Adult-type ALCAPA syndrome: A rare coronary artery anomaly

被引：5

作者：

Patrianakos, Alexandros P. ^{[1
]}

Hatzidakis, Adam ^{[2
]}

Marketou, Maria ^{[1
]}

Parthenakis, Fragiskos I. ^{[1
]}

机构：

[1] Heraklion Univ Hosp, Dept Cardiol, Iraklion, Greece

[2] Heraklion Univ Hosp, Dept Med Imaging, Iraklion, Greece

来源：

ECHOCARDIOGRAPHY-A JOURNAL OF CARDIOVASCULAR ULTRASOUND AND ALLIED TECHNIQUES | 2018年 / 35卷 / 07期

关键词：

2D Echocardiography; anomalous coronary arteries; cardiac imaging; computed tomography; coronary circulation; PULMONARY-ARTERY; ORIGIN; DIAGNOSIS;

D O I：

10.1111/echo.14013

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Anomalous origin of the left coronary artery arising from the pulmonary artery (ALCAPA or Bland-White-Garland syndrome) is a rare but serious congenital coronary artery anomaly, with a poor prognosis without surgical repair. There are two types of ALCAPA syndrome: infant type and adult type. We present a rare case of a 63-year-old female patient, with isolated left anterior descending artery origin from the pulmonary artery. Coronary computed tomography angiography revealed giant and tortuous coronary arteries with many collaterals between the left and right coronary system. The patient refused any surgical treatment.

引用

页码：1056 / 1059

页数：4

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