Bennett D D, Stanley W S, Johnson C B
Acta Haematol. 1985;73(4):235-8. doi: 10.1159/000206336.
Bone marrow from an 81-year-old male with acquired idiopathic sideroblastic anemia was found to be mosaic for 45,X/46,XY cell lines. Analysis of ringed sideroblasts for the presence or absence of a quinicrine fluorescent Y body indicated that all sideroblastic cells had lost the Y chromosome. The demonstration that the ringed sideroblasts were cytogenetically abnormal in this patient provides evidence that the cytogenetic changes often found in patients with sideroblastic anemia may not be due to randomly acquired chromosome aberrations accompanying tissue aging unrelated to the disease process.
一名81岁患有获得性特发性铁粒幼细胞贫血男性的骨髓被发现存在45,X/46,XY细胞系的嵌合体。对环形铁粒幼细胞进行奎纳克林荧光Y小体有无的分析表明,所有铁粒幼细胞均丢失了Y染色体。该患者环形铁粒幼细胞存在细胞遗传学异常的证明提供了证据,表明铁粒幼细胞贫血患者中常见的细胞遗传学改变可能并非由于与疾病过程无关的组织衰老随机获得的染色体畸变所致。