Rolović Z, Cirić M, Mijović A
Cancer Genet Cytogenet. 1983 Jan;8(1):75-9. doi: 10.1016/0165-4608(83)90066-3.
A case of chronic myeloid leukemia (CML) with a short survival (11 months) is described. Cytogenetic peculiarities of the bone marrow cells analyzed by G-banding consisted of a Ph1 chromosome with no translocation and a translocation t(5;13). Hematological characteristics were marked leukocytosis and massive splenomegaly. After treatment with busulfan complete hematological remission was achieved, followed by the appearance of a normal clone. However, 6 months later the patient entered the blastic crisis and a hyperdiploid clone appeared. The usual chemotherapy was given, but the patient responded only partially and died with a prevalence of pathologic myeloblasts in the bone marrow, corresponding to progression of the hyperdiploid clone.
描述了一例慢性髓性白血病(CML)患者,其生存期较短(11个月)。通过G显带分析的骨髓细胞的细胞遗传学特征包括一条无易位的Ph1染色体和一个t(5;13)易位。血液学特征为显著的白细胞增多和巨大脾肿大。用白消安治疗后实现了完全血液学缓解,随后出现了一个正常克隆。然而,6个月后患者进入急变期,出现了一个超二倍体克隆。给予了常规化疗,但患者仅部分缓解,最终因骨髓中病理性成髓细胞占优势而死亡,这与超二倍体克隆的进展一致。