Schafer A I
Department of Medicine, Baylor College of Medicine, Houston, Texas, USA.
Blood Rev. 2001 Dec;15(4):159-66. doi: 10.1054/blre.2001.0162.
Thrombocytosis is caused by three major pathophysiological mechanisms: (1) reactive or secondary thrombocytosis; (2) familial thrombocytosis; and (3) clonal thrombocytosis, including essential thrombocythemia and related myeloproliferative disorders. Recent work has begun to elucidate the abnormal megakaryocytopoiesis of essential thrombocythemia, which is associated with paradoxically elevated plasma levels of thrombopoietin. The clonal nature of all cases of essential thrombocythemia has been challenged. Thrombotic complications are the major causes of morbidity and mortality in this disease. Indications for platelet cytoreduction and antiplatelet therapy, as well as complications of treatment, are being clarified.
(1)反应性或继发性血小板增多症;(2)家族性血小板增多症;(3)克隆性血小板增多症,包括原发性血小板增多症及相关骨髓增殖性疾病。最近的研究已开始阐明原发性血小板增多症异常的巨核细胞生成,这与血小板生成素血浆水平反常升高有关。所有原发性血小板增多症病例的克隆性质都受到了质疑。血栓形成并发症是该疾病发病和死亡的主要原因。血小板细胞减少和抗血小板治疗的指征以及治疗并发症正在逐步明确。