Parreira L, Tavares de Castro J, Hibbin J A, Marsh J C, Marcus R E, Babapulle V B, Spry C J, Goldman J M, Catovsky D
Br J Haematol. 1986 Apr;62(4):659-69. doi: 10.1111/j.1365-2141.1986.tb04089.x.
A cytogenetic analysis was carried out on bone marrow cells from 11 patients who presented with hypereosinophilia and the clinical features of the idiopathic hypereosinophilic syndrome. One of these patients was found to have trisomy 8 affecting the myeloid series, including eosinophils. In this patient, marrow eosinophils also showed asynchrony of nuclear-cytoplasmic maturation, and there were increased numbers of myeloid progenitor cells in the blood. Six months later, blast cell transformation occurred, and he died soon afterwards. These findings show that abnormalities in the karyotype of bone marrow cells and culture of blood progenitor cells may help to identity eosinophilic leukaemia among patients who present with features of the idiopathic hypereosinophilic syndrome.
对11例表现为嗜酸性粒细胞增多及特发性嗜酸性粒细胞增多综合征临床特征的患者的骨髓细胞进行了细胞遗传学分析。其中1例患者被发现存在8号染色体三体,累及包括嗜酸性粒细胞在内的髓系。在该患者中,骨髓嗜酸性粒细胞还表现出核质成熟不同步,血液中髓系祖细胞数量增加。6个月后发生了原始细胞转化,患者随后不久死亡。这些发现表明,骨髓细胞染色体核型异常及血液祖细胞培养可能有助于在表现为特发性嗜酸性粒细胞增多综合征特征的患者中识别嗜酸性粒细胞白血病。