Chronic active myocarditis presenting as an isolated atrioventricular block: a case report.

IF 0.8 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
European Heart Journal: Case Reports Pub Date : 2025-09-16 eCollection Date: 2025-10-01 DOI:10.1093/ehjcr/ytaf454
Kazuhiro Asano, Masahiko Noguchi, Kisaki Amemiya, Yoshihiko Ikeda, Kotaro Obunai
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引用次数: 0

Abstract

Background: Although atrioventricular (AV) block is frequently observed in acute myocarditis, its occurrence as an isolated finding in chronic myocarditis is rare. Chronic active myocarditis represents an uncommon subset of myocarditis with a potentially poor prognosis. Herein, we report a rare case of chronic active myocarditis presenting solely as an isolated AV block.

Case summary: A 51-year-old female with ulcerative colitis and bipolar disorder presented with complete AV block. Echocardiography revealed preserved cardiac function, whereas laboratory findings revealed persistently elevated troponin I levels. Despite extensive investigations, no definitive cause of conduction disturbance was identified, leading to pacemaker implantation. Ten months later, 18-fluoro-deoxyglucose positron emission tomography/computed tomography (18F-FDG-PET/CT) revealed diffuse cardiac uptake; endomyocardial biopsy demonstrated inflammatory infiltrates adjacent to the cardiomyocyte necrosis and fibrosis. These findings were consistent with those of chronic active myocarditis. As the patient's symptoms were mild and cardiac function was preserved, a conservative approach was adopted. Over the next 2 years, the patient's symptoms improved, cardiac function was preserved, and the FDG-PET/CT findings markedly diminished. However, high-uptake areas remained on FDG-PET/CT and re-elevation of troponin I was observed, indicating the persistence of subclinical inflammation within the myocardium.

Discussion: AV block may be a clinical sequela of chronic active myocarditis and should not be considered idiopathic, even in the absence of inflammatory symptoms or systolic dysfunction. Such cases may carry a risk of poor long-term outcomes due to ongoing inflammation. Endomyocardial biopsy should therefore be considered to establish an accurate diagnosis, and long-term follow-up is essential.

慢性活动性心肌炎表现为孤立的房室传导阻滞1例。
背景:虽然房室传导阻滞在急性心肌炎中很常见,但在慢性心肌炎中作为孤立的发现是罕见的。慢性活动性心肌炎是一种少见的心肌炎,具有潜在的不良预后。在此,我们报告一例罕见的慢性活动性心肌炎,仅表现为孤立的房室传导阻滞。病例总结:51岁女性溃疡性结肠炎和双相情感障碍表现为完全性房室传导阻滞。超声心动图显示保留心功能,而实验室结果显示肌钙蛋白I水平持续升高。尽管进行了广泛的调查,但没有确定导致起搏器植入的传导障碍的确切原因。10个月后,18-氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(18F-FDG-PET/CT)显示弥漫性心脏摄取;心内膜活检显示炎症浸润邻近心肌细胞坏死和纤维化。这些结果与慢性活动性心肌炎一致。由于患者症状较轻,心功能保留,故采取保守治疗。在接下来的2年里,患者的症状得到改善,心功能得到保留,FDG-PET/CT表现明显下降。然而,FDG-PET/CT显示,高摄取区域仍然存在,肌钙蛋白I再次升高,表明心肌内亚临床炎症持续存在。讨论:房室传导阻滞可能是慢性活动性心肌炎的临床后遗症,即使没有炎症症状或收缩功能障碍,也不应被认为是特发性的。由于持续的炎症,这些病例可能有长期预后不良的风险。因此,应考虑心内膜活检以建立准确的诊断,长期随访是必要的。
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
European Heart Journal: Case Reports
European Heart Journal: Case Reports Medicine-Cardiology and Cardiovascular Medicine
CiteScore
1.30
自引率
10.00%
发文量
451
审稿时长
14 weeks
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