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논문 기본 정보

자료유형
학술저널
저자정보
Sang Bin Bae (Dong-A University) Eun-Ju Kang (Dong-A University College of Medicine) Ki Seok Choo (Pusan National University Yangsan Hospital) Jong-Min Lee (Kyungpook National University) Sang Hyeon Kim (Dong-A University) Kyoung Jae Lim (Dong-A University) Heejin Kwon (Dong-A University)
저널정보
한국심초음파학회 Journal of Cardiovascular Imaging Journal of Cardiovascular Imaging 제30권 제4호
발행연도
2022.10
수록면
231 - 262 (32page)

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There is a wide spectrum of congenital anomalies or variations of the aortic arch, ranging from non-symptomatic variations that are mostly detected incidentally to clinically symptomatic variations that cause severe respiratory distress or esophageal compression. Some of these may be accompanied by other congenital heart diseases or chromosomal anomalies. The widespread use of multidetector computed tomography (CT) in clinical practice has resulted in incidental detection of several variations of the aortic arch in adults. Thus, radiologists and clinicians should be aware of the classification of aortic arch anomalies and carefully look for imaging features associated with a high risk of clinical symptoms. Understanding the embryological development of the aortic arch aids in the classification of various subtypes of aortic arch anomalies and variants. For accurate diagnosis and precise evaluation of aortic arch anomalies, cross-sectional imaging modalities, such as multidetector CT or magnetic resonance imaging, play an important role by providing three-dimensional reconstructed images. In this review, we describe the embryological development of the thoracic aorta and discuss variations and anomalies of the aortic arch along with their clinical implications.

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