Di Mitri Marco, Coletta Riccardo, Collautti Edoardo, Bisanti Cristian, Di Carmine Annalisa, Lo Piccolo Roberto, Rovero Elena, Tocchioni Francesca, Severi Elisa, Moroni Marco, Georgopoulos Ioannis, Patkowski Dariusz, Lima Mario
Pediatric Surgery Department, Meyer Children's Hospital IRCCS, 50139 Firenze, Italy.
Alma Mater Studiorum, University of Bologna, 40126 Bologna, Italy.
Children (Basel). 2025 Jun 6;12(6):740. doi: 10.3390/children12060740.
Esophageal atresia (EA) type A, characterized by the absence of a tracheoesophageal fistula and typically presenting with a long esophageal gap, usually requires staged repair. We report a rare case of a newborn with type A EA in which both the proximal and distal esophageal pouches were unexpectedly close and located in the cervical region. This anatomical variant allowed for a successful primary anastomosis through a cervical approach. Initial imaging was misleading, and the true anatomy was clarified only through thoracoscopic exploration, underscoring the importance of intraoperative flexibility. To our knowledge, this is the first report of such a presentation in type A EA, with significant implications for diagnosis and surgical strategy.
A型食管闭锁(EA)的特征是没有气管食管瘘,通常表现为食管间隙长,通常需要分期修复。我们报告了一例罕见的A型EA新生儿病例,其近端和远端食管囊袋意外靠近且位于颈部区域。这种解剖变异使得通过颈部入路成功进行了一期吻合。最初的影像学检查有误导性,只有通过胸腔镜探查才明确了真实的解剖结构,强调了术中灵活性的重要性。据我们所知,这是A型EA中这种表现的首次报告,对诊断和手术策略具有重要意义。