Congenital atresia of the left main coronary artery associated with patent ductus arteriosus and aortic regurgitation.

نویسندگان

  • Hsin-Hua Chou
  • Chih-Hsiang Chan
  • Kuei-Ton Tsai
  • Chung-I Chang
  • Yu-Lin Ko
چکیده

Congenital left main coronary artery (LMCA) atresia is a rare anomaly and surgical revascularization is recommended once the diagnosis is confirmed. In some cases, LMCA atresia will coexist with other cardiac anomalies, mostly in pediatric patients. A 32-year-old woman had congenital LMCA atresia associated with patent ductus arteriosus (PDA), aortic regurgitation (AR), and moderate pulmonary hypertension. The PDA and AR were repaired surgically and the patient's symptoms improved. Coronary revascularization was not performed because the LCA was supplied by 2 large conus arteries, as "naturally occurring" bypass arteries. The patient remained asymptomatic at the 2.5-year follow-up visit. Given the positive outcome in this patient, surgical repair of the associated cardiac defect without coronary revascularization may be a reasonable approach for patients with congenital LMCA atresia, in which the left coronary arterial tree is supplied by other "naturally occurring" bypass arteries.

برای دانلود رایگان 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

Left-Sided Patent Ductus Arteriosus

W HEN there is a right-sided aortic arch, persistence of a left-sided ductus arteriosus can readily be demonstrated by angiocardiography. This is important because in some types of eyanotic congenital heart disease, such as in the tetralogy of Fallot, anl artificial aortico-pulmonary (Blalock-Taussig' or Pott S2 shunt) is often created in order to alleviate the distress produced by anoxia. Two ...

متن کامل

Aberrant right subclavian artery and right-sided ductus arteriosus.

DESCRIPTION A premature newborn weighing 1.9 kg, presenting with cyanosis, feeding and respiratory difficulties was admitted to our centre for further evaluation. An initial echocardiogram suggested a pulmonary atresia with a malalignment infundibular ventricle septum defect with atypical right-sided ductus arteriosus (2.4 mm) arising from the aberrant right subclavian artery (4 mm), which was ...

متن کامل

Detection of patent ductus arteriosus with intraoperative transesophageal echocardiography in a patient undergoing closure of coronary artery to pulmonary artery fistula

Background Coronary artery to pulmonary artery fistula is an unusual vascular anomaly, and the shunt ratio of this fistula is usually small. Case presentation We report anesthetic management of a 55-year-old female with annuloaortic ectasia, aortic valve regurgitation, and coronary artery to pulmonary artery fistula undergoing radical repair. We calculated the left-to-right shunt ratio after ...

متن کامل

Pulmonary Valve Atresia with Intact Ventricular Septum.

A case of pulmonary valve atresia with intact ventricular septum' with long survival in the absence of a patent ductus arteriosus, is presented. The patient, alive at 21 years of age, has the anterior descending branch of the left coronary artery originating from the pulmonary artery. Thus, the pulmonary blood supply is obtained from the right coronary artery via intercoronary anastomoses. No s...

متن کامل

Bidirectional Cavopulmonary (Glenn) Anastomosis in Pulmonary Atresia with Intact Ventricular Septum and Right Ventricle Dependent Coronary Circulation

This is a case report of an 8-month-old infant with congenital heart disease including; pulmonary atresia, intact ventricular septum, right ventricular hypoplasia, atrial septal defect, coronary sinusoids (fistulas between right ventricle and left anterior descending artery). The patient had a stent for patent ductus arteriosus at 3 months of age and after 4 months a bidirectional Glenn shunt o...

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

عنوان ژورنال:
  • The American journal of medicine

دوره 50 3  شماره 

صفحات  -

تاریخ انتشار 1971