急性早幼粒细胞白血病缓解16年后腰椎髓外复发1例并文献复习。

IF 0.2 Q4 MEDICINE, RESEARCH & EXPERIMENTAL International journal of clinical and experimental medicine Pub Date : 2015-12-15 DOI:10.3760/CMA.J.ISSN.1671-7368.2016.01.018
Zheng-mei He, Shan-dong Tao, Yuan Deng, Yue Chen, Lixiao Song, Bang-he Ding, Kankan Chen, Liang Yu, Chun-ling Wang
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引用次数: 4

摘要

急性早幼粒细胞白血病(APL)是一种常见的髓系白血病。在新诊断阶段,它可能是致命的,因为严重的并发症-弥散性血管内凝血。随着全反式维甲酸的出现和早期应用,大多数APL患者可以获得长期生存,只有少数患者缓解后会出现髓外复发。髓外复发最常见的部位是中枢神经系统,其他部位相对少见。在这里,我们报告了一个特别罕见的APL患者,他经历了髓外复发,腰椎作为孤立部位,经过16年的相当长时间的缓解。复发时,患者的主要临床表现为明显的腰痛、下肢无力、活动受限。经局部放疗联合ATRA、三氧化二砷治疗,患者达到并维持第二次完全缓解。
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Extramedullary relapse in lumbar spine of patient with acute promyelocytic leukemia after remission for 16 years: a case report and literature review.
Acute promyelocytic leukemia (APL) is a common myeloid leukemia. At the newly diagnosed stage, it can be fatal because of the serious complication-disseminated intravascular coagulation. With the advent and early application of all-trans retinoic acid, most APL patients can achieve a long-term survival, and only a minority of patients will develop extramedullary relapse after remission. The most common site of extramedullary relapse is central nervous system, while other sites are relatively rare. Here, we report a particularly rare APL patient who experienced extramedullary relapse with lumbar spine as the isolated site after a rather long time of remission for 16 years. At the time of relapse, the main clinical manifestations of the patient are obvious low back pain, weakness in lower limbs and limitation of activity. After treatment of local radiotherapy combined with ATRA and arsenic trioxide, the patient achieved and maintained a second complete remission by now.
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