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Anomalous aortic origin of right coronary artery from left coronary cusp: a management conundrum: a case report

BACKGROUND: Coronary artery anomalies are characterized by an abnormality in the course or origin of three main coronary arteries. There needs to be more scientific evidence to promptly treat coronary artery anomalies with poorly understood prognostic implications, especially anomalous aortic origin...

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Detalles Bibliográficos
Autores principales: Arun Kumar, Pramukh, Patel, Boskey, Dasari, Mahati, Bhattad, Pradnya Brijmohan, Prabhu, Sushmita, Hadley, Michelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10170789/
https://www.ncbi.nlm.nih.gov/pubmed/37161579
http://dx.doi.org/10.1186/s13256-023-03921-1
Descripción
Sumario:BACKGROUND: Coronary artery anomalies are characterized by an abnormality in the course or origin of three main coronary arteries. There needs to be more scientific evidence to promptly treat coronary artery anomalies with poorly understood prognostic implications, especially anomalous aortic origin of the right coronary artery from the left coronary cusp. CASE PRESENTATION: A 58-year-old Caucasian female presented multiple times over 6 months with atypical chest discomfort and palpitations. The treadmill exercise test demonstrated exercise-induced non-sustained ventricular tachycardia. A coronary angiogram revealed no obstructive coronary artery disease and an anomalous aortic origin of the right coronary artery from the left coronary cusp with an interarterial course. She was managed conservatively with medications, despite persistent recurrent symptoms. CONCLUSION: It is essential to identify subtle symptoms and insidious onset of anomalous aortic origin of the right coronary artery symptoms as seen in our patient, which can contribute to significant morbidity. There are discrepancies in existing guidelines between different cardiovascular societies in managing selected subgroups of patients with anomalous aortic origin of the right coronary artery who do not have high-risk features, but continue to remain symptomatic. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13256-023-03921-1.