Harousseau J L, Smadja N, Krulik M, Audebert A A, Debray J
Nouv Presse Med. 1978 Nov 4;7(38):3431-5.
Twenty-four patients, in a condition considered to be pre-leukaemic underwent study of marrow caryotype. Nine of them (37.5%) had an abnormal caryotype. The prevalence of abnormalities varied according to the type of pre-leukaemic state: 17% in acquired idiopathic sideroblastic anaemia, 33% in refractory anaemias with excessive myeloblasts, 100% in 3 cases of simple refractory anaemia. The abnormalities were non-systematised. However, in one case there was an abnormality already described in the literature and considered to be specific: deletion of the long branch of chromosome 5. In refractory anaemias with excess myeloblasts transformation to acute leukaemia appeared to be more frequent in patients with an abnormality (4/5) than in patients with a normal caryotype (0/10).
24例被认为处于白血病前期的患者接受了骨髓核型研究。其中9例(37.5%)核型异常。异常的发生率根据白血病前期状态的类型而有所不同:获得性特发性铁粒幼细胞贫血中为17%,伴有过多原粒细胞的难治性贫血中为33%,3例单纯难治性贫血中为100%。这些异常是无系统性的。然而,有1例存在文献中已描述且被认为具有特异性的异常:5号染色体长臂缺失。在伴有过多原粒细胞的难治性贫血中,核型异常的患者(4/5)转化为急性白血病的情况似乎比核型正常的患者(0/10)更为常见。