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Thrombocytosis: Diagnostic Evaluation, Thrombotic Risk Stratification, and Risk-Based Management Strategies

机译:血小板增多症:诊断评估,血栓形成风险分层和基于风险的管理策略

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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.
机译:血小板增多症是一种常见的临床情况,偶然发现了大量病例。血小板增多症的鉴别诊断广泛,诊断过程可能具有挑战性。血小板增多症可能是虚假的,归因于反应性过程或克隆性疾病。这种区别很重要,因为它会对评估,预后和治疗产生影响。与骨髓增生性肿瘤相关的克隆性血小板增多症,尤其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,血栓形成的风险显着增加。在这些疾病中,这种风险是治疗策略背后的驱动因素。正在进行针对血小板增多症的靶向治疗的临床试验,目前正在探索新的治疗靶标。本文将概述血栓形成的潜在机制,血栓形成的诊断评估,血栓形成的并发症,并特别着重于血栓形成的风险以及导致血栓形成的克隆过程的治疗选择,包括必需的血小板增多症和真性红细胞增多症。

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