Milton J M, Garson O M, Paton C M, Hurley T F
Cancer Genet Cytogenet. 1984 Sep;13(1):37-41. doi: 10.1016/0165-4608(84)90086-4.
A patient with preleukemia who possessed a complicated hypodiploid karyotype in 100% of bone marrow cells is described. The clinical, hematologic, and cytogenetic features showed a marked similarity to a patient with preleukemia described by Watt et al. [1]. Both patients terminated their disease in acute nonlymphocytic leukemia. Another patient with similar cytogenetic features, but who presented in the acute leukemic phase of polycythemia rubra vera, also is described. All three patients possessed a translocation involving chromosome #11 at band p15. This, together with many numerical and structural abnormalities, particularly those involving chromosomes #5, #7, and #17, may prove useful in defining a variety of preleukemia with a poor prognosis.
本文描述了一名骨髓细胞100%具有复杂亚二倍体核型的白血病前期患者。其临床、血液学和细胞遗传学特征与Watt等人[1]描述的一名白血病前期患者极为相似。两名患者均发展为急性非淋巴细胞白血病。本文还描述了另一名具有相似细胞遗传学特征、但表现为真性红细胞增多症急性白血病期的患者。所有三名患者均存在涉及11号染色体p15带的易位。这一情况,连同许多数量和结构异常,尤其是涉及5号、7号和17号染色体的异常,可能有助于定义预后不良的各种白血病前期。