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作 者:于亚平[1] 刘海宁[1] 翟勇平[1] 史平[1] 宋萍[1] 李峰[1] 周晓刚[1] 唐玉梅[1]
机构地区:[1]南京军区南京总医院血液科,江苏南京210002
出 处:《现代肿瘤医学》2011年第3期537-540,共4页Journal of Modern Oncology
摘 要:目的:探讨相关性急性早幼粒细胞白血病(t-APL)的临床特点和治疗。方法:报告1例滤泡型淋巴瘤治疗后的(t-APL),并复习相关文献。结果:1例38岁的滤泡型淋巴瘤患者共接受了20疗程的化疗,包括6疗程的FND(复达拉滨、米托蒽醌、地塞米松)方案。治疗56个月后,患者出现全血细胞减少,骨髓检查诊断为APL,染色体检查为t(15;17)(q22;q12)。在应用全反式维甲酸、亚砷酸和联合化疗治疗后,获完全缓解,但16个月死于淋巴瘤复发。结论:在以复达拉滨为基础的联合化疗方案治疗滤泡型淋巴瘤时,应考虑可能发生t-APL的危险,需密切监测血细胞变化。Objective:To describe the clinical characteristic of therapy-related acute promyelocytic leukemia(t-APL) following therapy for follicular lymphoma.Methods: One case of t-APL was reported and the literatures were reviewed.Results: A 38-year-old man with follicular leukemia received 20 cycles chemotherapy,which included 6 cycles of FND(fludarabine,mitoxantrone,and dexamethasone).After 56 months,he presented with pancytopenia.Marrow examination showed acute promyelocytic leukemia(APL) and cytogenetic analysis showed an balanced translocation t(15;17)(q22;q12).He achieved molecular remission after treatment of all-trans retinoic acid,arsenic acid and combined chemotherapy,and died from relapse of follicular lymphoma after 16 months of complete remission of APL.Conclusion: When decision is made to treat follicular lymphoma with fludarabinea-based combination chemotherapy protocols,potential risk for t-APL should be considered and a close clinical and laboratory monitoring is warranted.
关 键 词:急性早幼粒细胞白血病 治疗相关性 滤泡型淋巴瘤 复达拉滨
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