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一例伴有5号染色体长臂缺失(5q-)的造血发育异常病例中克隆进化的细胞遗传学证据

Cytogenetic evidence of clonal evolution in a case of hemopoietic dysplasia with a 5q- chromosome.

作者信息

Taniwaki M, Edagawa J, Sonoda Y, Nishida K, Misawa S, Abe T, Takino T, Arizono N

出版信息

Cancer Genet Cytogenet. 1983 Sep;10(1):59-65. doi: 10.1016/0165-4608(83)90106-1.

DOI:10.1016/0165-4608(83)90106-1
PMID:6883300
Abstract

A 70-year-old Japanese male with hemopoietic dysplasia is described. Cytogenetic investigation revealed an abnormal karyotype, 46,XY,del(5)(q13q33), in all metaphases examined at the time of diagnosis. Eight months later, a newly appearing abnormal hyperdiploid karyotype, 47,XY,5q-, +21, was observed in 74% of the cells analyzed, which was associated with evolution of the disease when a pathologic diagnosis of a myeloproliferative disorder was made.

摘要

本文描述了一名患有造血发育异常的70岁日本男性。细胞遗传学检查显示,在诊断时所检查的所有中期分裂相中,核型异常为46,XY,del(5)(q13q33)。8个月后,在分析的74%的细胞中观察到一种新出现的异常超二倍体核型47,XY,5q-, +21,在做出骨髓增殖性疾病的病理诊断时,这与疾病进展相关。

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