Jeong Seong Hyun, Han Jae Ho, Jeong Seon Yong, Kang Seok Yun, Lee Hyun Woo, Choi Jin-Hyuk, Park Joon Seong
Department of Hematology-Oncology, Ajou University School of Medicine, Suwon, Korea.
Korean J Hematol. 2010 Mar;45(1):70-2. doi: 10.5045/kjh.2010.45.1.70. Epub 2010 Mar 31.
The occurrence of granulocytic sarcoma as a pattern of relapse after allogeneic hematopoietic stem cell transplantation (allo-HSCT) is rare. In this paper, we report a rare case of acute myeloid leukemia (AML) relapsed as a granulocytic sarcoma of the donor type. The patient was diagnosed as having AML and underwent an allo-HSCT from his matched sibling donor. Fifty-seven months after allo-HSCT, he developed granulocytic sarcomas of duodenum, jejunum, and left sterno-cleido-mastoid muscle. The bone marrow was normal with 100% donor chimerism. A Y chromosome PCR was performed on the patient's duodenum specimen as well as bone marrow aspirate in order to check the patient-origin cells. The duodenal specimen was found to contain 41.2% SRY-positive cells (from the donor). Repeat endoscopy on day 2 of chemotherapy showed that the granulocytic sarcoma had shrunk dramatically. The patient died of sepsis during the nadir state 35 days after starting salvage chemotherapy.
异基因造血干细胞移植(allo-HSCT)后以粒细胞肉瘤形式复发的情况较为罕见。在本文中,我们报告了一例罕见的急性髓系白血病(AML)复发为供者型粒细胞肉瘤的病例。该患者被诊断为AML,并接受了来自其匹配同胞供者的allo-HSCT。allo-HSCT后57个月,他出现了十二指肠、空肠和左胸锁乳突肌的粒细胞肉瘤。骨髓正常,供者嵌合率为100%。对患者的十二指肠标本以及骨髓穿刺液进行了Y染色体PCR检测,以检查患者来源的细胞。发现十二指肠标本中含有41.2%的SRY阳性细胞(来自供者)。化疗第2天重复内镜检查显示粒细胞肉瘤显著缩小。患者在开始挽救化疗35天后的最低点状态时死于败血症。