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Congenital Absence of the Right Coronary Artery: A Case Report and Literature Review

Overview
Specialty General Medicine
Date 2018 Mar 22
PMID 29561437
Citations 11
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Abstract

Rationale: Congenital absence of the right coronary artery (RCA) is a rare congenital malformation of the cardiovascular system which may have fatal consequences.

Patient Concerns: A 63-year-old man with a 5-year history of chest pain after exertion which had aggravated for >1 month was advised for admission and computed tomography angiography (CTA) examination of the coronary artery to screen for coronary artery disease (CAD).

Diagnoses: The coronary artery CTA showed absence of RCA arising form the aortic root after which a selective coronary angiography (SCA) examination was done that confirmed the diagnosis of congenital absence of RCA.

Interventions: As the patient refused to receive a coronary artery stent implantation citing his financial condition, only symptomatic treatment was given.

Outcomes: The patient requested to be discharged from the hospital against the advice of his doctors 1 week later. A query made by the telephone suggested that the patient's symptoms were under control by use of prescribed medications only.

Lessons: Although being a rare condition, a coronary artery CTA examination can be utilized to screen for congenital absence of RCA and other varieties of cardiovascular malformation whereas SCA can be performed to confirm the diagnosis.

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References
1.
Desmet W, Vanhaecke J, Vrolix M, Van de Werf F, Piessens J, Willems J . Isolated single coronary artery: a review of 50,000 consecutive coronary angiographies. Eur Heart J. 1992; 13(12):1637-40. DOI: 10.1093/oxfordjournals.eurheartj.a060117. View

2.
SANDISON A . Congenital absence of the right coronary artery: with report of a case in a coalminer with gross hypertrophy of the right ventricle. Glasgow Med J. 1955; 36(10):343-7. PMC: 5977901. View

3.
Kervancioglu M, Tokel K, Varan B, Yildirim S . Frequency, origins and courses of anomalous coronary arteries in 607 Turkish children with tetralogy of Fallot. Cardiol J. 2011; 18(5):546-51. DOI: 10.5603/cj.2011.0011. View

4.
Aydinlar A, Cicek D, Senturk T, Gemici K, Serdar O, Kazazoglu A . Primary congenital anomalies of the coronary arteries: a coronary arteriographic study in Western Turkey. Int Heart J. 2005; 46(1):97-103. DOI: 10.1536/ihj.46.97. View

5.
Li S, Ni Q, Wu H, Peng L, Dong R, Chen L . Diagnostic accuracy of 320-slice computed tomography angiography for detection of coronary artery stenosis: meta-analysis. Int J Cardiol. 2013; 168(3):2699-705. DOI: 10.1016/j.ijcard.2013.03.023. View