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CD117在急性白血病鉴别诊断中的诊断价值。

Diagnostic value of CD117 in differential diagnosis of acute leukemias.

作者信息

Ahmadi Abbas, Poorfathollah Ali-Akbar, Aghaiipour Mahnaz, Rezaei Mansour, Nikoo-ghoftar Mahin, Abdi Mohammad, Gharib Alireza, Amini Amir

机构信息

Cellular and Molecular Research Center, Kurdistan University of Medical Sciences, Pasdaran Boulevard, Sanandaj, Iran,

出版信息

Tumour Biol. 2014 Jul;35(7):6763-8. doi: 10.1007/s13277-014-1899-8. Epub 2014 Apr 11.

Abstract

C-kit receptor (CD117) and its ligand, stem cell factor, play a key role in normal hematopoiesis. It has been demonstrated that its expression extremely increases in leukemias with myeloid commitment. We analyzed findings on CD117 expression together with other myeloid related markers in 203 de novo acute leukemias, referred to Iranian immunophenotyping centers: Iranian Blood Transfusion Organization (IBTO) and Baghiatallah Hospital (BH). All cases were characterized based on the French American British cooperative group (FAB) and European Group for Immunological Classification of Leukemias (EGIL). The cases comprised of 111 acute myeloblastic leukemia (AML), 86 acute lymphoblastic leukemia (ALL), and 6 acute undifferentiated leukemia (AUL). CD117 was positive in 75 % of AML and 50 % of AUL, whereas none of the ALL cases was positive for this marker. Although CD117 was positive in 100 % of M5a cases, no M5b positive was found (p = 0.036). The calculated specificity for myeloid involvement was 100 % for CD117 and CD33, and 98 % for CD13 and CD15 (p < 0.001). The calculated sensitivity for myeloid involvement was 83, 76, 64, and 41 % for CD13, CD117, CD33, and CD15, respectively (p < 0.001). We concluded that CD117 expression is a specific and rather sensitive marker for differential diagnosis between AML and ALL, and except for M5 subtypes, it fails to determine FAB subtypes; lack of expression in M5 can identify M5b. Therefore, it should be included in the routine primary panel for diagnosis of acute leukemias.

摘要

C-kit受体(CD117)及其配体干细胞因子在正常造血过程中发挥关键作用。已有研究表明,在具有髓系定向的白血病中其表达极度增加。我们分析了伊朗免疫表型分析中心(伊朗输血组织(IBTO)和巴吉亚塔拉医院(BH))送检的203例初发急性白血病中CD117表达及其他髓系相关标志物的检测结果。所有病例均根据法国-美国-英国协作组(FAB)和欧洲白血病免疫分类组(EGIL)进行分类。病例包括111例急性髓细胞白血病(AML)、86例急性淋巴细胞白血病(ALL)和6例急性未分化白血病(AUL)。CD117在75%的AML和50%的AUL中呈阳性,而所有ALL病例中该标志物均为阴性。尽管CD117在100%的M5a病例中呈阳性,但未发现M5b阳性病例(p = 0.036)。计算得出CD117和CD33对髓系受累的特异性为100%,CD13和CD15为98%(p < 0.001)。计算得出CD13、CD117、CD33和CD15对髓系受累的敏感性分别为83%、76%、64%和41%(p < 0.001)。我们得出结论,CD117表达是AML和ALL鉴别诊断的特异性且相当敏感的标志物,除M5亚型外,它无法区分FAB亚型;M5中缺乏表达可识别M5b。因此,它应纳入急性白血病诊断的常规初筛检测项目中。

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