Abstract
Taussig–Bing anomaly is rare congenital heart malformation relating to a group characterized by the aorta and the pulmonary artery beginning
from the right ventricle with ventricular septal defect.
Anatomic correction of Taussig–Bing anomaly is characterized by a wide variety of surgical approaches, depending on the anatomical variants
of the defect. Currently, the surgery of choice is arterial switch with ventricular septal defect plasty. The combination of Taussig–Bing anomaly
with other congenital heart defects is extremely rare, and each patient is the subject of a separate discussion. We present a case of successful
correction of Taussig–Bing anomaly with type B interrupted aortic arch.
References
1. Бураковский В.И., Бокерия Л.А. (ред.) Сердечно-сосудистая хирургия: руководство. М.: Медицина; 1996.
2. Agematsu K., Aoki M., Naito Y., Fujiwara T. Surgical palliation for taussig-bing anomaly with multiple lesions. Asian Cardiovasc. Thorac.
Ann. 2008; 16: 412–3.
3. Hubera C., Mimicb B., Oswalb N. et al. Outcomes and re-interventions after one-stage repair of transposition of great arteries and aortic
arch obstruction. 23rd Annual Meeting of the European Association for Cardio-thoracic Surgery, Vienna, Austria, October 18–21, 2009.
4. Lacour-Gayet F. Arterial switch operation with ventricular sepatiental defect repair and aortic arch reconstruction. Semin. Thorac.
Cardiovasc. Surg. 2007; 19: 245–8.
5. Mavroudis C. Pediatric cardiac surgery. Mosby; 2003: 415.
