Khan Shahkar, Rizvi Taqi A, Velaga Saran Teja, Ling Joanne C, Makhoul Wahbah Gennifer, Asogwa Nnedindu, Ahmed Mustafa, Lafferty James C
Internal Medicine, Northwell Health/Staten Island University Hospital, Staten Island, USA.
Cardiology, Northwell Health/Staten Island University Hospital, Staten Island, USA.
Cureus. 2023 Feb 8;15(2):e34774. doi: 10.7759/cureus.34774. eCollection 2023 Feb.
Granulomatosis with polyangiitis (GPA) is an autoimmune disease that affects small and medium-sized vessels. It is classically known to present with renal and respiratory tract symptoms. However, the disease can manifest in other organ systems, especially cardiovascular involvement. Though there are multiple reports of cardiac involvement in GPA, it is not commonly evaluated and is often overlooked in patients with GPA. Heart disease in GPA has a wide range of presentations ranging from subacute and silent to severe abnormalities, which can prove fatal if not identified and treated appropriately. Identifying cardiac involvement early in patients with no apparent signs can help with prevention strategies and follow-up to avoid significant complications. Pericarditis is the most common pathology noted in GPA, followed by cardiomyopathy, coronary artery disease, valvular disease, and conduction abnormality. In our report, we present a case of GPA in a young male with asymptomatic conduction abnormality of the heart. Although it was silent at the presentation, identifying the initial electrocardiogram (ECG) changes prompted us to admit him to the telemetry floor. Continuous telemetry monitoring helped us identify the progression of the conduction abnormality, which otherwise could have been missed. This led us to correlate to his symptoms which he later developed during his admission course. His symptoms subsided after prompt treatment. If not identified early, these cardiac abnormalities can delay management, leading to increased disease burden and morbidity. Hence, essential cardiac work with at least ECG and continuous telemetry monitoring is recommended.
肉芽肿性多血管炎(GPA)是一种影响中小血管的自身免疫性疾病。其典型表现为肾脏和呼吸道症状。然而,该疾病可累及其他器官系统,尤其是心血管系统。尽管有多项关于GPA累及心脏的报道,但通常对其评估不足,在GPA患者中常被忽视。GPA相关的心脏病表现多样,从亚急性和无症状到严重异常,若未得到及时识别和恰当治疗,可能会致命。在无明显体征的患者中早期识别心脏受累情况,有助于制定预防策略和进行随访,以避免严重并发症。心包炎是GPA中最常见的病理表现,其次是心肌病、冠状动脉疾病、瓣膜病和传导异常。在我们的报告中,我们呈现了一例年轻男性GPA患者,其存在无症状性心脏传导异常。尽管在初诊时无症状,但识别出最初的心电图(ECG)变化促使我们将他收治到遥测病房。持续的遥测监测帮助我们识别出传导异常的进展情况,否则可能会被漏诊。这使我们将其与他在住院期间后来出现的症状联系起来。经过及时治疗,他的症状得到缓解。如果早期未被识别,这些心脏异常可能会延误治疗,导致疾病负担和发病率增加。因此,建议至少进行心电图和持续遥测监测等基本的心脏检查。