08 June 2026
: Case report
[In Press] Chest Pain Due to Anomalous Origin of the Left Circumflex Artery From the Opposite Sinus of Valsalva in a 70-Year-Old Woman
Challenging differential diagnosis, Rare disease, Congenital defects / diseases
Tian Luo1EF, Kang Luo1B, JunBing Lin1D, Qiang Huang1ADOI: 10.12659/AJCR.952577
Am J Case Rep In Press; DOI: 10.12659/AJCR.952577
Available online: 2026-06-08, In Press, Corrected Proof
Publication in the "In-Press" formula aims at speeding up the public availability of the pending manuscript while waiting for the final publication. The assigned DOI number is active and citable. The availability of the article in the Medline, PubMed and PMC databases as well as Web of Science will be obtained after the final publication according to the journal schedule
Abstract
BACKGROUND
An anomalous origin of a coronary artery from the opposite sinus of Valsalva (ACAOS) is a rare congenital coronary abnormality that is usually asymptomatic throughout life. However, an anomalous coronary artery arising from an atypical aortic location can lead to myocardial ischemia, exertional symptoms, or even sudden cardiac death. Therefore, early recognition and risk stratification are essential. Clinical management of ACAOS should be highly individualized and guided by detailed anatomical features, clinical symptoms, and evidence of ischemia. This report describes an older woman who presented with new-onset chest pain as the first clinical manifestation of previously undiagnosed ACAOS.
CASE REPORT
A 70-year-old woman presented with 5 days of progressive chest tightness and 20 days of recurrent dizziness associated with poorly controlled hypertension. Initial conventional medical therapy provided inadequate symptom relief. Subsequent coronary angiography revealed an anomalous left circumflex artery originating independently from the right sinus of Valsalva, with 3 separate coronary ostia and concurrent clinically significant atherosclerotic stenosis. She underwent uncomplicated percutaneous coronary intervention of the right coronary artery, achieving successful revascularization and complete resolution of her presenting symptoms.
CONCLUSIONS
This report describes a rare case of ACAOS presenting with de novo chest pain in an older woman, highlighting the critical importance of accurate anatomical characterization and tailored, individualized management for optimal clinical outcomes.
Keywords: Cardiology; Congenital Abnormalities; Coronary Artery Disease; Coronary Vessel Anomalies; Review; Atherosclerosis; Coronary Angiography; Tomography, X-Ray Computed; Case Reports
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