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이중대동맥궁으로 인한 호흡곤란 1례

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Author(s)
최용식김덕준손영탁송달원
Keimyung Author(s)
Kim, Deok JunSohn, Young TakSong, Dal Won
Department
Dept. of Otorhinolaryngology (이비인후과학)
Journal Title
대한기관식도과학회지
Issued Date
1995
Volume
1
Issue
1
Abstract
Double aortic arch is the most common among vascular structure anomalies in infancy. It's clinical manifestations vary from incidental discovery without symptoms to symptoms of tracheal or esophageal compression such as stridor, wheezing, excessive secretion, dyspnea and dysphagia. Characteristically many patients show little sign of respiratory difficulty during sleep and quiet monents but this symptom is frequently exacerbated by crying or exertion, which may be difficult to distinguish from bronchial asthma. CT and MRI are believed to be the most valuable methods of diagnosis and surgical intervention is necessary in severe cases. Recently, we experienced a case of dyspnea due to double aortic arch. So we report this case with review of literatures.
Alternative Title
A Case of Dyspnea due to Double Aortic Arch
Keimyung Author(s)(Kor)
김덕준
손영탁
송달원
Publisher
School of Medicine
Citation
최용식 et al. (1995). 이중대동맥궁으로 인한 호흡곤란 1례. 대한기관식도과학회지, 1(1), 159–163.
Type
Article
ISSN
1226-0916
URI
https://kumel.medlib.dsmc.or.kr/handle/2015.oak/37680
Appears in Collections:
1. School of Medicine (의과대학) > Dept. of Otorhinolaryngology (이비인후과학)
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