期刊文献+

表现为大细胞性贫血的再生障碍性贫血病人临床分析

APLASTIC ANEMIA MANIFESTS AS MACROCYTIC ANEMIA:CLINICAL ANALYSIS
下载PDF
导出
摘要 目的探讨表现为大细胞性贫血的再生障碍性贫血(MAA)病人的临床特点。方法回顾性分析55例MAA病人的临床资料,并以同期表现为正细胞性贫血的再生障碍性贫血(NAA)病人127例作为对照。结果MAA组病人的年龄明显高于对照组,差异有显著性(t=3.60,P<0.05);MAA组中非重型再生障碍性贫血(NSAA)病人比例明显偏高,差异有显著性(χ2=52.47,P<0.05);MAA组重型再生障碍性贫血(SAA)病人网织红细胞计数(Ret)显著高于NAA组,差异有显著性(t=2.68,P<0.05);MAA组SAA病人骨髓红系比例高于NAA组,差异有显著性(t′=2.33,P<0.05)。治疗6个月后,MAA组SAA、NSAA病人有效率与NAA组比较差异无显著性(P>0.05)。随访29(1~72)个月,MAA组SAA、NSAA病人生存率与NAA组比较,差异无显著性(P>0.05)。结论与NAA病人比较,MAA病人发病年龄较大,NSAA比例、Ret、骨髓红系比例偏高。 Objective To discuss the clinical features of aplastic anemia (AA) that manifests as macrocytic anemia (MA). Methods Clinical data of 55 patients with MA were reviewed retrospectively, and 127 patients with normocytic anemia (NA) of corresponding time period served as controls. Results The age of patients with MA was markedly older than that of the controls (t=3.60,P〈0.05),in MA, the proportion of non-severe AA patients was higher (gz =52.47,P(0.05) ; the reticulocyte count (Ret) was significantly higher in severe AA than in non-severe AA (t =2.68,P^0.05). In MA, the proportion of erythroid cells in bone marrow was also higher (t'= 2.33, P d0.05). After 6 months of treatment, the difference in effective rate of severe AA and non-severe AA between MA group and NA group was not significant (P〉0.05). A follow-up of 29 (1--72) months showed the difference in survival rate between MA and NA groups was not significant (P〉0.05). Conclusion Compared with normocytic anemia patients, the age of onset in patients with macrocytic anemia is comparatively older, and the proportion of non- severe aplastic anemia, Ret and proportion of erythroid ceils are high.
出处 《齐鲁医学杂志》 2016年第2期216-218,共3页 Medical Journal of Qilu
关键词 贫血 再生障碍性 贫血 大细胞性 治疗结果 anemia, aplastic anemia, macrocytic treatment outcome
  • 相关文献

参考文献9

  • 1李英梅,李星鑫,孙慧,孙玲,万鼎铭,刘林湘,陈胜梅,陈绍倩,刘少君,郑以州,邹典斌.表现为大细胞性贫血的再生障碍性贫血患者长期随访研究[J].中华血液学杂志,2013,34(2):117-121. 被引量:3
  • 2YOSHIZATO T, DUMITRIU B, HOSOKAWA K, et al. So- maticmutations and clonal hematopoiesis in aplastic anemia[J]. N Engl J Med, 2015,373(1):35-47.
  • 3BEUTLERE, LICHTMANMA, COLLERBS, et al. Williams hematology[M]. 6th ed. New York: The McGrew-Hill Com- panies, 2000:328.
  • 4崔中光,汪洪毅,赵洪国.环孢素、司坦唑醇及大剂量甲基泼尼松龙治疗急性再生障碍性贫血的效果[J].青岛大学医学院学报,2003,39(1):97-97. 被引量:3
  • 5再生障碍性贫血诊断治疗专家共识[J].中华血液学杂志,2010,31(11):790-792. 被引量:154
  • 6MARSH J, SCHREZENMEIER H, MARIN P, et al. Pro- spective randomized multicenter study comparing cyclosporin alone versus the combination of antithymocyte globulin and cy- closporin for treatment of patients with non-severe aplastic anemia: a report from the European Blood and Marrow Trans plant (EBMT) [J]. Blood, 1999,93 (7), 2191-2195.
  • 7MARSH J C, HOWS J M, BRYETT K A, et al. Survival af ter antilymphocyte globulin therapy for aplastic anemia de- pends on disease severity[J]. Blood, 1987,70(4) :1046-1052.
  • 8AHN M J, CHOI J H, LEE Y Y, et al. Outcome of adult se- vere or very severe aplastic anemia treated with immunosup- pressive therapy compared with bone marrowtransplantation: multicentertrial[J]. Int J Hematol, 2003,78(2) : 133-138.
  • 9SCHEINBERG P, WU CO, NUNEZ O, et al. Predicting re- sponse to immunosuppressive therapy and survival in severe aplastic anaemia[J]. Br J Haematol, 2009,144(2):206-216.

二级参考文献12

  • 1陈寿权,张君丽.环孢霉素A和大剂量甲基泼尼龙治疗重型再生障碍性贫血[J].中华血液学杂志,1996,17(8):422-423. 被引量:14
  • 2田永军,胡慧萍,刘建梅,孙汉英.156例再生障碍性贫血临床分析[J].实用诊断与治疗杂志,2007,21(6):466-468. 被引量:14
  • 3Vardiman JW, Thiele J, Arber DA, et al. The 2008 revision of the World Health Organization ( WHO ) classification of myeloid neoplasms and acute leukemia: rationale and important changes. Blood, 2009,114: 937-951.
  • 4Kojima S, Matsuyama T, Kodera Y. Circulating erythropoietin in patients with acquired aplastic anaemia. Acta Haematol, 1995, 94 : 117-122.
  • 5Beutler E, Lichtman MA, Coller BS, et al. Williams Hematology.6th ed. New York:The McGrew-Hill Companies, 2000:328.
  • 6Kojima S, Hibi S, Kosaka Y, et al. Immunosuppressive therapy using antithymoeyte globulin, cyclosporine, and danazol with or without human granuloeyte colony-stimulating factor in children with acquired aplastic anemia. Blood, 2000, 96:2049-2054.
  • 7Ohga S, Ohara A, Hibi S, et al. Treatment responses of childhood aplastie anaemia with chromosomal aberrations at diagnosis. Br J Haematol. 2002. 118:313-319.
  • 8Afable II MG, Tiu RV, Maciejewski JP. Clonal Evolution in Aplastic Anemia. Hematology Am Soc Hematol Educ Program, 2011:90-95.
  • 9Bagby GC, Meyers G. Bone marrow failure as a risk factor for clonal evolution: prospects for leukemia prevention. Hematology Am Soc Hematol Educ Program, 2007: 40-46.
  • 10李英梅,刘旭平,李承文,徐方运,贡金英,于成龙,王建祥,郑以州.应用间期荧光原位杂交研究再生障碍性贫血单体7克隆性演变[J].中华血液学杂志,2010,31(10):688-692. 被引量:4

共引文献157

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