• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

白血病中的血小板减少症:发病机制与预后

Thrombocytopenia in leukemia: Pathogenesis and prognosis.

作者信息

Shahrabi Saeid, Behzad Masumeh Maleki, Jaseb Kaveh, Saki Najmaldin

机构信息

Department of Biochemistry and Hematology, Faculty of Medicine, Semnan University of Medical Sciences, Semnan, Iran.

Research Center of Thalassemia and Hemoglobinopathy, Health Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.

出版信息

Histol Histopathol. 2018 Sep;33(9):895-908. doi: 10.14670/HH-11-976. Epub 2018 Feb 20.

DOI:10.14670/HH-11-976
PMID:29460950
Abstract

Leukemias, a heterogeneous group of hematological disorders, are characterized by ineffective hematopoiesis and morphologic abnormalities of hematopoietic cells. Thrombocytopenia is a common problem among leukemia types that can lead to hemorrhagic complications in patients. The purpose of this review article is to identify the conditions associated with the incidence of thrombocytopenia in leukemias. It can be stated that although translocations have been considered responsible for this complication in many studies, other factors such as bone marrow failure, genes polymorphism, a mutation in some transcription factors, and the adverse effects of treatment could be associated with pathogenesis and poor prognosis of thrombocytopenia in leukemias. Considering the importance of thrombocytopenia in leukemias, it is hoped that the recognition of risk factors increasing the incidence of this complication in leukemic patients would be useful for prevention and treatment of this disorder.

摘要

白血病是一组异质性血液系统疾病,其特征为造血功能无效及造血细胞形态异常。血小板减少是白血病类型中常见的问题,可导致患者出现出血并发症。这篇综述文章的目的是确定与白血病患者血小板减少发生率相关的情况。可以说,尽管在许多研究中易位被认为是导致这种并发症的原因,但其他因素,如骨髓衰竭、基因多态性、某些转录因子的突变以及治疗的不良反应,可能与白血病患者血小板减少的发病机制和不良预后有关。鉴于血小板减少在白血病中的重要性,希望识别增加白血病患者这种并发症发生率的危险因素将有助于预防和治疗这种疾病。

相似文献

1
Thrombocytopenia in leukemia: Pathogenesis and prognosis.白血病中的血小板减少症:发病机制与预后
Histol Histopathol. 2018 Sep;33(9):895-908. doi: 10.14670/HH-11-976. Epub 2018 Feb 20.
2
[Role of TEL gene alterations in childhood leukemias].[TEL基因改变在儿童白血病中的作用]
Rinsho Ketsueki. 2011 Aug;52(8):686-94.
3
RUNX1-EVI1 induces dysplastic hematopoiesis and acute leukemia of the megakaryocytic lineage in mice.RUNX1-EVI1可诱导小鼠巨核细胞系发育异常造血及急性白血病。
Leuk Res. 2018 Nov;74:14-20. doi: 10.1016/j.leukres.2018.09.015. Epub 2018 Sep 26.
4
Hereditary thrombocytopenias: a growing list of disorders.遗传性血小板减少症:不断增加的疾病种类。
Hematology Am Soc Hematol Educ Program. 2017 Dec 8;2017(1):385-399. doi: 10.1182/asheducation-2017.1.385.
5
Adult acute leukemia.成人急性白血病。
Dis Mon. 2012 Apr;58(4):219-38. doi: 10.1016/j.disamonth.2012.01.011.
6
The AML1 gene: a transcription factor involved in the pathogenesis of myeloid and lymphoid leukemias.AML1基因:一种参与髓系和淋巴系白血病发病机制的转录因子。
Haematologica. 1997 May-Jun;82(3):364-70.
7
Alterations of the AML1 transcription factor in human leukemia.人类白血病中AML1转录因子的改变。
Semin Cell Dev Biol. 2000 Oct;11(5):347-60. doi: 10.1006/scdb.2000.0183.
8
Core-binding factor: a central player in hematopoiesis and leukemia.核心结合因子:造血作用和白血病中的关键因子
Cancer Res. 1999 Apr 1;59(7 Suppl):1789s-1793s.
9
ETV6-related thrombocytopenia and leukemia predisposition.ETV6 相关血小板减少症和白血病易感性。
Blood. 2019 Aug 22;134(8):663-667. doi: 10.1182/blood.2019852418. Epub 2019 Jun 27.
10
A Rare Case of ETV6/MECOM Rearrangement in Therapy-Related Acute Myeloid Leukemia with t(3;12) and Monosomy 7.伴有t(3;12)和7号染色体单体的治疗相关急性髓系白血病中ETV6/MECOM重排的罕见病例
Clin Lab. 2017 Feb 1;63(2):415-418. doi: 10.7754/Clin.Lab.2016.160815.

