Broustet A, Bernard P, Dachary D, David B, Marit G, Lacombe F, Issanchou A M, Reiffers J
Cancer Genet Cytogenet. 1986 Apr 15;21(4):327-33. doi: 10.1016/0165-4608(86)90213-x.
Eosinophilic leukemias are difficult to individualize amid the hypereosinophilic syndromes. Chromosomal abnormalities when present within the eosinophils are of critical value in the diagnosis of a malignancy. We report here the case of a 27-year-old woman who had been healthy, until recently when she suddenly developed hepatosplenomegaly and lymph node enlargement, and considerable eosinophilia in blood and bone marrow. The morphologically abnormal cells (large pseudo Pelger eosinocytes) predominated in the cytology. The establishment in these cells of a clonal chromosomal anomaly, t(10;11)(p14;q21), favored the malignancy and diagnosis of acute eosinophilic leukemia.
在高嗜酸性粒细胞综合征中,嗜酸性粒细胞白血病难以个体化诊断。嗜酸性粒细胞内出现的染色体异常对恶性肿瘤的诊断具有关键价值。我们在此报告一例27岁女性病例,该患者此前一直健康,直到最近突然出现肝脾肿大、淋巴结肿大,血液和骨髓中出现大量嗜酸性粒细胞增多。细胞学检查显示形态异常的细胞(大的假佩尔格嗜酸性粒细胞)占主导。这些细胞中克隆性染色体异常t(10;11)(p14;q21)的发现支持了急性嗜酸性粒细胞白血病的恶性肿瘤诊断。