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髓过氧化物酶阳性、髓系表面抗原阴性的急性髓系白血病中t(8;21)(q22;q22)的存在情况。

Presence of t(8;21)(q22;q22) in myeloperoxidase-positive, myeloid surface antigen-negative acute myeloid leukemia.

作者信息

Arber D A, Glackin C, Lowe G, Medeiros L J, Slovak M L

机构信息

Division of Pathology, City of Hope National Medical Center, Duarte, California 91010, USA.

出版信息

Am J Clin Pathol. 1997 Jan;107(1):68-73. doi: 10.1093/ajcp/107.1.68.

Abstract

Although acute myeloid leukemias (AMLs) cytochemically negative for myeloperoxidase are now well recognized, myeloid surface antigen-negative AMLs are rare. The morphologic, cytochemical, immunologic, and cytogenetic or molecular features of such cases are described in four adults aged 19 to 60 years. All had AML with maturation (FAB M2) and were myeloperoxidase positive. Immunologic studies showed all to be HLA-DR positive but negative for the CD13, CD14, and CD33 antigens. Two of four were CD34 antigen positive. Cytogenetic studies were performed in three patients, and all demonstrated t(8;21)(q22;q22). In studies using the reverse transcriptase polymerase chain reaction in two patients, including the patient in whom karytypic analysis was not performed, the AML1-ETO fusion product of t(8;21) was identified. These findings suggest an association between the lack of myeloid antigen expression in myeloperoxidase-positive AML and the presence of t(8;21). In addition, the results demonstrate the continued need for cytochemical studies in the evaluation of acute leukemias.

摘要

虽然髓过氧化物酶细胞化学染色阴性的急性髓系白血病(AML)现已得到充分认识,但髓系表面抗原阴性的AML却很罕见。本文描述了4例年龄在19至60岁的成年人此类病例的形态学、细胞化学、免疫学以及细胞遗传学或分子特征。所有患者均为伴有成熟的AML(FAB M2)且髓过氧化物酶呈阳性。免疫学研究显示所有患者HLA - DR均为阳性,但CD13、CD14和CD33抗原呈阴性。4例中有2例CD34抗原呈阳性。对3例患者进行了细胞遗传学研究,所有结果均显示为t(8;21)(q22;q22)。在对2例患者(包括未进行核型分析的患者)使用逆转录酶聚合酶链反应的研究中,鉴定出了t(8;21)的AML1 - ETO融合产物。这些发现提示在髓过氧化物酶阳性的AML中,髓系抗原表达缺失与t(8;21)的存在之间存在关联。此外,结果表明在急性白血病评估中持续需要进行细胞化学研究。

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