Sengupta Aditya, Murthy Raghav A, Pastuszko Peter
Department of Cardiovascular Surgery, The Mount Sinai Hospital, New York, NY, USA.
Division of Pediatric Cardiac Surgery, Department of Cardiovascular Surgery, The Mount Sinai Hospital, New York, NY, USA.
Transl Pediatr. 2021 Feb;10(2):454-458. doi: 10.21037/tp-20-174.
The previously unreported case of a child with an exceedingly rare amalgamation of complex defects, including truncus arteriosus (TA), double aortic arch (DAA), tracheoesophageal fistula, and choanal atresia is presented. First, on day-of-life (DOL) 2, with a joint effort involving Pediatric Cardiac Surgery, General Surgery, and Otolaryngology, division of tracheoesophageal fistula and repair of esophageal atresia, along with choanal atresia repair, was carried out. Via a right thoracotomy, the tracheoesophageal fistula, located medial to the azygous vein, was skeletonized and ligated. The proximal esophagus was then mobilized up to the thoracic inlet as it coursed through the vascular ring. This enabled esophageal anastomosis with preservation of both aortas. Next, on DOL 11, the child underwent TA repair. Following a standard midline sternotomy and cooling to moderate hypothermia, the left aortic arch was divided and oversewn. The aorta was then transected anteriorly, and the main pulmonary artery (MPA) exiting the posterior aorta was harvested as a single button. The aortic defect from the pulmonary artery button was repaired with autologous pericardium. Next, through a right ventriculotomy, the previously seen conoventricular septal defect was identified and closed. Finally, a 10-mm pulmonary homograft was anastomosed to the pulmonary artery bifurcation to complete the repair. The patient was discharged on DOL 78 and was noted to be doing well at 1-year follow-up. This case validates the feasibility of fistula repair complicated by DAA through a right thoracotomy, the durability of staged, complete repair of TA and DAA, and the advantages of a holistic, team-based approach that optimizes timing of all repairs based upon a careful consideration of the exponential, rather than additive, effects of multi-organ disease on post-cardiac surgery outcomes in neonates.
本文介绍了一例此前未报道的儿童病例,该患儿患有极为罕见的复杂缺陷合并症,包括永存动脉干(TA)、双主动脉弓(DAA)、气管食管瘘和后鼻孔闭锁。首先,在出生后第2天(DOL 2),在小儿心脏外科、普通外科和耳鼻喉科的共同努力下,进行了气管食管瘘分离和食管闭锁修复,以及后鼻孔闭锁修复。通过右胸切口,将位于奇静脉内侧的气管食管瘘进行骨骼化并结扎。然后,随着近端食管穿过血管环,将其向上游离至胸廓入口。这样就能够在保留双主动脉的情况下进行食管吻合。接下来,在DOL 11,患儿接受了TA修复。经过标准的正中胸骨切开术并降温至中度低温后,将左主动脉弓切断并缝合。然后在前方横断主动脉,将从后主动脉发出的主肺动脉(MPA)作为一个单一的纽扣状组织取下。用自体心包修复肺动脉纽扣状组织造成的主动脉缺损。接下来,通过右心室切开术,识别并关闭先前发现的圆锥室间隔缺损。最后,将一个10毫米的肺动脉同种异体移植物吻合到肺动脉分叉处,完成修复。患儿于DOL 78出院,在1年随访时情况良好。该病例证实了通过右胸切口修复合并DAA的瘘管的可行性、分期完全修复TA和DAA的耐久性,以及基于整体、团队的方法的优势,该方法基于仔细考虑多器官疾病对新生儿心脏手术后结果的指数而非累加效应来优化所有修复的时机。