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与t(8;21)急性髓系白血病相关的系统性肥大细胞增多症中的肿瘤性肥大细胞源自白血病克隆。

Neoplastic mast cells in systemic mastocytosis associated with t(8;21) acute myeloid leukemia are derived from the leukemic clone.

作者信息

Pullarkat Vinod, Bedell Victoria, Kim Young, Bhatia Ravi, Nakamura Ryotaro, Forman Stephen, Sun Jiyao, Senitzer David, Slovak Marilyn L

机构信息

Division of Hematology and Hematopoietic Cell Transplantation, Department of Cytogenetics, Division of Pathology, City of Hope Comprehensive Cancer Center, 1500 East Duarte Road, Duarte, CA 91010, United States.

出版信息

Leuk Res. 2007 Feb;31(2):261-5. doi: 10.1016/j.leukres.2006.03.006. Epub 2006 Jul 28.

Abstract

In systemic mastocytosis with associated clonal, hematological non-mast cell lineage disease (SM-AHNMD), mast cell infiltration of the bone marrow coexists with a hematologic neoplasm, usually of myeloid origin. Activating KIT gene mutations are universally present in these neoplastic mast cells. When SM is associated with AML, the leukemic cells commonly carry the t(8;21)(q22;q22) core binding factor translocation. The precise relationship between neoplastic mast cells and the leukemic clone has remained unclear. By target FISH analysis, we demonstrate t(8;21) in the bone marrow mast cells of a patient with systemic mastocytosis associated with t(8;21) AML, thus, proving the origin of these neoplastic mast cells from the leukemic clone. We also show that after successful allogeneic hematopoietic stem cell transplantation, these neoplastic bone marrow mast cells can persist without adverse consequences and gradually decline with time.

摘要

在伴有相关克隆性血液非肥大细胞谱系疾病的系统性肥大细胞增多症(SM-AHNMD)中,骨髓中的肥大细胞浸润与血液系统肿瘤同时存在,该肿瘤通常起源于髓系。这些肿瘤性肥大细胞普遍存在激活的KIT基因突变。当SM与急性髓系白血病(AML)相关时,白血病细胞通常携带t(8;21)(q22;q22)核心结合因子易位。肿瘤性肥大细胞与白血病克隆之间的确切关系仍不清楚。通过靶向荧光原位杂交(FISH)分析,我们在一名患有与t(8;21) AML相关的系统性肥大细胞增多症患者的骨髓肥大细胞中证实了t(8;21),从而证明这些肿瘤性肥大细胞起源于白血病克隆。我们还表明,在成功进行异基因造血干细胞移植后,这些肿瘤性骨髓肥大细胞可以持续存在而无不良后果,并随时间逐渐减少。

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