ISSN 2097-5724 CN 61-1535/R 主管·主办:陕西省疾病预防控制中心
疾病预防与控制 Disease Prevention and Control 医学学术期刊 双月刊
2025-04-025 临床药物应用 2025, (04)

一例免疫检查点抑制剂相关的重症肌无力及艾加莫德治疗

延安大学 2.榆林市第一医院

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摘要

目的 探讨免疫检查点抑制剂相关的重症肌无力(ICIs-MG)的临床特征及艾加莫德的治疗效果,为临床实践提供参考。方法 对榆林市第一医院收治的一例免疫检查点抑制剂相关的重症肌无力患者的临床资料进行回顾性分析。结果 患者老年男性,重症肌无力症状典型,既往有免疫检查点抑制剂使用史,诊断为免疫检查点抑制剂相关的重症肌无力。入院后停用免疫检查点抑制剂,联合甲泼尼龙琥珀酸钠及丙种球蛋白治疗,但气短症状无明显缓解;予以溴吡斯的明后眼睑下垂有好转;与患者及家属沟通后予以艾加莫德治疗,激素用量根据相关治疗指南及患者情况逐渐减量,治疗后患者气短等症状逐渐好转,相关指标明显下降。出院后继续上述治疗方案,半月后复查,患者再未发生肌无力相关症状,复查相关指标基本正常。结论 此类病例临床少见,病情严重,进展迅速,并且死亡率高,需要早期诊断与及时治疗。将此例病例予以报道,为类似病例的临床管理提供参考。

Abstract

Objective To investigate the clinical characteristics of immune checkpoint inhibitor associated myasthenia gravis (ICIs-MG) and the therapeutic efficacy of efgartigimod, providing reference for clinical practice. Methods A retrospective analysis was conducted on the clinical data of a patient with immune checkpoint inhibitor associated myasthenia gravis treated at Yulin First Hospital. Results The patient was an elderly male with a history of immune checkpoint inhibitor use, presented with typical symptoms of myasthenia gravis and was diagnosed with immune checkpoint inhibitor associated myasthenia gravis. After admission, immune checkpoint inhibitors were discontinued, and treatment with methylprednisolone succinate and intravenous immunoglobulin was initiated. However, the symptoms of dyspnea did not significantly improve. Improvement in ptosis was observed after the administration of pyridostigmine bromide. Following discussion with the patient and family, efgartigimod was introduced, with corticosteroid dosage tapered gradually according to guidelines and the patient’ s condition. After treatment,the patient’ s symptoms of dyspnea and other related symptoms gradually improved, and relevant laboratory indicators significantly decreased. The patient continued the same treatment regimen after discharge. A follow-up examination two weeks later revealed no recurrence of myasthenia gravis symptoms, and the rechecked indicators were essentially normal. Conclusion Immune checkpoint inhibitor associated myasthenia gravis is a rare clinical condition characterized by severe and rapidly progressive disease, with a high mortality rate. Early diagnosis and prompt treatment are crucial.This case is reported here to provide a reference for the clinical management of similar cases.

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[1]肖梦妮,朱江,刘瑞,等.一例免疫检查点抑制剂相关的重症肌无力及艾加莫德治疗[J],2025,01(04):.