Division of Thoracic Surgery, Department of Surgery, New York Presbyterian Hospital and Columbia University, New York, NY, USA.
Division of Pediatric Surgery, Department of Surgery, New York Presbyterian Hospital and Columbia University, New York, NY, USA.
Eur J Cardiothorac Surg. 2017 Dec 1;52(6):1218-1222. doi: 10.1093/ejcts/ezx164.
Recurrent congenital tracheoesophageal fistula (TEF) is well documented in infancy but may also present later in life. This study reviews our experience with the clinical presentation, diagnosis and management of 5 recurrent and 2 primary congenital tracheoesophageal fistulas (TEF) in adult patients. There are no literature series of late recurrence of TEF (repaired in childhood and recurring in adulthood) and relatively few reported cases of initial adult presentation of TEF. In this series, we aim to provide the first large series description of late recurrence of congenital TEF following repair in infancy or childhood. We also present management considerations for this unique group of patients.
We performed a computer-based search of the adult thoracic surgery departmental operative database at our institution from 2002 to 2014. Patients with iatrogenic TEF or malignant TEF were excluded.
Seven patients are included in our series. Five patients (71%) had recurrent congenital TEF and 2 (29%) had initial diagnosis of congenital TEF. All presented with severe coughing symptoms, and most (86%) had a history of recurrent aspiration pneumonia. Repair technique was dictated by the location of the TEF and the specific tracheoesophageal pathology. Four patients underwent repair via cervical approach with or without a tracheal resection. Three patients with distal recurrence underwent repair via right thoracotomy with partial oesophagectomy for significant tissue compromise and cervical reconstruction. Patients were followed for at least 1 year. All 7 patients experienced full resolution of symptoms. One patient required postoperative placement of a retrievable tracheal stent for tracheomalacia. There were no mortalities.
Adult presentation of congenital TEF is a rare but recognizable clinical entity. Recurrent TEF in adulthood is a possible late complication of TEF repair performed in childhood that has not previously been described. Adult patients experiencing symptoms of cough and recurrent aspiration pneumonia should be evaluated for congenital TEF. Surgical repair of congenital TEF in the adult is feasible and effective with acceptable morbidity.
复发性先天性气管食管瘘(TEF)在婴儿期已有充分记录,但也可能在以后的生活中出现。本研究回顾了我们在 5 例复发性和 2 例原发性先天性气管食管瘘(TEF)成年患者的临床表现、诊断和治疗方面的经验。目前尚无关于 TEF 晚期复发(儿童期修复后复发)的文献系列,且最初表现为成人 TEF 的病例相对较少。在本系列中,我们旨在首次对儿童期修复后复发性先天性 TEF 进行大系列描述。我们还为这组独特的患者提供了治疗管理方面的考虑。
我们对我院 2002 年至 2014 年成人胸外科手术部门操作数据库进行了计算机检索。排除医源性 TEF 或恶性 TEF 患者。
本系列纳入 7 例患者。5 例(71%)患者患有复发性先天性 TEF,2 例(29%)患者为先天性 TEF 初诊。所有患者均表现为严重咳嗽症状,且大多数(86%)有反复吸入性肺炎史。修复技术由 TEF 的位置和特定的气管食管病理决定。4 例患者经颈侧入路修复,伴或不伴气管切除术。3 例远端复发患者经右胸入路行部分食管切除术,因严重组织损伤而行颈重建术。所有患者的随访时间至少为 1 年。7 例患者的症状均完全缓解。1 例患者因气管软化需术后放置可回收气管支架。无死亡病例。
成人先天性 TEF 的表现是一种罕见但可识别的临床实体。儿童期 TEF 修复后成年期出现复发性 TEF 是一种以前未描述的可能的晚期并发症。出现咳嗽和反复吸入性肺炎症状的成年患者应评估是否存在先天性 TEF。成人先天性 TEF 的手术修复是可行且有效的,其发病率可接受。