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具有生育能力的特纳综合征嵌合体(45,X/46,XX)的单体细胞系中的慢性粒细胞白血病

Chronic myelogenous leukemia in the monosomic cell line of a fertile Turner syndrome mosaic (45,X/46,XX).

作者信息

Chaganti R S, Bailey R B, Jhanwar S C, Arlin Z A, Clarkson B D

出版信息

Cancer Genet Cytogenet. 1982 Mar;5(3):215-21. doi: 10.1016/0165-4608(82)90027-9.

Abstract

Malignancy in patients with constitutional chromosome abnormality is of interest not only because it permits insights into the relationship between the chromosome abnormality and cancer, but also because it provides opportunities to address such questions as the clonality and evolution of tumors. We report Ph1-positive chronic myelogenous leukemia (CML) in a 50-year-old mosaic (45,X/46,XX) Turner syndrome patient whose leukemia was restricted to the monosomic cell line. Our extensive cytogenetic studies of this patient demonstrated that non-leukemic normal cells persisted in the marrow and were able to proliferate during a period of temporary suppression of the leukemic clone following aggressive treatment.

摘要

患有先天性染色体异常的患者发生恶性肿瘤不仅因为它有助于深入了解染色体异常与癌症之间的关系,还因为它为解决诸如肿瘤的克隆性和进化等问题提供了机会。我们报告了一名50岁的嵌合型(45,X/46,XX)特纳综合征患者发生的Ph1阳性慢性粒细胞白血病(CML),其白血病仅限于单体细胞系。我们对该患者进行的广泛细胞遗传学研究表明,非白血病正常细胞在骨髓中持续存在,并且在积极治疗后白血病克隆暂时受到抑制的期间能够增殖。

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