Saito M, Kuriyama K, Nagai K, Nonaka H, Hata T, Tusima H, Tabata S, Arimura K, Souda H, Nakamura H
Department of Hematology, Nagasaki University School of Medicine.
Rinsho Ketsueki. 1994 Nov;35(11):1297-304.
We examined leukemic blasts from 5 cases of AML-M0 diagnosed according to The French-American-British (FAB) classification for expression of immunological markers as well as myeloperoxidase (MPO) using flow cytometry (FCM) and immunocytochemistry (ICC). In one patient, the myeloid antigens, CD13 and CD33, were negative on FCM, but apparently positive in the cytoplasm by ICC, leading to a diagnosis of AML-M0. We examined MPO with anti-MPO monoclonal antibody in four patients by ICC, and could detect 3% or more MPO positive rates in all cases. These findings indicate that immunological studies for MPO and myeloid markers using ICC are very useful for the diagnosis of AML-M0. Two of 5 patients achieved CR, but they relapsed soon or after one year, respectively. The treatment outcomes suggest that the AML-M0 is an AML subtype with poor prognosis.
我们根据法国-美国-英国(FAB)分类标准,对5例诊断为AML-M0的急性髓系白血病原始细胞进行了检测,采用流式细胞术(FCM)和免疫细胞化学(ICC)检测免疫标志物以及髓过氧化物酶(MPO)的表达情况。在1例患者中,髓系抗原CD13和CD33在FCM上呈阴性,但通过ICC在细胞质中明显呈阳性,从而诊断为AML-M0。我们通过ICC用抗MPO单克隆抗体检测了4例患者的MPO,所有病例均能检测到3%或更高的MPO阳性率。这些结果表明,使用ICC对MPO和髓系标志物进行免疫学研究对AML-M0的诊断非常有用。5例患者中有2例达到完全缓解(CR),但分别很快或1年后复发。治疗结果表明,AML-M0是一种预后较差的急性髓系白血病亚型。