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Donor cell-derived transient abnormal myelopoiesis as a specific complication of umbilical cord blood transplantation.

作者信息

Hiramoto N, Takeda J, Yoshida K, Ono Y, Yoshioka S, Yamauchi N, Fujimoto A, Maruoka H, Shiraishi Y, Tanaka H, Chiba K, Imai Y, Miyano S, Ogawa S, Ishikawa T

机构信息

Department of Cell Therapy, Institute of Biomedical Research and Innovation, Kobe, Japan.

Department of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

出版信息

Bone Marrow Transplant. 2018 Feb;53(2):225-227. doi: 10.1038/bmt.2017.226. Epub 2017 Oct 9.

DOI:10.1038/bmt.2017.226
PMID:28991249
Abstract
摘要

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Donor cell-derived transient abnormal myelopoiesis as a specific complication of umbilical cord blood transplantation.供体细胞衍生的短暂异常髓系造血作为脐带血移植的一种特殊并发症。
Bone Marrow Transplant. 2018 Feb;53(2):225-227. doi: 10.1038/bmt.2017.226. Epub 2017 Oct 9.
2
[Remark on donor cell-derived leukemia after umbilical blood cord transplantation--editorial].[关于脐血移植后供体细胞源性白血病的评论——编者按]
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Secondary leukaemia: after umbilical cord blood stem cell transplantation too.继发性白血病：同样也发生于脐带血干细胞移植后。
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Comparable long-term outcome of unrelated cord blood transplantation with related bone marrow or peripheral blood stem cell transplantation in patients aged 45 years or older with hematologic malignancies after myeloablative conditioning.45岁及以上血液系统恶性肿瘤患者在清髓性预处理后接受非亲缘脐血移植与亲缘骨髓或外周血干细胞移植的长期疗效比较。
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Clinical use of umbilical cord blood hematopoietic stem cells.脐带血造血干细胞的临床应用。
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Donor cell-derived myelodysplastic syndrome after cord blood transplantation.脐血移植后供体细胞来源的骨髓增生异常综合征
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Transplants of umbilical-cord blood or bone marrow from unrelated donors in adults with acute leukemia.成人急性白血病患者接受来自无关供者的脐带血或骨髓移植。
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Transient donor cell-derived myelodysplastic syndrome with monosomy 7 after unrelated cord blood transplantation.非亲缘脐血移植后出现的供体细胞来源的伴有7号染色体单体的短暂性骨髓增生异常综合征
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引用本文的文献

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Post-transplant transient abnormal myelopoiesis evolving from a GATA1 mutant clone in umbilical cord blood.移植后短暂异常髓系造血由脐带血中的GATA1突变克隆演变而来。
Ann Hematol. 2024 Dec;103(12):5989-5998. doi: 10.1007/s00277-024-06123-x. Epub 2024 Dec 12.

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Acute megakaryoblastic leukemia with acquired trisomy 21 and GATA1 mutations in phenotypically normal children.表型正常儿童中伴有获得性21号染色体三体和GATA1突变的急性巨核细胞白血病
Eur J Pediatr. 2015 Apr;174(4):525-31. doi: 10.1007/s00431-014-2430-3. Epub 2014 Sep 30.
2
Haematopoietic development and leukaemia in Down syndrome.唐氏综合征中的造血发育与白血病
Br J Haematol. 2014 Dec;167(5):587-99. doi: 10.1111/bjh.13096. Epub 2014 Aug 22.
3
Transient leukemia in a newborn without Down syndrome: case report and review of the literature.
一名无唐氏综合征新生儿的短暂性白血病：病例报告及文献综述
Eur J Pediatr. 2014 Dec;173(12):1643-7. doi: 10.1007/s00431-013-2163-8. Epub 2013 Nov 20.
4
The landscape of somatic mutations in Down syndrome-related myeloid disorders.唐氏综合征相关髓系疾病中体细胞突变的全景。
Nat Genet. 2013 Nov;45(11):1293-9. doi: 10.1038/ng.2759. Epub 2013 Sep 22.
5
GATA1-mutant clones are frequent and often unsuspected in babies with Down syndrome: identification of a population at risk of leukemia.GATA1 突变克隆在唐氏综合征婴儿中很常见且常常被忽视：白血病风险人群的鉴定。
Blood. 2013 Dec 5;122(24):3908-17. doi: 10.1182/blood-2013-07-515148. Epub 2013 Sep 10.
6
Exome sequencing identifies putative drivers of progression of transient myeloproliferative disorder to AMKL in infants with Down syndrome.外显子组测序鉴定出唐氏综合征婴儿短暂性髓系增生异常向急性髓系白血病进展的潜在驱动因素。
Blood. 2013 Jul 25;122(4):554-61. doi: 10.1182/blood-2013-03-491936. Epub 2013 Jun 3.
7
Natural history of transient myeloproliferative disorder clinically diagnosed in Down syndrome neonates: a report from the Children's Oncology Group Study A2971.Down 综合征新生儿临床诊断的短暂性髓系增生异常的自然病史：来自儿童肿瘤组研究 A2971 的报告。
Blood. 2011 Dec 22;118(26):6752-9; quiz 6996. doi: 10.1182/blood-2011-04-350017. Epub 2011 Aug 17.
8
Mosaic Down syndrome-associated acute myeloid leukemia does not require high-dose cytarabine treatment for induction and consolidation therapy.镶嵌型唐氏综合征相关急性髓系白血病在诱导和巩固治疗中并不需要高剂量阿糖胞苷治疗。
Int J Hematol. 2010 May;91(4):630-5. doi: 10.1007/s12185-010-0549-1. Epub 2010 Mar 18.
9
Abnormalities in the myeloid progenitor compartment in Down syndrome fetal liver precede acquisition of GATA1 mutations.唐氏综合征胎儿肝脏中髓系祖细胞区室的异常先于GATA1突变的获得。
Blood. 2008 Dec 1;112(12):4507-11. doi: 10.1182/blood-2008-04-152967. Epub 2008 Aug 8.
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Prospective study of a pirarubicin, intermediate-dose cytarabine, and etoposide regimen in children with Down syndrome and acute myeloid leukemia: the Japanese Childhood AML Cooperative Study Group.吡柔比星、中剂量阿糖胞苷和依托泊苷方案治疗唐氏综合征合并急性髓系白血病患儿的前瞻性研究：日本儿童急性髓系白血病协作研究组
J Clin Oncol. 2007 Dec 1;25(34):5442-7. doi: 10.1200/JCO.2007.12.3687.