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小巨核细胞碱性磷酸酶抗碱性磷酸酶染色在血液病中的鉴别诊断意义 被引量:5

Significance of APAAP Staining of Small Megakaryocyte in Differential Hematic Disease
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摘要 目的:研究小巨核细胞(SMK)碱性磷酸酶抗碱性磷酸酶(APAAP)染色在贫血、骨髓增生异常综合征(MDS)中的鉴别诊断意义。方法:应用抗血小板膜糖蛋白ⅡbⅢa(CD41a)单克隆抗体对238例血液病的骨髓片进行APAAP染色并镜检。结果:分别用瑞氏和APAAP两种染色方法计数全片的巨核细胞,两者差异有显著性(P<0.01),后者明显优于前者。各疾病组SMK阳性率由高到低依次为MDS>特发性血小板减少性紫癜(ITP)>原发性血小板增多症(ET)>巨幼细胞贫血(MgA)>肿瘤转移>巨核细胞生成血小板不良>骨髓纤维化症(MF)>混合性贫血>继发性贫血>溶血性贫血(HA)>缺铁性贫血(IDA),再生障碍性贫血未见SMK;MDS组、MgA组和ITP组在SMK类型方面有显著性差异(P<0.05)。结论:APAAP染色有助于识别SMK;SMK的数量及类型变化对贫血的分类、MDS的诊断有一定的鉴别诊断意义,为早期治疗提供了可靠的依据。 Objective:To study the significance of small megakaryocyte(SMK) by APAAP staining in differential diagnosis of anemias and MDS. Methods:The bone marrow smear of 238 patients were stained by APAAP technique and using anti-platelet membrane glycoprotein Ⅱb-Ⅲa (CD41a) monoclonal antibody.The SMK of each marrow smear were counted and classified according to morphologic characteristic. Results:Compared with Wright’s staining, APAAP staining of SMK in all bone marrow smears had a significant difference(P<0.01). The positive rate in turn of SMK of every disease group was MDS>ITP>ET>MgA>Metastatic carcinoma in bone marrow>The platelet production of megakaryocytes is lack>MF>mixed anemia>secondary anemia> HA>IDA. There was a significant difference in the type of SMK among the group of MDS,MgA and ITP(P<0.05). Conclusion:APAAP staining is contributed to identify SMK. Variety of the quantities and types will provide a reliable evidence for differential diagnosis of anemias and MDS.
出处 《江苏大学学报(医学版)》 CAS 2005年第2期142-144,共3页 Journal of Jiangsu University:Medicine Edition
关键词 小巨核细胞 碱性磷酸酶抗碱性磷酸酶染色 血液病 鉴别诊断 Small megakaryocytes APAAP staining Hematic disease Differential diagnosis
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  • 1邵宗鸿,施均,陈桂彬,李克,刘鸿,张益枝,郑以州,和虹,赵明峰,何广胜,张泓,储榆林,郝玉书.白血病前期患者临床及实验室特征的研究[J].中华血液学杂志,2000,21(4):182-186. 被引量:25
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  • 3Harris N,Jaffe E, Diebold J, et al. World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues:Report of the clinical Advisory committee meeting Airlie House, Virginia, November 1997 [ J]. J Clin Oncol, 1999,17:3835 - 3849.

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