Watmore A E, Murray J A, Potter A M
Cancer Genet Cytogenet. 1985 Apr 15;16(4):283-8. doi: 10.1016/0165-4608(85)90234-1.
A long surviving patient with nonendemic Burkitt's lymphoma and complex cytogenetic findings is presented. Chromosome abnormalities were seen as a minor clone in peripheral blood and were considered consistent with the t(2;8)(p12;q24) variant. The karyotype was 47,XY, -2, -8, + der2(8qter-8q24::2p12-2qter), + der8(8pter-8q23::2p12-2pter) + der8(8qter-8cen::1q21-1qter). This case illustrates the value of extensive chromosome analysis in hematologic disorders and, at the time of writing, is the first example in Britain of the t(2;8) variant in Burkitt's lymphoma.
本文报告了一名长期存活的非地方性伯基特淋巴瘤患者,其具有复杂的细胞遗传学表现。外周血中可见染色体异常作为一个小克隆,被认为与t(2;8)(p12;q24)变异一致。核型为47,XY, -2, -8, + der2(8qter-8q24::2p12-2qter), + der8(8pter-8q23::2p12-2pter) + der8(8qter-8cen::1q21-1qter)。该病例说明了广泛染色体分析在血液系统疾病中的价值,并且在撰写本文时,是英国伯基特淋巴瘤中t(2;8)变异的首个病例。