Bernard P, Dachary D, Reiffers J, Marit G, Wen Z, Jonveaux P, David B, Lacombe F, Broustet A
Laboratorie d'Hématologie, Centre Hospitalier Régional, Bordeaux, France.
Leukemia. 1989 Oct;3(10):740-5.
This article reports 18 cases of acute nonlymphocytic leukemia (ANLL) and abnormal chromosome 16. Thirteen had the same hematological pattern at diagnosis, i.e., peripheral blood hyperleukocytosis with high percentage of monocytes and blast cells, and bone marrow showing three different cell populations: (a) myeloblasts, (b) monocytes and promonocytes, and (c) abnormal eosinophils. In these cases the diagnosis was acute myelomonocytic leukemia with bone marrow eosinophilia, as described. However three other cases were of the M5 type and two others of the M2 type, all showing an abnormal eosinophilia in their bone marrow. All cases showed an abnormal chromosome 16 in the bone marrow cells: inv (16) in 13 cases, t (16;16) in two, del (16) in one of poor quality, and in two other translocations involving band 16q22. In one case the inv (16) was found in a subclone, indicating that it could be a secondary cytogenetic defect. Five patients died soon after diagnosis; the other 13 had a median complete remission duration of 8 months. The central nervous system was frequently involved upon relapse. We do not support the hypothesis that patients with M4-Eo ANLL and chromosome 16 abnormality have a favorable prognosis.
本文报告了18例急性非淋巴细胞白血病(ANLL)及16号染色体异常的病例。其中13例在诊断时具有相同的血液学模式,即外周血白细胞增多,单核细胞和原始细胞比例较高,骨髓显示三种不同的细胞群:(a)原始粒细胞,(b)单核细胞和幼稚单核细胞,以及(c)异常嗜酸性粒细胞。在这些病例中,诊断为如所述的伴有骨髓嗜酸性粒细胞增多的急性粒单核细胞白血病。然而,另外3例为M5型,2例为M2型,所有病例骨髓均显示异常嗜酸性粒细胞增多。所有病例骨髓细胞均显示16号染色体异常:13例为inv(16),2例为t(16;16),1例质量较差为del(16),另外2例为涉及16q22带的其他易位。1例病例中inv(16)存在于一个亚克隆中,表明其可能是继发性细胞遗传学缺陷。5例患者在诊断后不久死亡;其他13例患者的完全缓解期中位数为8个月。复发时中枢神经系统常受累。我们不支持M4-Eo ANLL伴16号染色体异常的患者预后良好这一假说。