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摘要: 目的:分析CD1a-/CD8-、My/S+及CD5weak对早期前体T淋巴母细胞白血病(ETP-ALL)诊断的意义及与临床特点的关系,以提高对ETP-ALL免疫表型及临床特点的认识。方法:回顾性分析55例初诊急性T淋巴细胞性白血病患者的流式免疫分型结果,分析CD1a-/CD8-、My/S+、CD5weak及ETP与各抗原表达阳性率的关系,以及CD1a-/CD8-、My/S+和CD5weak两两联合对ETP诊断特异性的影响,并比较ETP(CD1a-/CD8-、My/S+、CD5weak),near ETP(CD1a-/CD8-、My/S+、CD5+++)及其他(others)组的临床基本特点。结果:多数抗原表达阳性率在CD1a-/CD8-和not CD1a-/CD8-组间、My/S+和My/S-组间及ETP和non ETP组间均差异有统计学意义。但在CD5weak和CD5+++组间,各抗原表达阳性率均差异无统计学意义。CD1a-/CD8-联合My/S+对ETP的诊断特异度为75.8%,CD5weak联合CD1a-/CD8-或My/S+对ETP的诊断特异度均为90.9%。ETP,near ETP及others组年龄、白细胞计数及血小板计数均差异有统计学意义。结论:CD1a-/CD8-、My/S+对ETP-ALL的识别与诊断具有重要意义,CD5weak在ETP-ALL的鉴别诊断中具有重要价值,需要注意将符合CD1a-/CD8-、My/S+,但CD5高表达的near ETP患者区分出来。ETP及near ETP均具有较独特的临床特点。
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关键词:
- 淋巴母细胞白血病/淋巴瘤 /
- 早期前体T淋巴母细胞白血病 /
- 免疫表型
Abstract: Objective:To analyze the significance of CD1a-/CD8-,My/S+ and CD5weak in the diagnosis of early T-cell precursor acute lymphoblastic leukemia (ETP-ALL) and their relationship with clinical characteristics,so as to improve the understanding of the immunophenotype and clinical characteristics of ETP-ALL.Method:The results of immunophenotype in 55 patients with newly diagnosed acute T-lymphoblastic leukemia were retrospectively was analyzed.The relationship between CD1a-/CD8-,My/S+,CD5weak,ETP and the positive ratio of different antigens was analyzed.The effects of CD1a-/CD8-,My/S+,and CD5weak on the specificity of ETP diagnosis were compared.Furthermore,basic clinical characteristics of ETP (CD1a-/CD8-,My/S+,CD5weak),near ETP (CD1a-/CD8-,My/S+,CD5+++) and other groups were compared.Result:The positive rates of most antigens were significantly different between CD1a-/CD8- vs not CD1a-/CD8- group;My/S+ vs My/S- group and ETP vs non-ETP group.However,there was no significant difference of the positive rate of each antigen between CD5weak and CD5+++ group.The diagnostic specificity of CD1a-/CD8- combined with My/S+ for ETP was 75.8%,and that of CD5weak combined with CD1a-/CD8- or My/S+ for ETP was 90.9%.There were significant differences in age,leukocyte count and platelet count among ETP,near ETP and other group.Conclusion:CD1a-/CD8- and My/S+ have great significance in the identification and diagnosis of ETP-ALL.CD5weak has great value in the differential diagnosis of ETP-ALL.It is necessary to distinguish near ETP patients with CD1a-/CD8-,My/S+ and elevated CD5.Both ETP and near ETP have unique clinical characteristics. -
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