Department of Surgery, University of Mississippi Medical Center, Jackson, MS, USA.
Department of Pediatric Surgery, University of Mississippi Medical Center, Jackson, MS, USA.
Am Surg. 2024 Aug;90(8):2089-2091. doi: 10.1177/00031348241241749. Epub 2024 Mar 28.
Tracheoesophageal fistula (TEF) and esophageal atresia (EA) are rare congenital anomalies occurring in approximately 1 in 2500 to 3500 neonates. We present a neonatal patient diagnosed with EA/TEF in conjunction with pulmonary agenesis requiring definitive repair via median sternotomy. The child was born at 33 weeks gestational age with post-delivery respiratory distress necessitating intubation. A nasogastric tube was unable to be passed. After subsequent imaging, TEF and pulmonary agenesis were diagnosed. During planned staged repair with ligation of TEF via standard right thoracotomy approach, significant ventilatory compromise was encountered. Due to concern for ventilatory compromise and anatomical variance limiting visualization, a median sternotomy approach was utilized for definitive repair. This exposure and repair were successful and may be considered for cases with complex pulmonary malformation limiting standard thoracotomy. To our knowledge, this is only the second reported case of a successful TEF/EA repair using a median sternotomy approach.
食管气管瘘(TEF)和食管闭锁(EA)是罕见的先天性畸形,在大约 2500 至 3500 名新生儿中发生 1 例。我们报告了 1 例新生儿患者,该患者被诊断为 EA/TEF 合并肺发育不全,需要通过正中胸骨切开术进行确定性修复。该患儿在 33 孕周时出生,出生后出现呼吸窘迫,需要插管。无法通过鼻胃管。随后进行影像学检查,诊断为 TEF 和肺发育不全。在计划的分期修复中,通过标准右开胸术结扎 TEF 时,出现了明显的通气障碍。由于担心通气障碍和解剖变异限制了可视化,因此采用了正中胸骨切开术进行确定性修复。该暴露和修复是成功的,对于复杂的肺部畸形限制了标准开胸术的病例,可以考虑这种方法。据我们所知,这是仅有的第二例使用正中胸骨切开术成功修复 TEF/EA 的报道病例。