硫唑嘌呤超敏综合征导致的可逆性左心室功能障碍病例报告

Daniel Lüscher, Micha T Maeder, Eva Scheler
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引用次数: 0

摘要

在使用硫唑嘌呤(AZA)进行免疫抑制治疗期间,过敏反应是一种罕见的副作用。已有一些心脏受累病例的报道,但因果关系很难证明。 我们介绍了一名 68 岁男性的病例,他曾两次出现可逆性左心室(LV)功能障碍。在开始使用 AZA 治疗一个月后,他出现了非特异性症状,包括轻微胸痛。在心脏生物标志物和炎症标志物升高的情况下,超声心动图显示左心室收缩功能减退。心脏磁共振成像(CMR)显示双心室功能障碍,但未发现心肌水肿或晚期钆增强。停用 AZA 后,左心室功能完全恢复。在重新开始 AZA 治疗后的早期,临床病程和超声心动图检查结果非常相似。最终停用 AZA 后,左心室收缩功能再次恢复,并在长期随访中保持稳定。 AZA 导致心脏受累的超敏反应非常罕见。与 AZA 相关的心脏功能障碍的确切机制仍未完全明了,因果关系往往难以证明。然而,由于再次接触该药物(回想起来并不恰当),我们的患者明显受到了影响。了解 AZA 治疗的这种可能危及生命的副作用非常重要。如果有任何超敏反应的证据,必须立即停用 AZA。
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A case report of reversible left ventricular dysfunction due to azathioprine hypersensitivity syndrome
Hypersensitivity reaction is a rare side effect during immunosuppressive treatment with azathioprine (AZA). Some cases of cardiac involvement have already been reported but causality is notoriously difficult to prove. We present the case of a 68-year-old man with two episodes of reversible left ventricular (LV) dysfunction. One month after treatment initiation with AZA, he developed non-specific symptoms, including mild chest pain. In the context of elevated cardiac biomarkers and markers of inflammation, echocardiography showed depressed systolic LV function. Biventricular dysfunction was shown on cardiac magnetic resonance imaging (CMR), but neither myocardial oedema nor late gadolinium enhancement was documented. There was full recovery of LV function after AZA discontinuation. Very similar clinical course and echocardiography findings were observed early after restarting AZA treatment. After definitive cessation of AZA, systolic LV function recovered again and remained stable throughout long-term follow-up. Hypersensitivity reaction with cardiac involvement due to AZA is rare. The exact mechanisms underlying AZA-related cardiac dysfunction are still not completely understood, and causality is often difficult to prove. However, because of re-exposure to the drug, which, considered retrospectively, was inappropriate, the effect was clearly apparent in our patient. Knowledge of this potentially life-threatening side effect of AZA treatment is important. AZA must be discontinued promptly if there is any evidence of hypersensitivity reaction.
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