Sibling donor-derived myeloid sarcoma after hematopoietic stem cell transplant

Q4 Medicine
Janelle Otsuji, Nicole Girard , Catherine Spier, Deborah Fuchs, Li-Wen Lai
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引用次数: 2

Abstract

Donor-derived myeloid sarcoma (DDMS) is a rare complication which occurs when donor stem cells undergo leukemic transformation. We report here two cases of DDMS following successful allogenic hematopoietic stem cell transplant (allo-HSCT) from HLA-identical, sex-mismatched sibling donors. Both were males in their fourth decade of life and originally diagnosed in 2012 with acute myeloid leukemia (AML) with t(6;11)(q27;q23) and AML with myelodysplasia-related changes (AML-MRC), respectively. They went onto allo-HSCT from their respective haploidentical sisters as donors and achieved complete engraftment in 2014. Both were in remission until 2019 when they were diagnosed with clinical relapse of AML in the setting of DDMS, one presenting in bilateral tibiae and the other in the testis. Verifying donor origin in AML relapse is critical as transformed donor cells may have different genetic alterations and behaviors from initial AML. We reviewed the literature of donor derived myeloid sarcoma and discussed the pathogenesis of this rare late complication of HSCT.

造血干细胞移植后同胞供者来源的髓系肉瘤
供体源性髓系肉瘤(DDMS)是一种罕见的并发症,发生在供体干细胞发生白血病转化时。我们在此报告两例DDMS后成功移植同种异体造血干细胞(同种异体造血干细胞)从hla相同,性别不匹配的兄弟姐妹供体。两例患者均为40岁男性,最初于2012年诊断为急性髓性白血病(AML)伴t(6;11)(q27;q23)和AML伴骨髓增生异常相关改变(AML- mrc)。他们从各自的单倍体姐妹身上获得同种异体造血干细胞作为供体,并于2014年实现了完全移植。两人在2019年之前都处于缓解期,当时他们被诊断为DDMS背景下的AML临床复发,一个出现在双侧胫骨,另一个出现在睾丸。在AML复发中验证供体来源至关重要,因为转化的供体细胞可能具有与初始AML不同的遗传改变和行为。我们回顾了供体源性髓系肉瘤的文献,并讨论了这种罕见的HSCT晚期并发症的发病机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Human Pathology: Case Reports
Human Pathology: Case Reports Medicine-Pathology and Forensic Medicine
CiteScore
0.50
自引率
0.00%
发文量
0
审稿时长
16 weeks
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