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一例伴有8号与21号染色体易位以及Y染色体缺失(可能为继发事件)的急性单核细胞白血病。

A case of AMMoL with 8/21 translocation and loss of the Y as probably secondary events.

作者信息

Hustinx T W, Burghouts J T, Scheres J M, Smits A P

出版信息

Cancer. 1980 Jan 15;45(2):285-8. doi: 10.1002/1097-0142(19800115)45:2<285::aid-cncr2820450214>3.0.co;2-6.

Abstract

The clinical, hematological, and cytogenetic characteristics of a male patient with AMMoL are described. Before treatment a clone with the complex karyotype 45,X,del(7)(q32), t(8;21)(q22;q22) was present in the bone marrow. During partial remission induced by cytostatics, the percentage of normal cells increased, and a cell line having a 46,XY,del(7)(q32) karyotype was found. After four therapy courses, when remission was complete, only chromosomally normal cells were seen. The cytogenetic data suggest that in this case the 8/21 translocation and loss of the Y chromosome were only secondary events.

摘要

描述了一名急性单核细胞白血病男性患者的临床、血液学和细胞遗传学特征。治疗前,骨髓中存在复杂核型为45,X,del(7)(q32), t(8;21)(q22;q22)的克隆。在细胞抑制剂诱导的部分缓解期间,正常细胞百分比增加,并发现了核型为46,XY,del(7)(q32)的细胞系。四个疗程治疗后,当完全缓解时,仅见染色体正常的细胞。细胞遗传学数据表明,在该病例中,8号与21号染色体易位及Y染色体丢失只是继发事件。

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