Thrombosis in Philadelphia negative classical myeloproliferative neoplasms: a narrative review on epidemiology, risk assessment, and pathophysiologic mechanisms

被引:17
作者
Ball, Somedeb [1 ,3 ]
Thein, Kyaw Zin [1 ]
Maiti, Abhishek [2 ]
Nugent, Kenneth [1 ]
机构
[1] Texas Tech Univ, Hlth Sci Ctr, 3601 4th St Stop 9410, Lubbock, TX 79430 USA
[2] Univ Texas MD Anderson Canc Ctr, 1515 Holcombe Blvd, Houston, TX 77030 USA
[3] Texas Tech Univ, Hlth Sci Ctr, Dept Internal Med, 3601 4th St Stop 9410, Lubbock, TX 79430 USA
关键词
Myeloproliferative neoplasm; Venous thromboembolism; Essential thrombocythemia; JAK2V617F mutation; Leukocyte activation; Microparticles; JAK2 V617F MUTATION; CIRCULATING ENDOTHELIAL-CELLS; EXTRACELLULAR DNA TRAPS; ESSENTIAL THROMBOCYTHEMIA; POLYCYTHEMIA-VERA; TISSUE FACTOR; PLATELET ACTIVATION; PROCOAGULANT MICROPARTICLES; VENOUS THROMBOEMBOLISM; LEUKOCYTE ACTIVATION;
D O I
10.1007/s11239-018-1623-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Thrombosis is common in cancer patients and is associated with increased morbidity and mortality. Myeloproliferative neoplasms (MPN) are common malignancies in elderly individuals and are known for a high incidence of thrombotic complications. Different risk factors have been identified in studies, and risk models have been developed to identify patients with MPN at higher risk for thrombosis. Several pathophysiological mechanisms help explain the increased likelihood of thrombosis in these patients. Factors, such as leukocyte and platelet activation leading to the formation of leukocyte-platelet aggregates, activation of the coagulation cascade by microparticles, high levels of inflammatory cytokines, and endothelial dysfunction have a crucial role in thrombosis in MPN patients. Recent studies have demonstrated a significant association between the allele burden of specific genetic mutations (mainly JAK2V617F) associated with MPN and the incidence of thrombotic events, thus suggesting a possible role for these mutations in thrombogenesis.
引用
收藏
页码:516 / 528
页数:13
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