Division of Hematology, Department of Internal Medicine, Catholic Blood and Marrow Transplantation Center, The Catholic University of Korea School of Medicine, Seoul, Korea.
Korean J Intern Med. 2010 Mar;25(1):110-3. doi: 10.3904/kjim.2010.25.1.110. Epub 2010 Feb 26.
Secondary leukemia occurring after hematopoietic stem cell transplantation (HSCT) for acute myeloid leukemia (AML) is rare. Secondary AML usually follows autologous and not allogeneic transplants. When a new leukemia develops in a patient successfully treated with an allogeneic HSCT, the possibility of a de novo or secondary leukemia from either the donor or recipient should be considered. We present a case initially diagnosed as de novo AML without a cytogenetic abnormality. The patient was successfully treated with an HLA-matched sibling allogeneic HSCT. However, more than six years later, AML developed again and was associated with new complex cytogenetic abnormalities. After a second HSCT, the patient has been followed without serious complications. Considering the allogeneic setting, the newly developed cytogenetic abnormalities, a relatively long latent period, and the good clinical course after the second allogeneic HSCT, this case might represent a second de novo AML following successful treatment of the first AML.
异基因造血干细胞移植(HSCT)后发生的继发性白血病(AML)较为罕见。继发性 AML 通常发生于自体而非异基因移植后。当一位接受异基因 HSCT 成功治疗的患者出现新发白血病时,应考虑新发或来自供者或受者的继发性白血病的可能性。我们报告了一例最初诊断为无细胞遗传学异常的新发 AML 病例。该患者接受了 HLA 匹配的同胞异基因 HSCT 治疗,获得了成功。然而,6 年多后,AML 再次发生,伴有新的复杂细胞遗传学异常。在进行第二次 HSCT 后,患者未出现严重并发症。考虑到异基因背景、新出现的细胞遗传学异常、相对较长的潜伏期以及第二次异基因 HSCT 后的良好临床病程,本例可能代表在成功治疗首例 AML 后再次发生的新发 AML。