Sun Keyue, Guo Fan, Xu Xiqi, Liu Yongtai
Department of Cardiology, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences, Beijing, China.
Front Cardiovasc Med. 2025 May 12;12:1573539. doi: 10.3389/fcvm.2025.1573539. eCollection 2025.
Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) typically manifests in the first weeks of life. We report a 28-year-old woman with atrial fibrillation and pulmonary hypertension which were later found to be associated with ALCAPA syndrome. Despite a history free of traditional cardiovascular risk factors, her symptoms included exercise intolerance, palpitations, and an ischemic stroke. Echocardiography and further examination revealed pulmonary artery origin of the left coronary artery and extensive collateral formation between the left and right coronary arteries, contributing to her symptoms.
左冠状动脉起源于肺动脉(ALCAPA)通常在出生后的头几周出现症状。我们报告了一名28岁女性,她患有心房颤动和肺动脉高压,后来发现与ALCAPA综合征有关。尽管她没有传统的心血管危险因素病史,但她的症状包括运动不耐受、心悸和缺血性中风。超声心动图和进一步检查显示左冠状动脉起源于肺动脉,左右冠状动脉之间有广泛的侧支形成,这导致了她的症状。