查詢結果分析
相關文獻
- Usefulness of Multidetector-row Computed Tomography in Diagnosis of Anomalous Origin of Left Coronary Artery Arising From the Pulmonary Artery
- The Significance of Early Subtle Coronary Arterial Lesions on Echocardiogram in Kawasaki Disease
- Fatal Pulmonary Embolism in a Child Undergoing Extra-Ventricular Drainage Surgery--A Case Report
- Midterm Outcome of Mitral Valve Regurgitation after Repair of Atrioventricular Septal Defect
- 影像分析及計算機圖學應用於心臟超音波
- Pulmonary Hypertension--From Echocardiography and Electrocardiography to Clinical Correlation
- Hypereosinophilic Syndrome--A Case Report
- Tuberculous Pericardial Effusion with Intrapericardial Echogenic Masses-- A Case Report
- Changes of Endothelin-1 and Atrial Natriuretic Peptide during Dobutamine Stress Echocardiography
- Multiplane Transesophageal Echocardiography in the Diagnosis of Sinus Venosus Atrial Septal Defect in Adults
頁籤選單縮合
題名 | Usefulness of Multidetector-row Computed Tomography in Diagnosis of Anomalous Origin of Left Coronary Artery Arising From the Pulmonary Artery=利用多層螺旋電腦斷層影像診斷左冠狀動脈起源於肺動脈症 |
---|---|
作者姓名(中文) | 蘇界守; 蔡依橙; 林維文; 林芳宜; 丁紀台; 王國陽; | 書刊名 | Journal of the Chinese Medical Association |
卷期 | 73:9 2010.09[民99.09] |
頁次 | 頁492-495+CA88 |
關鍵詞 | 左冠狀動脈起源於肺動脈症; 心臟超音波; 多層螺旋電腦斷層影像; ALCAPA syndrome; Echocardiography; Multidetector-row computed tomography; |
語文 | 英文(English) |
英文摘要 | Anomalous origin of the left coronary artery arising from the pulmonary artery (ALCAPA) is a rare congenital heart defect that affects approximately 1 in 300,000 live births and accounts for 0.5% of all congenital heart disease. Without surgical intervention, most patients with this anomaly die in infancy. The diagnosis of ALCAPA syndrome is sometimes difficult, especially in children, because it often presents with atypical symptoms and signs. Echocardiography can yield some findings that are highly indicative of this syndrome. Cardiac catheterization usually establishes the diagnosis, but it is invasive and painful. Multidetector-row computed tomography (MDCT) is a valuable alternative tool to confirm the diagnosis of ALCAPA syndrome. In this report, we describe a 24-year-old woman with a dilated right coronary artery detected by transthoracic echocardiography, showing an interventricular abnormal flow over the diastolic phase of the cardiac cycle and the left main coronary artery not merging with the ascending aorta. The diagnosis of ALCAPA syndrome was confirmed by MDCT. |
本系統之摘要資訊系依該期刊論文摘要之資訊為主。