Le Van Lam MD, Truong Minh Thuong MD, Tran Quyet Thang MD, Vu Thi Thuy Huong MD, Tran Minh Vu MD, Hoang Phan Thu Ha BSc, Duong Dinh Tuan Linh BSc, Phung Xuan Thinh BSc
{"title":"Rare congenital coronary artery anomalies diagnosed by coronary CT angiography: A 4-case series","authors":"Le Van Lam MD, Truong Minh Thuong MD, Tran Quyet Thang MD, Vu Thi Thuy Huong MD, Tran Minh Vu MD, Hoang Phan Thu Ha BSc, Duong Dinh Tuan Linh BSc, Phung Xuan Thinh BSc","doi":"10.1016/j.radcr.2025.09.029","DOIUrl":null,"url":null,"abstract":"<div><div>Congenital coronary artery anomalies (CCAAs) are uncommon but may cause myocardial ischemia, arrhythmias, or sudden cardiac death. Coronary computed tomography angiography (CCTA) provides precise, noninvasive assessment of these variants. We report 4 rare CCAA cases detected by CCTA: (1) coronary cameral fistula from the left coronary artery (LCA) to the left ventricle with associated myocardial bridging; (2) interarterial course of the right coronary artery (RCA) between the aorta and pulmonary artery; (3) congenital absence of the RCA with a dominant left system; and (4) dual RCAs. Three patients presented with exertional chest pain, one was found incidentally. All were managed conservatively based on absence of hemodynamic compromise and low ischemic risk; symptoms resolved or improved on follow-up (3-12 months). This series illustrates the spectrum of rare CCAAs and emphasizes CCTA’s role in differentiating malignant from benign variants, guiding management, and avoiding unnecessary interventions.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"21 1","pages":"Pages 59-64"},"PeriodicalIF":0.0000,"publicationDate":"2025-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Radiology Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1930043325008659","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Congenital coronary artery anomalies (CCAAs) are uncommon but may cause myocardial ischemia, arrhythmias, or sudden cardiac death. Coronary computed tomography angiography (CCTA) provides precise, noninvasive assessment of these variants. We report 4 rare CCAA cases detected by CCTA: (1) coronary cameral fistula from the left coronary artery (LCA) to the left ventricle with associated myocardial bridging; (2) interarterial course of the right coronary artery (RCA) between the aorta and pulmonary artery; (3) congenital absence of the RCA with a dominant left system; and (4) dual RCAs. Three patients presented with exertional chest pain, one was found incidentally. All were managed conservatively based on absence of hemodynamic compromise and low ischemic risk; symptoms resolved or improved on follow-up (3-12 months). This series illustrates the spectrum of rare CCAAs and emphasizes CCTA’s role in differentiating malignant from benign variants, guiding management, and avoiding unnecessary interventions.
期刊介绍:
The content of this journal is exclusively case reports that feature diagnostic imaging. Categories in which case reports can be placed include the musculoskeletal system, spine, central nervous system, head and neck, cardiovascular, chest, gastrointestinal, genitourinary, multisystem, pediatric, emergency, women''s imaging, oncologic, normal variants, medical devices, foreign bodies, interventional radiology, nuclear medicine, molecular imaging, ultrasonography, imaging artifacts, forensic, anthropological, and medical-legal. Articles must be well-documented and include a review of the appropriate literature.