脾切除术后难治性ITP伴致死性血栓栓塞的极端血小板增多

IF 1.9 Q3 PATHOLOGY Clinical Pathology Pub Date : 2022-01-01 DOI:10.1177/2632010X221083218
R. Nedumannil, E. Leitinger, S. Juneja
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引用次数: 0

摘要

血小板生成素(TPO)受体激动剂预示着治疗难治性免疫性血小板减少症(ITP)的范式转变。反应性血小板增多症已被描述为此类疗法的次要作用。然而,在这种情况下,出现形态类似骨髓增生性肿瘤(MPN)的极端血小板增多现象,然后出现致命的血栓栓塞是不常见的。在诊断难治性ITP以及在这种情况下给药TPO受体激动剂时需要谨慎。
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Extreme Thrombocytosis in Refractory ITP Post-Splenectomy With Associated Fatal Thromboembolism
Thrombopoietin (TPO)-receptor agonists have heralded a paradigm shift in the treatment of refractory immune thrombocytopenia (ITP). Reactive thrombocytosis has been described as a secondary effect of such therapies. However, the phenomenon of extreme thrombocytosis with morphology mimicking a myeloproliferative neoplasm (MPN) followed by fatal thromboembolism is unusual in this setting. Caution is required in the diagnosis of refractory ITP as well as TPO-receptor agonist dosing in such cases.
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来源期刊
Clinical Pathology
Clinical Pathology PATHOLOGY-
CiteScore
2.20
自引率
7.70%
发文量
66
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