Anomalous origin of left coronary artery from innominate artery.

نویسندگان

  • Yang Min Kim
  • Rak Kyeong Choi
  • Chang Keun Lee
چکیده

rom the Departments of Radiology and †Internal edicine, Sejong Hospital nd Sejong Heart Institute, yunggi, South Korea. anuscript received anuary 21, 2009; ccepted February 6, 2009. A78-year-old woman was admitted with chest pain. Coronary angiography revealed a normal right coronary artery. The left coronary artery (LCA) could not be intubated and was not possible to demonstrate on right coronary angiography or root aortography. On electrocardiography-gated 64-slice computed tomography coronary angiography, there was neither coronary artery nor any dimpling originating from the left sinus of Valsalva. The LCA (arrows) was arising from the right innominate artery (IA), going along with the ascending aorta (AA), eventually reaching its normal position (A to C, Online Video). The Online Video of axial computed tomography images reveals the entire course of the anomalous artery. On second coronary angiography, the anomalous origin of the LCA from the IA was confirmed (D). This patient had no history of previous thoracic surgery. Anomalous coronary artery almost exclusively originates from an inappropriate aortic sinus of Valsalva or pulmonary artery. In the patient with aortic atresia, the diminutive ascending aorta seemingly terminates in the coronary artery, being misjudged as a tributary of the IA (1). To the best of our knowledge, there has been no report of this anomaly in the absence of aortic atresia. ublished by Elsevier Inc. doi:10.1016/j.jacc.2009.02.070

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Different Presentation of Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery in Adults: Case Reports

Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital cardiac malformation. We report three cases of ALCAPA who survived to adulthood. The first case was a 51-year-old woman who complained of typical chest pain that was diagnosed with ALCAPA using cardiac catheterization and coronary computed tomographic angiography (CTA). The second case was a 30-...

متن کامل

The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA): a Case Series and Brief Review

Background Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital cardiovascular defect that occurs in approximately 1/300 000 live births or 0.5% of children with congenital heart disease. There are two types of ALCAPA syndrome: the infant type and the adult type. The most infants experience myocardial infarction and congestive heart failure, and approximately 9...

متن کامل

CongenItal Anomallous Origin of Left Anterior Descending Artery from RIight Coronary Artery

​Congenital anomalies of the coronary arteries have been a known subject  since the advent of cardiac angiography, and has been a subject of special interest by both cardiologists and cardiac surgeons,  We have tried in this article to present a case of anomalous origin of LAD from RCA (RMT) in a 55 year old lady (Mrs. B.J.) and to completely dis­cuss this subject. It's worthmentioning that thi...

متن کامل

Congenital Absence of Left Circumflex Coronary Artery

Congenital absence of left circumflex artery is a rare congenital anomaly of the coronary arteries. The prevalence of the anomaly in different studies ranges from 0.6% to 1.3%. Of these, 80% are benign and asymptomatic and 20% are clinically important. We report a 56-year-old man presented with acute resting chest pain who was diagnosed as having acute anterolateral infarction accompanied by el...

متن کامل

Clinical Implications of Congenital Absence of Circumflex Coronary Artery

Introduction: Coronary artery anomalies are rare clinical entities reported in 0.6% to 5.6% of diagnostic coronary angiographies. Anomalous origins of coronary arteries from distal segments are rarely reported. Presented herein is a coronary anomaly in which the circumflex artery (CX) originated as a continuation of the posterolateral branch of the right coronary artery (RCA) w...

متن کامل

گزارش یک مورد بیماری ایسکمیک شدید قلبی در شیرخوار سه ماهه ناشی از منشاء گیری نابجای شریان کرونری چپ از تنه شریان ریوی، ارجاعی به سالن تشریح پزشکی قانونی تبریز

 Detection of causes of sudden natural death is a major problem of physicians and exact inspection of rare causes of sudden death reduces numbers of white autopsies and helps to well performance of justice. Anomalous origin of coronary arteries are one of These rare cases that mostly in infants leading to death due to Ischemia and heart failure , and sometimes survive until Adulthood and attent...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Journal of the American College of Cardiology

دوره 54 2  شماره 

صفحات  -

تاریخ انتشار 2009