Combined Non-Invasive Doppler Echocardiography and Coronary Computed Tomography Lead to Diagnosis of Anomalous Left Coronary Artery From the Pulmonary Artery (ALCAPA) Syndrome.

نویسندگان

  • Kazushi Takemoto
  • Kumiko Hirata
  • Takashi Tanimoto
  • Yoshiki Matsuo
  • Yasushi Ino
  • Takashi Kubo
  • Atsushi Tanaka
  • Takashi Akasaka
چکیده

Received December 18, 2014; revised manuscript received January 17, 2015; accepted January 21, 2015; released online February 19, 2015 Time for primary review: 21 days Division of Cardiology, Department of Medicine, Wakayama Medical University, Wakayama, Japan Mailing address: Kumiko Hirata, MD, Division of Cardiology, Department of Medicine, Wakayama Medical University, 811-1 Kimiidera, Wakayama 641-8509, Japan. E-mail: [email protected] ISSN-1346-9843 doi: 10.1253/circj.CJ-14-1374 All rights are reserved to the Japanese Circulation Society. For permissions, please e-mail: [email protected] Combined Non-Invasive Doppler Echocardiography and Coronary Computed Tomography Lead to Diagnosis of Anomalous Left Coronary Artery From the Pulmonary Artery (ALCAPA) Syndrome

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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-...

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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...

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Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery: The Role of Multislice Computed Tomography (MSCT).

Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital coronary abnormality also known as Bland-White-Garland syndrome. The incidence of ALCAPA is about 1 in every 300,000 live births, and constitutes 0.24% and 0.46% of all congenital cardiac disease. It has a high infant mortality rate reaching up to 90% if left untreated. For many years, the diagn...

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An unusual combination of an anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) and a right coronary artery system with two separate ostia from the aorta in an adult.

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عنوان ژورنال:
  • Circulation journal : official journal of the Japanese Circulation Society

دوره 79 5  شماره 

صفحات  -

تاریخ انتشار 2015