Selvaggi S, Wolman S R, Bornstein S, Edinger F
Cancer. 1984 Dec 15;54(12):2956-8. doi: 10.1002/1097-0142(19841215)54:12<2956::aid-cncr2820541224>3.0.co;2-h.
The clonal growth pattern of bone marrow and peripheral blood cells from 16 patients with clinically suspected chronic myelogenous leukemia (CML) was evaluated in the double-layer agar system. Cytogenetic studies were performed on parallel marrow and peripheral blood samples. In four cases a unique growth pattern emerged, characterized by normal or increased colony-forming units (CFUc), and markedly elevated cluster-forming units (CIFUc). Three of these were Philadelphia chromosome (Ph1)-negative (atypical CML) and the fourth showed a mixture of Ph1-positive and chromosomally normal cells (Ph1-negative). Of the remaining cases, five proved to be CML Ph1-positive with progression to blast crisis on the basis of clinical data, clonal culture, and cytogenetics, and seven proved to be disorders other than myeloid leukemia. The combined results from clonal growth and cytogenetics have added a new parameter in the diagnosis of atypical CML and may aid in the earlier diagnosis and treatment of patients with this CML variant.
在双层琼脂系统中评估了16例临床疑似慢性粒细胞白血病(CML)患者骨髓和外周血细胞的克隆生长模式。对平行的骨髓和外周血样本进行了细胞遗传学研究。在4例患者中出现了独特的生长模式,其特征为集落形成单位(CFUc)正常或增加,而集簇形成单位(CIFUc)显著升高。其中3例费城染色体(Ph1)阴性(非典型CML),第4例显示Ph1阳性细胞和染色体正常细胞的混合(Ph1阴性)。在其余病例中,根据临床数据、克隆培养和细胞遗传学,5例被证实为Ph1阳性的CML并进展为急变期,7例被证实为非髓系白血病的其他疾病。克隆生长和细胞遗传学的综合结果为非典型CML的诊断增加了一个新参数,可能有助于早期诊断和治疗这种CML变异型患者。