Campbell M, Cabrera M E, Legues M E, Ridge S, Greaves M
Hospital Roberto del Rio, Santiago, Chile.
Br J Haematol. 1996 Apr;93(1):166-9. doi: 10.1046/j.1365-2141.1996.455999.x.
We report the different presentation features and clinical outcome between two identical infant twins with acute lymphoblastic leukaemia with a shared clonal disease and MLL gene rearrangement. One twin relapsed and died, but the other is in complete remission > 4 years after diagnosis. These data, and similar observations on other twin infants with leukaemia, suggest that despite a common clonal in utero, post-natally these leukaemias can evolve independently, at different rates, in the twinned individuals, and that the usually fatal leukaemia associated with t(4;11) MLL gene rearrangement can be effectively treated when the leukaemic burden is small.
我们报告了一对患有急性淋巴细胞白血病且具有共同克隆性疾病和MLL基因重排的同卵双胞胎婴儿的不同表现特征和临床结局。其中一个双胞胎复发并死亡,但另一个在诊断后4年多仍处于完全缓解状态。这些数据以及对其他白血病双胞胎婴儿的类似观察结果表明,尽管在子宫内存在共同克隆,但出生后这些白血病在双胞胎个体中可以以不同的速率独立演变,并且当白血病负担较小时,与t(4;11) MLL基因重排相关的通常致命的白血病可以得到有效治疗。