Pembrolizumab-induced Triple M Overlap Syndrome, example of indiscriminate immune activation.

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL
Ben Schroeder, Emily Bosak, Nitish Nandu, Mary Mikhael
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引用次数: 0

Abstract

Triple M Overlap Syndrome is an ultra-rare and seldom-described immune-related adverse event (irAE) secondary to pembrolizumab therapy. This entity and its namesake are due to auto-immune phenomena involving myocardium, striated muscle and neuromuscular junction, yielding a syndrome of myocarditis, myositis and myasthenia gravis. Since it was first identified in 1975, only 100 cases of this syndrome are found in the literature. With the increasing use of immune checkpoint inhibitors (ICIs) for the treatment of various malignancies, however, more cases are likely to be diagnosed in the future. We present a patient who received her first cycle of pembrolizumab therapy 3 weeks prior to presentation with complaints of intense myalgias, diffuse muscle weakness and ptosis. Investigative workup revealed myocarditis, myositis and myasthenia gravis. Treatment with high-dose steroids plus plasma exchange drastically improved her symptoms. This case demonstrates the presenting symptoms, diagnostic findings, critical complications and management strategies of Triple M Overlap Syndrome.

pembrolizumab诱导的三重M重叠综合征,无差别免疫激活的例子。
三M重叠综合征是一种极罕见且很少被描述的免疫相关不良事件(irAE),继发于派姆单抗治疗。该实体及其同名是由于涉及心肌、横纹肌和神经肌肉连接处的自身免疫现象,产生心肌炎、肌炎和重症肌无力综合征。自1975年首次发现以来,文献中只发现了100例这种综合征。然而,随着免疫检查点抑制剂(ICIs)用于治疗各种恶性肿瘤的使用越来越多,未来可能会诊断出更多的病例。我们报告了一位患者,她在就诊前3周接受了第一个周期的派姆单抗治疗,主诉为强烈的肌痛,弥漫性肌肉无力和上睑下垂。检查结果为心肌炎、肌炎及重症肌无力。大剂量类固醇加上血浆置换治疗大大改善了她的症状。本病例展示了三M重叠综合征的表现、诊断结果、关键并发症和治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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