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題 名 | An Adult with Aortic Arch Interruption Associated with Sinus Venosus Atrial Septal Defect and Partial Anomalous Pulmonary Venous Connection=一位成年人之主動脈截斷合併靜脈竇型心房中膈缺損及部分肺靜脈連結異常 |
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作 者 | 謝育整; 吳茲睿; 王國陽; 梁凱偉; 林維文; 陳穎行; 丁紀台; | 書刊名 | 中華醫學會雜誌 |
卷 期 | 70:1 2007.01[民96.01] |
頁 次 | 頁30-32+CA5 |
分類號 | 416.26 |
關鍵詞 | 心房中膈缺損; 主動脈截斷; 部分肺靜脈連結異常; |
語 文 | 英文(English) |
中文摘要 | 主動脈截斷是一種少見而致命性的先天性疾病,且常合併多動的心臟血管畸形。大部分患有主動脈截斷的新生兒在出生後當肺動脈導管關閉時,就會造成死亡。然而,卻有少數病患可以順利地存活至成年。我們報告一位十九歲男性因持續三個月的運動性氣促來就診,一系列的心臟血管檢查後確認此病患患有主動脈截斷合併靜脈竇型心房中隔缺損及部分肺靜脈連結異常。就我們所知,這種複雜性的先天異常未曾在成年人被報告過。 |
英文摘要 | Interruption of the aortic arch is a rare and usually lethal congenital anomaly that is often associated with multiple cardiac malformations. Most neonates with aortic arch interruption perish once the ductus arteriosus closes after birth. However, sporadic cases have been reported to survive into adulthood uneventfully. Here, we report a 19-year-old male with a 3-month history of exertional dyspnea. A series of cardiovascular studies confirmed the presence of aortic arch interruption in conjunction with sinus venosus atrial septal defect and partial anomalous pulmonary venous connection. To the best of our knowledge, such an association has not been previously reported in adults. |
本系統中英文摘要資訊取自各篇刊載內容。