Fukuzawa Hiroaki, Okamoto Mitsumasa, Tsuruno Yudai, Maruo Ayako
Department of Pediatric Surgery, Japanese Red Cross Society Himeji Hospital, 1-12-1 Shimoteno, Himeji, Japan.
Department of Cardiovascular Surgery, Kakogawa City Hospital, Kakogawa, Japan.
Surg Case Rep. 2022 Sep 8;8(1):165. doi: 10.1186/s40792-022-01523-5.
Repair of esophageal atresia is usually performed through the right thoracic cavity. However, when the upper pouch of the esophagus and tracheoesophageal fistula (TEF) is located in the thoracic inlet and completely on the left side of trachea, it is difficult to dissect and anastomose the esophagus through the right thoracic cavity. We present a case of esophageal atresia, with the esophageal upper pouch located high and completely on the left side of trachea, successfully repaired via the median sternotomy approach.
A male neonate with a birth weight of 1766 g was prematurely delivered via cesarean section at 34 weeks of gestation. Contrast-enhanced computed tomography (CT) showed that the upper pouch of the esophagus was located at the thoracic inlet and completely on the left side of the trachea; hence, a diagnosis of esophageal atresia was made. Moreover, a TEF was connected to the trachea at the level of the lower end of the upper esophageal pouch. An aberrant right subclavian artery and persistent left superior vena cava were also detected. Esophageal dissection and anastomosis were determined to be very difficult if approached from the right thoracic cavity. Therefore, we performed median sternotomy one day after the neonate was born. The upper pouch of the esophagus and TEF were easily dissected via the median sternotomy approach. Anastomosis of the esophagus was performed, with a good visual field, to the left of the trachea. The postoperative course was uneventful.
This is the first reported case of a median sternotomy approach for esophageal atresia. This technique may be useful when a right thoracic approach is difficult, especially if the esophageal upper pouch is located completely to the left of the trachea or if it is higher than the normal position.
食管闭锁修复术通常经右胸腔进行。然而,当食管上段囊袋和气管食管瘘(TEF)位于胸廓入口且完全在气管左侧时,经右胸腔难以对食管进行解剖和吻合。我们报告1例食管闭锁病例,其食管上段囊袋位置高且完全在气管左侧,经正中胸骨切开术成功修复。
1例出生体重1766g的男性新生儿,孕34周剖宫产早产。增强计算机断层扫描(CT)显示食管上段囊袋位于胸廓入口且完全在气管左侧,因此诊断为食管闭锁。此外,在食管上段囊袋下端水平有一TEF与气管相连。还检测到右锁骨下动脉异常和永存左上腔静脉。若经右胸腔入路,食管解剖和吻合将非常困难。因此,在新生儿出生后1天实施了正中胸骨切开术。经正中胸骨切开术很容易解剖食管上段囊袋和TEF。在气管左侧视野良好的情况下进行了食管吻合。术后过程顺利。
这是首例报道的采用正中胸骨切开术治疗食管闭锁的病例。当右胸入路困难时,尤其是食管上段囊袋完全位于气管左侧或高于正常位置时,该技术可能有用。