Hogge D E, Misawa S, Parsa N Z, Pollak A, Testa J R
J Clin Oncol. 1984 Jun;2(6):550-7. doi: 10.1200/JCO.1984.2.6.550.
Six patients with M4 acute myelomonocytic leukemia ( AMMoL ) were identified who had abnormalities of chromosome 16 in bone marrow cells. Five had a pericentric inversion, inv(16)( p13q22 ), and a sixth patient had a translocation, t(16;16)(p13.1;q22). Each of these six patients had bone marrow eosinophils that were abnormal in morphology on light and/or electron microscopy and by cytochemical stains. The eosinophils constituted 1%-24% of nucleated marrow cells. Of 61 acute nonlymphocytic leukemia (ANLL) patients, all those with AMMoL and abnormal bone marrow eosinophils had an inv(16) or a t(16;16). One other patient in this group had a rearrangement of chromosome 16 (with a break in the short arm at band p13); however, the ANLL type was M1 and no abnormal eosinophils were present. Four patients with ANLL types other than M4 had an increase in marrow eosinophils; three in whom the eosinophils appeared normal and one with ANLL-M2 and bizarre eosinophils morphologically distinct from those seen in AMMoL . Chromosome pair 16 was normal in the latter four patients. AMMoL with dysplastic bone marrow eosinophils appears to represent a unique clinicopathologic entity associated with several related abnormalities affecting 16q . The morphologic features of both blasts and eosinophils may be more important than the absolute number of eosinophils in the marrow in identifying this group of patients. This may have prognostic importance as five of six patients achieved complete remission with standard antileukemic therapy and are still alive.
6例M4型急性粒单核细胞白血病(AMMoL)患者被确诊,其骨髓细胞存在16号染色体异常。5例患者有臂间倒位,inv(16)(p13q22),第6例患者有易位,t(16;16)(p13.1;q22)。这6例患者的骨髓嗜酸性粒细胞在光镜和/或电镜下以及通过细胞化学染色显示形态异常。嗜酸性粒细胞占骨髓有核细胞的1% - 24%。在61例急性非淋巴细胞白血病(ANLL)患者中,所有患有AMMoL且骨髓嗜酸性粒细胞异常的患者均有inv(16)或t(16;16)。该组中的另1例患者有16号染色体重排(短臂在p13带处断裂);然而,ANLL类型为M1,且不存在异常嗜酸性粒细胞。4例非M4型ANLL患者骨髓嗜酸性粒细胞增多;其中3例嗜酸性粒细胞外观正常,1例为ANLL - M2,其奇异嗜酸性粒细胞在形态上与AMMoL中所见不同。后4例患者的16号染色体对正常。伴有发育异常骨髓嗜酸性粒细胞的AMMoL似乎代表一种独特的临床病理实体,与影响16q的几种相关异常有关。在识别这组患者时,原始细胞和嗜酸性粒细胞的形态特征可能比骨髓中嗜酸性粒细胞的绝对数量更重要。这可能具有预后意义,因为6例患者中有5例通过标准抗白血病治疗实现了完全缓解且仍然存活。