Bowcock S J, Galton D A, Goldman J M
Department of Haematology, Royal Postgraduate Medical School, London, U.K.
Eur J Haematol. 1989 May;42(5):496-7. doi: 10.1111/j.1600-0609.1989.tb01477.x.
A 31-year-old woman with Philadelphia chromosome-positive chronic myeloid leukaemia (CML) was treated intermittently with high-dose busulphan over a 6-yr period (total dose 1320 mg). 3 yr later (after receiving no further cytotoxic drugs) she developed pancytopenia and marrow aplasia of relatively abrupt onset. Transfusion of reconstituted blood-derived stem cells (collected 7 yr previously) re-established chronic phase CML. These events are more consistent with 'stem cell exhaustion' than with an acquired marrow microenvironmental defect occurring in the course of CML. The contribution of busulphan is uncertain.
一名31岁费城染色体阳性慢性髓性白血病(CML)女性患者在6年期间间歇性接受大剂量白消安治疗(总剂量1320mg)。3年后(在未再接受细胞毒性药物治疗后),她出现全血细胞减少和相对急性起病的骨髓再生障碍。输注重构的血液来源干细胞(7年前采集)使慢性期CML得以重建。这些事件更符合“干细胞耗竭”,而非CML病程中发生的获得性骨髓微环境缺陷。白消安的作用尚不确定。