首页> 外文期刊>Transfusion and apheresis science: official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis >A case for consideration by apheresis practitioners: Melanoma and PD-1 inhibitor treatment in a patient with multiple relapses of immune thrombotic thrombocytopenic purpura
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A case for consideration by apheresis practitioners: Melanoma and PD-1 inhibitor treatment in a patient with multiple relapses of immune thrombotic thrombocytopenic purpura

机译:采用筛查员的案例审议:黑色素瘤和PD-1抑制剂治疗在免疫血栓形成血小板诱导紫癜多重复发的患者中

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摘要

Thrombotic Thrombocytopenic Purpura (TTP) is a rare life-threatening disease caused by ADAMTS-13 deficiency. Up to forty percent of patients with TTP relapse, and most relapse within eight years of their first presentation. This case report describes a patient with an aggressive course of TIP who subsequently developed metastatic melanoma while receiving prophylactic rituximab. Limited data exists regarding the potential for malignancy in patients receiving Rituximab for benign conditions. This is the first published case of melanoma in a TIP patient treated with rituximab. Melanoma treatment with PD-1 inhibitors is also associated with worsening of pre-existing autoimmune conditions. In this case, a splenectomy resulted in a durable remission despite treatment with PD-1 inhibitor.
机译:血栓形成血小板减少紫癜(TTP)是由Adamts-13缺乏引起的罕见危及生命的疾病。 高达40%的TTP复发患者,并且在其第一次演示中八年内复发。 本病例报告描述了一种患者,其具有尖端的侵略性课程,其随后在接受预防性戒指的同时出现转移性黑色素瘤。 有限的数据存在关于接受良性条件的Rituximab患者的恶性肿瘤潜力。 这是用Rituximab处理的尖端患者中第一个发表的黑色素瘤的情况。 用PD-1抑制剂的黑色素瘤治疗也与预先存在的自身免疫条件恶化有关。 在这种情况下,尽管用PD-1抑制剂治疗,脾切除术导致耐用的缓解。

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