Raimondi R, Pellizzari G, Rodeghiero F
Department of Hematology, San Bortolo Hospital, Vicenza, Italy.
Haematologica. 1993 Nov-Dec;78(6 Suppl 2):66-72.
Immunophenotyping is at present a useful aid and often an essential step for correct diagnosis of acute leukemia and for this purpose some investigators have proposed several immunomarker panels. This approach is particularly important in the differential diagnosis of acute leukemias not classifiable by standard morphology and cytochemistry.
We have tested peripheral blood and/or bone marrow samples from 125 patients not classifiable by FAB criteria. In all the cases, the reactivities of the same panel of 17 monoclonal antibodies were analyzed by flow cytometry, using both single and double fluorescent labeling.
Of the 125 patients investigated, 75 (60%) were classifiable as ALL, 58 as B-lineage ALL and 17 as T-lineage ALL; 33 (26.4%) as AML, of which 2 M7; 6 (4.8%) as biphenotypic and 11 (8.8%) as immunophenotypically undifferentiated.
From a critical analysis of our cases and a review of the literature, we suggest that a panel of 9 monoclonal antibodies (CD2, CD5, CD7, CD10, CD19, CD20, CD13, CD33, CD41), is sufficient for reliable, rapid and reasonably low cost typing of acute leukemia, useful for an immediate therapeutic decision.
免疫表型分析目前是正确诊断急性白血病的一项有用辅助手段,且常常是关键步骤,为此一些研究者提出了多种免疫标志物组合。这种方法在无法通过标准形态学和细胞化学进行分类的急性白血病的鉴别诊断中尤为重要。
我们检测了125例不符合FAB标准的患者的外周血和/或骨髓样本。所有病例均采用单荧光和双荧光标记,通过流式细胞术分析同一组17种单克隆抗体的反应性。
在125例受调查患者中,75例(60%)可分类为急性淋巴细胞白血病(ALL),其中58例为B系ALL,17例为T系ALL;33例(26.4%)为急性髓系白血病(AML),其中2例为M7;6例(4.8%)为双表型,11例(8.8%)免疫表型未分化。
通过对我们的病例进行批判性分析并回顾文献,我们建议一组9种单克隆抗体(CD2、CD5、CD7、CD10、CD19、CD20、CD13、CD33、CD41)足以对急性白血病进行可靠、快速且成本合理的分型,有助于立即做出治疗决策。