Article Text

Download PDFPDF
CASE REPORT
Anomalous origin of the right coronary artery with concomitant myxomatous mitral valve disease: a rare coexistence
  1. Yoichi Imori,
  2. Masato Murakami,
  3. Masashi Tanaka,
  4. Shigeru Saito
  1. Department of Cardiovascular Medicine, Shonan Kamakura General Hospital, Kanagawa, Japan
  1. Correspondence to Dr Yoichi Imori, yoichiimori{at}me.com

Summary

A 45-year-old man previously diagnosed with myxomatous mitral valve disease was admitted to our hospital with chest pain at rest and on effort. Contrast-enhanced CT revealed that the patient's right coronary artery originated from the left sinus Valsalva, which was compressed between the aortic and pulmonary roots. This anatomical abnormality can be associated with sudden death, syncope and chest pain. Ultrasonography showed mitral valve prolapse with severe regurgitation. Surgical repair was performed, which included coronary artery bypass graft and mitral valvoplasty with tricuspid annuloplasty. The postoperative course was uneventful and the patient remains asymptomatic. This is the first description of the coexistence of an anomalous origin of the right coronary artery with myxomatous mitral valve disease.

Statistics from Altmetric.com

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.