Godarzi Mohammad Taghi Hedayati, Rashid Mohamad, Abrotan Saeed, Fallah Marjan, Seifi Mehdi, Nikbakhsh Novin
Cardiology Department, Babol University of Medical Science, Gang Afroz Street, Babol, Iran.
Student Research Committee, Babol University of Medical Science, Babol, Iran.
BMC Cardiovasc Disord. 2025 Mar 27;25(1):225. doi: 10.1186/s12872-025-04681-0.
Myasthenia gravis (MG) is a rare autoimmune neuromuscular disorder in which autoantibodies impair neuromuscular junctions. MG can be associated with thymoma and with antibodies to the acetylcholine receptor (AChR), and is less commonly associated with antibodies to muscle-specific tyrosine kinase (MuSK). Treatment of AChR antibody-positive myasthenia gravis with the cholinesterase inhibitor, pyridostigmine, has known cardiac conduction side effects. Some reports indicate these cardiac effects, including bradyarrhythmias, occur more often with MuSK-ab positive MG. This report is of a 62-year-old man with recent onset muscle-specific tyrosine kinase (MuSK)-negative thymomatous myasthenia gravis presenting with bradycardia due to pyridostigmine-associated atrioventricular (AV) block.
A 62-year-old man presented with fluctuating muscle weakness, unilateral ptosis, mild dyspnea, and mild dysphagia. Laboratory testing was positive for acetylcholine receptor antibodies (AChR-ab), but negative for MuSK antibodies. Due to his symptoms, treatment with intravenous immunoglobulin (IVIg) and pyridostigmine was initiated. Mediastinal computed tomography scan (CT scan) revealed a thymoma. During thymectomy surgery, the patient experienced intraoperative asystole. After he was stabilized, episodes of high-degree atrioventricular (AV) block were seen on postoperative ambulatory rhythm monitoring. Therefore, a permanent pacemaker (PPM) was implanted before repeat thymectomy, which was performed without complications Histopathological examination of the thymic tissue demonstrated a type B1 thymoma.
This report has highlighted the importance of accurate diagnosis of MG and its autoimmune subtypes, and if treatment is required with pyridostigmine, the importance of follow-up and electrocardiographic monitoring to ensure the rapid diagnosis and management of cardiac conduction abnormalities, even if they are MuSK antibody-negative.
重症肌无力(MG)是一种罕见的自身免疫性神经肌肉疾病,其中自身抗体损害神经肌肉接头。MG可与胸腺瘤以及抗乙酰胆碱受体(AChR)抗体相关,较少与抗肌肉特异性酪氨酸激酶(MuSK)抗体相关。用胆碱酯酶抑制剂吡啶斯的明治疗AChR抗体阳性的重症肌无力有已知的心脏传导副作用。一些报告表明,这些心脏效应,包括缓慢性心律失常,在MuSK抗体阳性的MG中更常见。本报告是关于一名62岁男性,近期发病的肌肉特异性酪氨酸激酶(MuSK)阴性胸腺瘤型重症肌无力,因吡啶斯的明相关的房室(AV)阻滞而出现心动过缓。
一名62岁男性出现波动性肌无力、单侧上睑下垂、轻度呼吸困难和轻度吞咽困难。实验室检查乙酰胆碱受体抗体(AChR-ab)呈阳性,但MuSK抗体呈阴性。由于他的症状,开始用静脉注射免疫球蛋白(IVIg)和吡啶斯的明治疗。纵隔计算机断层扫描(CT扫描)显示有胸腺瘤。在胸腺切除手术中,患者术中出现心搏停止。在他病情稳定后,术后动态心律监测发现有高度房室(AV)阻滞发作。因此,在重复胸腺切除术前植入了永久性起搏器(PPM),该手术无并发症。胸腺组织的组织病理学检查显示为B1型胸腺瘤。
本报告强调了准确诊断MG及其自身免疫亚型的重要性,以及如果需要用吡啶斯的明治疗,随访和心电图监测对于确保快速诊断和处理心脏传导异常的重要性,即使是MuSK抗体阴性的情况。