一例罕见的wegner肉芽肿病表现为完全性心脏传导阻滞

Q4 Medicine
Rahul Singla, N. Waghmare, Aniruddha M. Kaushik, Anil Kumar, N. Bansal
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引用次数: 0

摘要

心脏受累见于6%至25%的韦格纳肉芽肿病,但很少涉及传导系统,表现为完全性心脏传导阻滞。早些时候,大多数病例报告都是系统性变异,而不是局限性变异。我们报告了一例局限性韦格纳肉芽肿病患者的完全性心脏传导阻滞(3度),该患者接受了永久性起搏器植入治疗。完全性房室传导阻滞是韦格纳斯肉芽肿病心脏受累的一种罕见但可治疗的表现,通常与早期活动性全身性疾病有关。所有被诊断为韦格纳肉芽肿病的患者都应通过基线心电图和经胸超声心动图进行筛查,以记录心脏受累情况,并提醒临床医生注意那些有进一步心脏并发症风险的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Rare Presentation of Wegners Granulomatosis as Complete Heart Block
Cardiac involvement is seen in 6 to 25% Wegener’s granulomatosis, but very rarely it can involve the conduction system and manifest as complete heart block. Earlier most of the case reports were with systemic variant rather than a limited variant. We report a case of complete Heart Block (3rd degree) in a case of limited Wegner granulomatosis which was treated with Permanent Pacemaker Implantation. Complete AV block is a rare but treatable manifestation of cardiac involvement of wegners granulomatosis usually associated with early active systemic disease. All patients diagnosed with Wegener’s granulomatosis should be screened with a baseline electrocardiogram and a transthoracic echocardiogram to document cardiac involvement and alert clinicians to those at risk of further cardiac complications.
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来源期刊
Journal of Cardiovascular Disease Research
Journal of Cardiovascular Disease Research Medicine-Cardiology and Cardiovascular Medicine
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