Bielecka-Dabrowa Agata, Bikiewicz Agata, Rybak Marek, Pawliczak Filip, Lewek Joanna, Banach Maciej, Maciejewski Marek
Department of Preventive Cardiology and Lipidology, Chair of Nephrology and Hypertension Medical University of Lodz Lodz Poland.
Polish Mother's Memorial Hospital Research Institute (PMMHRI) Department of Cardiology and Congenital Diseases of Adults Lodz Poland.
Clin Case Rep. 2021 Dec 6;9(12):e05085. doi: 10.1002/ccr3.5085. eCollection 2021 Dec.
The Taussig-Bing anomaly is a rare cyanotic congenital heart defect treated surgically in the early infancy. The preferred repair procedure is an arterial switch operation combined with ventricular septal defect closure. Despite promising long-term functional outcomes and survival benefits, neo-aortic dysfunction and arrhythmias might be relevant complications.
陶西格-宾畸形是一种罕见的青紫型先天性心脏病,在婴儿早期进行手术治疗。首选的修复手术是动脉调转术联合室间隔缺损闭合术。尽管有良好的长期功能预后和生存益处,但新主动脉功能障碍和心律失常可能是相关并发症。