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急性骨髓纤维化、骨髓增生异常综合征和急性非淋巴细胞白血病中出现的易位t(6;9)提示多能干细胞受累。

Translocation t(6;9) occurring in acute myelofibrosis, myelodysplastic syndrome, and acute nonlymphocytic leukemia suggests multipotent stem cell involvement.

作者信息

Cuneo A, Kerim S, Vandenberghe E, Van Orshoven A, Rodhain J, Bosly A, Zachee P, Louwagie A, Michaux J L, Dal Cin P

机构信息

Centre for Human Genetics, University of Leuven, Belgium.

出版信息

Cancer Genet Cytogenet. 1989 Oct 15;42(2):209-19. doi: 10.1016/0165-4608(89)90089-7.

Abstract

The cytological and cytogenetic features of six patients with myeloid neoplasia and t(6;9)(p23;q34) including a case of acute myelofibrosis (AMF), a refractory anemia with excess of blasts (RAEB), and four cases of acute nonlymphocytic leukemia (ANLL) are described. Two patients in this series, both affected by ANLL type M2, presented an increase of bone marrow basophils, suggesting that this cytological-cytogenetic association is not absolute and that it may be more frequently observed in ANLL with maturation. All patients with de novo ANLL showed associated myelodysplastic features, and one patient presented a dysmyelopoietic syndrome, later evolving into ANLL. The presence of the t(6;9) in a range of myeloid neoplasias, with either concurrent myelodysplastic features or a preleukemic phase in cases of ANLL, provide evidence that this chromosome aberration may always involve a multipotent myeloid stem cell. Data on toxic exposure of the patients suggests that myeloproliferative disorders with the t(6;9) may frequently represent environmentally induced neoplasias.

摘要

描述了6例患有骨髓肿瘤且伴有t(6;9)(p23;q34)的患者的细胞学和细胞遗传学特征,其中包括1例急性骨髓纤维化(AMF)、1例伴原始细胞增多的难治性贫血(RAEB)以及4例急性非淋巴细胞白血病(ANLL)。该系列中的2例患者均为M2型ANLL,其骨髓嗜碱性粒细胞增多,这表明这种细胞学-细胞遗传学关联并非绝对,且在有成熟现象的ANLL中可能更常见。所有新发ANLL患者均表现出相关的骨髓发育异常特征,1例患者出现骨髓造血异常综合征,随后发展为ANLL。在一系列骨髓肿瘤中存在t(6;9),在ANLL病例中伴有骨髓发育异常特征或白血病前期,这表明这种染色体畸变可能总是涉及多能骨髓干细胞。关于患者接触毒物的数据表明,伴有t(6;9)的骨髓增殖性疾病可能常为环境诱导的肿瘤。

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