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极度血小板增多症:病因有哪些?

Extreme thrombocytosis: what are the etiologies?

作者信息

Wiwanitkit Viroj

机构信息

Department of Laboratory Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

出版信息

Clin Appl Thromb Hemost. 2006 Jan;12(1):85-7. doi: 10.1177/107602960601200113.

Abstract

Increase platelet count or thrombocytosis, defined as a platelet count greater than or equal to 350 x 10(9)/L, is a common hematologic aberration seen in complete blood cell count. Several etiologies are documented for thrombocytosis. Extreme thrombocytosis, defined as a platelet count greater than or equal to 1,000 x 10(9)/L, is rarely seen in general practice. There are limited data on the etiology of this abnormality. Here, a retrospective investigation for the etiology of severe thrombocytosis was performed. Of the 3 included reports, 535 cases with extreme thrombocytosis were investigated for their etiologies. The 2 defined etiologies are secondary thrombocytosis (66.6%) and clonal thrombocytosis. Of those cases with clonal thrombocytosis, 93.8% had myeloproliferative disorders, and 6.2% had essential thrombocytosis. Concerning bleeding and vaso-occlusive complications, all cases had these complications. In this study, 7.9% of the cases with secondary thrombocytosis experienced bleeding and vaso-occlusive complications, while 17.1% of the cases with clonal thrombocytosis did.

摘要

血小板计数增加或血小板增多症,定义为血小板计数大于或等于350×10⁹/L,是全血细胞计数中常见的血液学异常。血小板增多症有多种病因记录在案。极端血小板增多症,定义为血小板计数大于或等于1000×10⁹/L,在一般临床实践中很少见。关于这种异常的病因数据有限。在此,对严重血小板增多症的病因进行了一项回顾性调查。在纳入的3份报告中,对535例极端血小板增多症病例的病因进行了调查。确定的两种病因是继发性血小板增多症(66.6%)和克隆性血小板增多症。在那些克隆性血小板增多症病例中,93.8%患有骨髓增殖性疾病,6.2%患有原发性血小板增多症。关于出血和血管闭塞性并发症,所有病例均有这些并发症。在本研究中,继发性血小板增多症病例中有7.9%出现出血和血管闭塞性并发症,而克隆性血小板增多症病例中有17.1%出现这些并发症。

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