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首例急性髓系白血病(AML)患者异基因造血干细胞移植后二次发生新发 AML 的病例报告

A case report of the second de novo acute myeloid leukemia (AML) following allogeneic stem cell transplantation in a patient with the first AML.

机构信息

Division of Hematology, Department of Internal Medicine, Catholic Blood and Marrow Transplantation Center, The Catholic University of Korea School of Medicine, Seoul, Korea.

出版信息

Korean J Intern Med. 2010 Mar;25(1):110-3. doi: 10.3904/kjim.2010.25.1.110. Epub 2010 Feb 26.

Abstract

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.

摘要

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。

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