<0.001) in peripheral blood; ②higher percentages of early erythroid and granulocytic lineages (P<0.05), and higher frequencies of erythroblasts with multiple nuclei (P<0.05),pseudo Pelger Huet abnormality (P<0.05),and micromegakaryocytes (P<0.005) in bone marrow. Conclusion There is a higher overlap between RA and PL; the above hematological features may be useful for predicting the transformation of RA patients. Based on those findings, a score system for predicting the transformation of RA was proposed.
出处 《中华血液学杂志》 CAS CSCD 北大核心 1999年第2期65-68,共4页 Chinese Journal of Hematology
关键词 贫血 骨髓增生异常 综合征 白血病前期 病例分析 Anemia, refractory Myelodysplastic syndromes Preleukemia
  • 相关文献

参考文献2

  • 1郝玉书 张源慧 等.天津地区1677名健康人血象的调查报告Ⅲ:中性粒细胞分类及气候条件对它的影响[J].天津医药,1960,2:582-587.
  • 2郝玉书,天津医药杂志,1960年,2卷,582页

同被引文献36

  • 1史青,粟军,余江,蒋能刚.骨髓增生异常综合征的WHO分型特点[J].国外医学(临床生物化学与检验学分册),2005,26(10):767-768. 被引量:6
  • 2李昕权.铁代谢中铁蛋白、转铁蛋白及相关基因调节的研究进展[J].中华血液学杂志,1996,17(6):329-331. 被引量:5
  • 3马金龙,吴岚岚,杜海珍,陈宝安,丁家华,高冲,孙耘玉.46例骨髓增生异常综合征形态学分析[J].国际检验医学杂志,2007,28(2):181-181. 被引量:4
  • 4[3]Bennett JM.World Health Organizmtion classification of the acute leukemias and the myelodysplastic syndromes[J].Int JHemotal,2000,72(2):131
  • 5张之楠,沈悌.血液病诊断及疗效标准[M].3版.北京:科学出版社,2007:271-271.
  • 6Bennet JM, CatovskyD, Daniel MT, et al. The French - American -British Cooperative Group. Proposals for the classification of the myelodysplastic syndrome[ J}. Brit J Haematol,1982 ,51:189 - 199.
  • 7Kuiper EP, Coenen JL, Huisman CM, et al. Relationship between soluble transferrin receptors in serum and membrane - bound transferrin receptors[J]. Acta Haematol,1998,99(1) :8 - 11.
  • 8Cortelezzi A, Cattaneo C, Cristiani S, et al. Non- transferrin bound iron in myelodysplastic syndromes:a marker of ineffecfive erythropoiesis [J]. Hematol J,2000,1(3) :153 - 158.
  • 9许国王宣.内科讲座 骨髓检查[M]第6版[M].北京:人民卫生出版社,1984-7..
  • 10Sole F, Espinet B, Sanz GF et al. Incidence, characterization and prognostic significance of chromosomal abnormalities in 640 patients with primary myelodysplastic syndromes. British Journal of Haematology, 2000;108:347~55

引证文献16

二级引证文献37

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