Song Yun-Seok, Seol Sang-Hoon, Park Jino, Kim Dong-Kie, Song Yeo-Jeong, Kim Seunghwan, Kim Ki-Hun, Kim Doo-Il, Park Chan-Seon, Kim Yeon-Mi
Department of Internal Medicine, Haeundae Paik Hospital, Inje University College of Medicine, Busan, Korea.
Department of Internal Medicine, Haeundae Paik Hospital, Inje University College of Medicine, Busan, Korea. Email:
Cardiovasc J Afr. 2020 Mar/Apr;31(4):e1-e4. doi: 10.5830/CVJA-2019-065. Epub 2020 Jan 29.
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare form of systemic vasculitis in which cardiac involvement is relatively common and accounts for half of EGPA-related deaths. Cardiac involvement is more frequent in patients with an absence of anti-neutrophil cytoplasmic antibody and those with higher eosinophil counts. Clinical manifestations are various, including myocarditis, pericarditis, pericardial effusion, heart failure, arrhythmias, valvular insufficiencies and intra-cardiac thrombus formation. The pathology of cardiac involvement in EGPA is usually endomyocardial and pericardial eosinophilic infiltration. Considering the potentially adverse outcomes associated with cardiac involvement in EGPA, early detection is important. We experienced a rare case of EGPA with cardiac involvement presenting with non-infectious vegetations.
嗜酸性肉芽肿性多血管炎(EGPA)是一种罕见的系统性血管炎,其中心脏受累较为常见,占EGPA相关死亡病例的一半。在无抗中性粒细胞胞浆抗体的患者和嗜酸性粒细胞计数较高的患者中,心脏受累更为频繁。临床表现多样,包括心肌炎、心包炎、心包积液、心力衰竭、心律失常、瓣膜关闭不全和心内血栓形成。EGPA心脏受累的病理通常是心内膜和心包嗜酸性粒细胞浸润。鉴于EGPA心脏受累可能带来不良后果,早期检测很重要。我们遇到了一例罕见的EGPA心脏受累病例,表现为非感染性赘生物。