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A case of right ductus and left innominate artery from the pulmonary trunk
Author(s) -
Tran Vinh Quang,
Nguyen Truong Ly Thinh,
Nguyen Mai Tuan,
Luong Canh Minh,
Dinh Duyen Mai,
Vuong Anh Doan
Publication year - 2020
Publication title -
asian cardiovascular and thoracic annals
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.203
H-Index - 27
eISSN - 1816-5370
pISSN - 0218-4923
DOI - 10.1177/0218492319865425
Subject(s) - medicine , aortic arch , intracardiac injection , ductus arteriosus , digeorge syndrome , interrupted aortic arch , cardiology , left pulmonary artery , trunk , atrioventricular cushions , double aortic arch , atresia , right pulmonary artery , truncus arteriosus , pulmonary artery , surgery , heart disease , aorta , tetralogy of fallot , psychiatry , ecology , biology
Right-sided aortic arch is a rare anatomic variation of aortic arch anomaly, which may coexist with or without other cardiac defects. We report an extremely rare case of right-sided aortic arch with a right ductus arteriosus and isolation of the left brachiocephalic trunk, without other associated intracardiac lesions. We describe the successful surgical management of this anomaly in a neonate who had bilateral choanal atresia without DiGeorge syndrome or Down syndrome. However, our patient had clinical signs of hearing loss in the postoperative follow-up period.

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