Thrombocytosis: diagnostic evaluation, thrombotic risk stratification, and risk-based management strategies.

Thrombosis Pub Date : 2011-01-01 Epub Date: 2011-06-08 DOI:10.1155/2011/536062
Jonathan S Bleeker, William J Hogan
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引用次数: 105

Abstract

Thrombocytosis is a commonly encountered clinical scenario, with a large proportion of cases discovered incidentally. The differential diagnosis for thrombocytosis is broad and the diagnostic process can be challenging. Thrombocytosis can be spurious, attributed to a reactive process or due to clonal disorder. This distinction is important as it carries implications for evaluation, prognosis, and treatment. Clonal thrombocytosis associated with the myeloproliferative neoplasms, especially essential thrombocythemia and polycythemia vera, carries a unique prognostic profile, with a markedly increased risk of thrombosis. This risk is the driving factor behind treatment strategies in these disorders. Clinical trials utilizing targeted therapies in thrombocytosis are ongoing with new therapeutic targets waiting to be explored. This paper will outline the mechanisms underlying thrombocytosis, the diagnostic evaluation of thrombocytosis, complications of thrombocytosis with a special focus on thrombotic risk as well as treatment options for clonal processes leading to thrombocytosis, including essential thrombocythemia and polycythemia vera.

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血小板增多症:诊断评估,血栓风险分层,以及基于风险的管理策略。
血小板增多症是一种常见的临床症状,很大一部分病例是偶然发现的。血小板增多症的鉴别诊断是广泛的,诊断过程可能是具有挑战性的。血小板增多症可以是假的,归因于反应过程或由于克隆紊乱。这种区别很重要,因为它对评估、预后和治疗都有影响。与骨髓增生性肿瘤相关的克隆性血小板增多症,特别是原发性血小板增多症和真性红细胞增多症,具有独特的预后特征,血栓形成的风险显著增加。这种风险是这些疾病治疗策略背后的驱动因素。临床试验利用靶向治疗在血小板增多正在进行新的治疗靶点等待探索。本文将概述血小板增多的机制,血小板增多的诊断评估,血小板增多的并发症,特别关注血栓形成风险,以及导致血小板增多的克隆过程的治疗选择,包括原发性血小板增多症和真性红细胞增多症。
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