引用本文的文献

1
Development of Nomogram for Predicting the Overall Survival of Diffuse Large B-Cell Lymphoma (DLBCL) Patients Based on Clinical Data and Systemic Inflammation Markers.基于临床数据和全身炎症标志物的弥漫性大B细胞淋巴瘤(DLBCL)患者总生存预测列线图的开发
Asian Pac J Cancer Prev. 2025 Jun 1;26(6):2145-2154. doi: 10.31557/APJCP.2025.26.6.2145.
2
Multitarget Mechanisms of Monocarbonyl Curcuminoid Analogues against HL-60 Cancer Cells: and Network Pharmacology-Based Approach.单羰基姜黄素类似物抗HL-60癌细胞的多靶点机制:基于网络药理学的方法
ACS Omega. 2024 Feb 27;9(10):11836-11847. doi: 10.1021/acsomega.3c09427. eCollection 2024 Mar 12.
3
Effectiveness and economic evaluation of rhTPO and rhIL-11 in the treatment of cancer therapy induced thrombocytopenia based on real-world research.
基于真实世界研究的重组人血小板生成素和重组人白细胞介素-11治疗癌症治疗所致血小板减少症的有效性及经济学评价
Front Pharmacol. 2024 Jan 23;15:1288964. doi: 10.3389/fphar.2024.1288964. eCollection 2024.
4
Identification of novel clusters of co-expressing cytokines in a diagnostic cytokine multiplex test.鉴定诊断性细胞因子多重检测中新型共表达细胞因子簇。
Front Immunol. 2023 Jul 31;14:1223817. doi: 10.3389/fimmu.2023.1223817. eCollection 2023.
5
Excessive serine from the bone marrow microenvironment impairs megakaryopoiesis and thrombopoiesis in Multiple Myeloma.骨髓微环境中过多的丝氨酸会损害多发性骨髓瘤中的巨核细胞生成和血小板生成。
Nat Commun. 2023 Apr 13;14(1):2093. doi: 10.1038/s41467-023-37699-z.
6
Advances in the application of Raman spectroscopy in haematological tumours.拉曼光谱在血液系统肿瘤中的应用进展
Front Bioeng Biotechnol. 2023 Jan 10;10:1103785. doi: 10.3389/fbioe.2022.1103785. eCollection 2022.
7
Dynamic trajectory of platelet counts after the first cycle of induction chemotherapy in AML patients.急性髓细胞白血病患者诱导化疗第一周期后血小板计数的动态轨迹。
BMC Cancer. 2022 May 1;22(1):477. doi: 10.1186/s12885-022-09601-5.
8
Ecchymosis: A Subtle Sign Unmasking Malignancy.瘀斑:揭示恶性肿瘤的微妙迹象。
Indian Dermatol Online J. 2022 Mar 3;13(2):262-265. doi: 10.4103/idoj.idoj_388_21. eCollection 2022 Mar-Apr.
9
Leukapheresis and Hyperleukocytosis, Past and Future.白细胞去除术与高白细胞血症:过去与未来
Int J Gen Med. 2021 Jul 14;14:3457-3467. doi: 10.2147/IJGM.S321787. eCollection 2021.
10
CD markers polymorphisms as prognostic biomarkers in hematological malignancies.CD标志物多态性作为血液系统恶性肿瘤的预后生物标志物
Oncol Rev. 2020 Jul 14;14(2):466. doi: 10.4081/oncol.2020.466. eCollection 2020 Jul 6.