日本原子弹幸存者的白血病前期状态。

N Kamada, H Uchino
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引用次数: 19

摘要

对长期患有血液病并急性白血病终止(第一组,6例)和未终止(第二组,6例)的原子弹暴露患者以及表面健康状况良好的幸存者(第三组,85例)的骨髓细胞进行了细胞学和细胞遗传学研究。除了一名在白血病前期接受检查的患者外,所有患者都有异常克隆。6例I组患者中有4例在白血病发生前3-10年出现骨髓细胞形态异常,如巨中性粒细胞或嗜碱性粒细胞、双核粒细胞或巨核细胞、中期染色单体桥状形成。II组患者均有稳定类型的染色体畸变。细胞学异常类型与ⅰ组相似,但频率略低于ⅰ组。ⅲ组有14例稳定型染色体畸变,其中11例有明显但短暂的克隆形成。本组未见细胞学及临床异常。长期血液病患者的细胞学和细胞遗传学异常的持续和高百分比,无论辐射暴露史如何,都提示白血病前期状态,也为白血病发生问题提供了一些线索。
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Preleukemic states in atomic bomb survivors in Japan.

Cytologic and cytogenetic studies were performed on the bone marrow cells in atomic bomb-exposed patients who had prolonged periods of blood disorders with termination of acute leukemia (group I, 6 cases) and without the termination (group II, 6 cases), and survivors who were in apparent good health (group III, 85 cases). All but one patient in group I, who were examined at the preleukemic state, had abnormal clones. In 4 out of 6 of group I patients, morphologic abnormalities of bone marrow cells taken 3-10 years before leukemic development were found, such as giant neutrophils or basophils, binucleated granulocytes or megakaryocytes, and bridge formation of chromatid in metaphases. All patients in group II had stable types of chromosome aberrations. The types of cytologic abnormalities were similar to those in group I, but the frequencies were a little less than those in group I. In group III, 14 persons were found to have stable types of chromosome aberrations, of which 11 persons had apparent but transient clone formations. Cytologic and clinical abnormalities were not observed in the group. The persistent and high percentages of cytologic and cytogenetic abnormalities in patients with prolonged periods of blood disorders, regardless of history of radiation exposure, would suggest a preleukemic state, and also give some clue to the problems of leukemogenesis.

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Cytochemical study of the cell colonies from agar culture of normal bone marrow and of peripheral blood from patients with chronic myeloid leukemia. [Study group on bone marrow insufficiency (proceedings)]. [Relapsing erythroblastopenia. A case followed during 22 years (author's transl)]. [Peripheral blood cell culture in myelosclerosis (author's transl)]. [Skeletal and medullary involvement in Hodgkin's disease].
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