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首页> 外文期刊>British Journal of Haematology >Salvage therapy of autoimmune thrombocytopenic purpura revealing non-Hodgkin lymphoma by the thrombopoietin receptor agonist romiplostim.
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Salvage therapy of autoimmune thrombocytopenic purpura revealing non-Hodgkin lymphoma by the thrombopoietin receptor agonist romiplostim.

机译:血小板生成素受体激动剂罗米洛司汀对自身免疫性血小板减少性紫癜的挽救疗法揭示了非霍奇金淋巴瘤。

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摘要

Immune Thrombocytopenic Purpura (ITP) is an autoimmune disease that mainly results from a rapid splenic and hepatic clearance of autoantibody-loaded platelets from the circulation (Koehrer et al, 2010). Secondary causes of ITP must be excluded at diagnosis, including autoimmune conditions, chronic infection (e.g. Hepatitis C virus, human immunodeficiency virus) and lymphoproliferative disorders (LPD), particularly B-cell chronic lymphocytic leukaemia (B-CLL) (Cines et al, 2009). Treatment options for idiopathic ITP are. well defined, including steroids, intravenous immunoglobulins (IVIG) in acute ITP, and the anti-CD20 monoclonal antibody rituximab, splenectomy and immune suppressive drugs in chronic ITP (George, 2010).
机译:免疫性血小板减少性紫癜(ITP)是一种自身免疫性疾病,主要是由于循环中自身抗体加载的血小板从脾脏和肝脏的快速清除所致(Koehrer等,2010)。诊断时必须排除ITP的继发原因,包括自身免疫性疾病,慢性感染(例如丙型肝炎病毒,人类免疫缺陷病毒)和淋巴细胞增生性疾病(LPD),尤其是B细胞慢性淋巴细胞性白血病(B-CLL)(Cines等, 2009)。特发性ITP的治疗选择是。定义明确的药物,包括急性ITP中的类固醇,静脉免疫球蛋白(IVIG),以及慢性ITP中的抗CD20单克隆抗体利妥昔单抗,脾切除术和免疫抑制药物(George,2010)。

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