免疫性血小板减少症的治疗:从历史角度看背景。

IF 1.1 Q4 HEMATOLOGY Hematology Reports Pub Date : 2024-06-26 DOI:10.3390/hematolrep16030039
Daniel Martínez-Carballeira, Ángel Bernardo, Alberto Caro, Inmaculada Soto, Laura Gutiérrez
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引用次数: 0

摘要

免疫性血小板减少症(ITP)是一种自身免疫性疾病,其特点是血小板数量减少和出血风险增加。其发病机制复杂,影响免疫系统的多个组成部分,导致血小板外周破坏和骨髓生成不足。本文从历史角度回顾了 ITP 的治疗,讨论了一线和二线治疗以及难治性疾病的处理。
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Treatment of Immune Thrombocytopenia: Contextualization from a Historical Perspective.

Immune thrombocytopenia (ITP) is an autoimmune disease characterized by an isolated decrease in platelet count and an increased risk of bleeding. The pathogenesis is complex, affecting multiple components of the immune system and causing both peripheral destruction of platelets and inadequate production in the bone marrow. In this article, we review the treatment of ITP from a historical perspective, discussing first line and second line treatments, and management of refractory disease.

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来源期刊
Hematology Reports
Hematology Reports HEMATOLOGY-
CiteScore
0.90
自引率
0.00%
发文量
47
审稿时长
10 weeks
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