免疫介导的TTP继发于检查点抑制剂在IV期黑色素瘤患者中的应用。

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL BMJ Case Reports Pub Date : 2025-02-24 DOI:10.1136/bcr-2024-263705
Deevyashali Parekh, Michelle Liu, Yadu Nanda Subedi, Alina Basnet
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引用次数: 0

摘要

我们描述了一例中年男性IV期转移性黑色素瘤接受伊匹单抗/纳武单抗联合治疗。在接受第三周期治疗两周后,他以精神状态改变、急性肾损伤、发烧、贫血、实验室提示溶血和血小板计数为10出现在急诊室。他的计算血浆分数是6分。复查外周涂片证实有血吸虫细胞存在。他在住院期间接受了紧急血浆置换、大剂量类固醇、利妥昔单抗和卡普单抗治疗。患者对这种治疗反应良好,15天后最终出院,血小板计数大于200,血浆ADAMTS13水平较高(入院时未检测到)。越来越多的文献表明,继发于免疫治疗的血栓性血小板减少性紫癜(TTP)的可能性,因此需要对这些患者进行高度的怀疑,以便及时开始挽救生命的治疗。
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Immune-mediated TTP secondary to checkpoint inhibitor use in a patient with stage IV melanoma.

We describe the case of a middle-aged man with stage IV metastatic melanoma receiving ipilimumab/nivolumab combination therapy. Two weeks after receiving his third cycle of treatment, he presented to the emergency department with altered mental status, acute kidney injury, fever, anaemia with labs suggestive of haemolysis and a platelet count of 10. He had a calculated plasmic score of 6. A review of the peripheral smear confirmed the presence of schistocytes. He was treated with emergent plasma exchange, high-dose steroids, rituximab and caplacizumab throughout his hospitalisation. He had a good response to this treatment and was ultimately discharged to home 15 days later with a platelet count of greater than 200 and a high ADAMTS13 level in plasma (undetectable on admission).A growing body of literature suggests the possibility of thrombotic thrombocytopenic purpura (TTP) secondary to immunotherapy use, and thus a high index of suspicion is needed in these patients for timely, life-saving treatment initiation.

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来源期刊
BMJ Case Reports
BMJ Case Reports Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
1588
期刊介绍: BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.
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