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急性淋巴细胞白血病中涉及9号染色体短臂和/或12号染色体短臂的易位。英国癌症细胞遗传学小组(UKCCG)。

Translocations involving 9p and/or 12p in acute lymphoblastic leukemia. United Kingdom Cancer Cytogenetics Group (UKCCG).

出版信息

Genes Chromosomes Cancer. 1992 Oct;5(3):255-9. doi: 10.1002/gcc.2870050314.

Abstract

Fifteen cases of acute lymphoblastic leukemia (ALL) with translocations involving 9p and/or 12p are described. Four children, three males and one female, age range 1-8 yrs, had translocations involving 9p but not 12p. Of these, three had B-lineage ALL and one had biphenotypic T-ALL/acute myeloid leukemia. Six patients, three males and three females, age range 1-49 yrs, had translocations involving 12p but not 9p. Five had B-lineage ALL and one had T-ALL. One patient had dic(7;12)(p11;p11), confirming that this previously reported translocation is nonrandom in ALL. One patient had t(2;12)(q14;p13), and it is suggested that this may also be a new nonrandom abnormality. Five patients, four males and one female, age range 11-21 yrs, had common ALL and dic(9;12). The dic(9;12) appears to confer a better prognosis than do other translocations involving 9p or 12p.

摘要

本文描述了15例伴有9号染色体短臂(9p)和/或12号染色体短臂(12p)易位的急性淋巴细胞白血病(ALL)病例。4名儿童(3名男性,1名女性),年龄在1至8岁之间,发生了涉及9p但不涉及12p的易位。其中,3例为B系ALL,1例为双表型T-ALL/急性髓系白血病。6例患者(3名男性,3名女性),年龄在1至49岁之间,发生了涉及12p但不涉及9p的易位。5例为B系ALL,1例为T-ALL。1例患者有双着丝粒染色体(7;12)(p11;p11),证实这种先前报道的易位在ALL中并非随机发生。1例患者有t(2;12)(q14;p13),提示这可能也是一种新的非随机异常。5例患者(4名男性,1名女性),年龄在11至21岁之间,患有普通ALL和双着丝粒染色体(9;12)。双着丝粒染色体(9;12)似乎比其他涉及9p或12p的易位预后更好。

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