| Literature DB >> 22843914 |
Naoshi Kubo1, Masaichi Ohira, Yoshito Yamashita, Katsunobu Sakurai, Hiroaki Tanaka, Kazuya Muguruma, Kenjiro Kimura, Hisashi Nagahara, Eiji Noda, Ryosuke Amano, Masakazu Yashiro, Kiyoshi Maeda, Kosei Hirakawa.
Abstract
Double aortic arch (DAA) is an extremely rare vascular malformation which causes tracheal and esophageal compression, resulting in respiratory symptoms such as stridor and wheezing, or feeding problems such as dysphagia, usually during the first few months of life. In contrast, this disorder is rarely diagnosed in adults. We herein present an elderly case with thoracic esophageal carcinoma with DAA. To the best of our knowledge, this is only the second report of a successfully resected case of esophageal cancer associated with DAA in the English literature. Moreover, this is the first reported case of symptomatic DAA with esophageal carcinoma. Spiral computed tomography and three-dimensional reconstruction was very useful for preoperative assessment of the abnormal vessels.Entities:
Mesh:
Year: 2012 PMID: 22843914
Source DB: PubMed Journal: Anticancer Res ISSN: 0250-7005 Impact factor: 2.480