[Atrioventricular block in granulomatosis with polyangiitis (Wegener's granulomatosis). Case report and review of literature].

Luís Changuan R, René Asenjo G, Eduardo Sanhueza G, Raimundo Morris C, Mario Ortíz O
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Abstract

Granulomatosis with Polyangiitis (GPA), or Wegener's Granulomatosis, is an immunologically mediated systemic vasculitis of small and medium vessels, which commonly compromises the upper airway, lungs, and kidneys and is rarely associated with cardiac manifestations. Compromise of the cardiac conduction system is rare, and isolated cases of different degrees of atrioventricular block (AVB) have been described. We report a case of a 49-year-old male patient previously diagnosed with GPA 3 years ago, who presented to the emergency department with dyspnea, clinical signs of low output, bradycardia of 30/min, advanced second-degree AVB and complete left bundle branch block (LBBB) on the ECG. A literature review is presented, and we discuss the causes, evolution, and management of this GPA complication.

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[多血管炎肉芽肿病(韦格纳肉芽肿病)房室传导阻滞。病例报告和文献综述]。
多发性肉芽肿病(GPA)或韦格纳肉芽肿病是一种免疫介导的全身性中小血管炎,常见于上呼吸道、肺部和肾脏,很少伴有心脏表现。心脏传导系统受损的病例并不多见,但也有出现不同程度房室传导阻滞(AVB)的个别病例。我们报告了一例 49 岁男性患者的病例,该患者 3 年前曾被诊断为 GPA,因呼吸困难、低输出量临床表现、心动过缓 30 分/分钟、晚期二度房室传导阻滞和心电图显示完全性左束支传导阻滞(LBBB)而就诊于急诊科。本文回顾了相关文献,并讨论了这种 GPA 并发症的病因、演变和处理方法。
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