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An unusual precipitant of acute heart failure—ANCA-associated vasculitis in a patient with ischaemic cardiomyopathy: a case report

机译:患有缺血性心肌病的患者中急性心脏衰竭-ANCA相关血管炎的一种不寻常的沉淀剂:案例报告

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Background Antineutrophil cytoplasmic antibody (ANCA)-associated pulmonary renal vasculitis is an uncommon disease entity. Its presentation as acute heart failure for the first time in a patient with established coronary artery disease (CAD) is even rarer. We present here a case of such an association and an approach to managing this clinical situation. Case summary A 60-year-old male patient presented to the emergency room with recent-onset dyspnoea New York Heart Association Class IV. He was having hypertension, uncontrolled diabetes mellitus, chronic kidney disease (CKD), and CAD. He also underwent a percutaneous coronary intervention to left anterior descending in the past for acute coronary syndrome and had moderate left ventricular dysfunction. He was being managed as a case of acute decompensated heart failure (ADHF) and was mechanically ventilated. Suddenly his ventilator requirement increased and endotracheal aspirate contained blood. The chest radiograph showed bilateral hilar infiltrates. Simultaneously he also had recurrent episodes of ventricular tachycardia (VT) requiring direct current (DC) cardioversion. Blood investigations showed deranged renal function and severe hyperkalaemia, but no evidence of coagulopathy. High-resolution computed tomography chest showed features of diffuse alveolar haemorrhage. Further investigations revealed high titres of c-ANCA and raised inflammatory biomarkers. A diagnosis of ANCA-associated vasculitis presenting as acute on CKD with dyselectrolytaemia (hyperkalaemia) leading to VT was made. Apart from standard management for associated illness, he was treated with plasma exchange, steroids, and cyclophosphamide to which he responded and was later on discharged. Discussion Antineutrophil cytoplasmic antibody-related pulmonary renal vasculitis can lead to rapidly progressing renal failure and may present as ADHF in a patient with existent CAD. The associated VT storm in our patient can be attributed to hyperkalaemia secondary to acute renal failure. A multidisciplinary approach is required for the successful management of such a complex clinical scenario.
机译:背景技术抗替托硫醇细胞质抗体(ANCA) - 相加的肺肾血管炎是一种罕见的疾病实体。它的介绍是急性心力衰竭的第一次在患有冠状动脉疾病(CAD)的患者中甚至罕见。我们在这里展示了一种如此关联的案例和管理这种临床情况的方法。案例摘要一名60岁的男性患者提供给急诊室的近期呼救措施呼救室纽约心脏协会第四级。他具有高血压,不受控制的糖尿病,慢性肾病(CKD)和CAD。他还经历了一种经过经皮冠状动脉干预,留下过去的前期下降,以急性冠状动脉综合征,患有中度左心室功能障碍。他被视为急性失代偿性心力衰竭(ADHF)的情况,并机械通风。突然间,他的呼吸机要求增加,气管插管含有血液。胸部射线照片显示双侧肺炎犬浸润。同时他还具有反复发作的心室性心动过速(VT),需要直流(DC)心致。血液调查显示出紊乱的肾功能和严重的高钾血症,但没有凝血病的证据。高分辨率计算断层扫描胸显示弥漫性肺泡出血的特征。进一步调查显示出高滴度的C-ANCA和肿大的炎症生物标志物。 ANCA相关血管炎表现为急性上CKD与dyselectrolytaemia(高钾血症),导致VT的诊断为。除了相关疾病的标准管理外,他被血浆交换,类固醇和环磷酰胺治疗,他回应并后来被排放。讨论抗嗜酸性培养酚硫酸细胞质抗体相关的肺肾脉炎可导致较快进展肾功能衰竭,并且可以在存在CAD的患者中作为ADHF呈现。我们患者的相关vt风暴可归因于继发于急性肾功能衰竭的高钾血症。成功管理如此复杂的临床情景,需要多学科方法。

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