Kessler C M, Klein H G, Havlik R J
Br J Haematol. 1982 Jan;50(1):157-67. doi: 10.1111/j.1365-2141.1982.tb01900.x.
A retrospective study was performed to examine the natural course of uncontrolled thrombocytosis associated with chronic myeloproliferative disorders. Thirty-eight patients with polycythaemia rubra vera (PV), myelofibrosis/myeloid metaplasia (MM), chronic myelogenous leukaemia (CML) or essential thrombocythaemia (ET) had platelet counts greater than 1000 X 10(9)/1 and were followed closely for a total of 246 patient years. Eleven of the patients experienced haemorrhagic episodes. Bleeding was twice as frequent in patients over 59 years old as in those younger and no bleeding occurred in those less than 51 years of age. There was no correlation between frequency of bleeding and extent of thrombocytosis. Bleeding events occurred concurrently with use of anti-inflammatory agents in 32% of episodes. The gastrointestinal tract was the most frequent site. Documented thrombotic events occurred in three patients, two of whom had PV with haematocrits greater than 53%. This study suggests that the thrombocytosis of myeloproliferative processes may pose a less serious threat than originally thought and that aggressive lowering of the platelet count may not be indicated in all cases.
进行了一项回顾性研究,以检查与慢性骨髓增殖性疾病相关的未控制血小板增多症的自然病程。38例真性红细胞增多症(PV)、骨髓纤维化/髓样化生(MM)、慢性粒细胞白血病(CML)或原发性血小板增多症(ET)患者的血小板计数大于1000×10⁹/L,并进行了总共246患者年的密切随访。11例患者发生出血事件。59岁以上患者的出血频率是 younger患者的两倍,51岁以下患者未发生出血。出血频率与血小板增多程度之间无相关性。32%的出血事件与使用抗炎药同时发生。胃肠道是最常见的部位。3例患者发生有记录的血栓事件,其中2例为PV患者,血细胞比容大于53%。这项研究表明,骨髓增殖性疾病过程中的血小板增多症可能比最初认为的威胁较小,并且并非所有病例都需要积极降低血小板计数。