On thorotrast leucaemia. Evolution of clone of bone marrow cells with radiation-induced chromosome aberrations.

J. Visfeldt, G. Jensen, E. Hippe
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引用次数: 3

Abstract

Results are presented of chromosome studies of bone marrow cells from a 62-year-old woman. The patient had been given 40 ml of Thorotrast in connection with a neuro-radiological examination 34 years earlier. Clinically, the patient was now considered to be in an incipient myeloid leucaemic phase. Ninety-seven per cent of the bone marrow cells belonged to a clone with characteristic marker chromosomes induced by radiation. Few data are available on chromosome analysis of bone marrow cells from Thorotrast patients. Therefore, the results of the present study are compared with data from chromosome analyses of 32P-treated patients with polycythaemia vera, in whom large clones were found in the bone marrow. The results of chromosome analysis of bone marrow cells from the Thorotrast patient support previous hypotheses concerning the carcinogenesis in radiation-induced leucaemia in patients with polycythaemia vera, treated with 32P. In the latter patients, the clone cells are pressumed to represent cell populations with selective qualities, originating from radiation-damaged cells, which possibly possess an increased tendency to malignant transformation because of a more pronounced sensitivity to carcinogenic agents. The cells might also be potentially malignant and manifest themselves as leucaemic cells, if the patient's immunological defence mechanism is broken.
关于乳房造影白血病。辐射诱导染色体畸变骨髓细胞克隆的进化。
结果提出了染色体研究的骨髓细胞从一个62岁的妇女。该患者在34年前的一次神经影像学检查中接受了40毫升的胸腔造影。临床上,该患者被认为处于早期髓性白血病期。97%的骨髓细胞属于由辐射诱导的具有特征标记染色体的克隆。关于胸腔造影患者骨髓细胞染色体分析的资料很少。因此,本研究的结果与32p治疗的真性红细胞增多症患者的染色体分析数据进行了比较,后者在骨髓中发现了大克隆。Thorotrast患者骨髓细胞的染色体分析结果支持先前的假设,即32P治疗真性红细胞增多症患者放射诱导白血病的致癌作用。在后一种患者中,克隆细胞被认为代表了具有选择性质的细胞群,起源于辐射损伤的细胞,由于对致癌物更明显的敏感性,这些细胞可能具有更大的恶性转化倾向。如果病人的免疫防御机制被破坏,这些细胞也可能是潜在的恶性细胞,表现为白血病细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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