Shrivastava Shreya, Joshi Priscilla, Pinglikar Shriyash
Department of Radiodiagnosis, Bharati Vidyapeeth (Deemed to be University), Pune, Maharashtra 411043, India.
BJR Case Rep. 2024 Oct 3;10(5):uaae035. doi: 10.1093/bjrcr/uaae035. eCollection 2024 Sep.
Intramural oesophageal dissection (IED) is an uncommon condition in newborns marked by the separation of the mucosal and submucosal layers of the oesophageal wall, both transversely and longitudinally, which may or may not involve perforation. A neonate presented at 26 h of life with poor respiratory effort and lethargy. She was intubated and was put on mechanical ventilation. Radiograph of the neonate suggested malpositioned endotracheal tube. The fluoroscopic dye-study indicated gastroesophageal oesophageal reflux disease and nothing significant. On limited CT contrast study of thorax, a tubular structure was seen running just parallel to the oesophagus extending from the T2 to the T9 levels. Possibilities of a oesophageal duplication/IED were considered. The neonate underwent an endoscopy and gastrostomy on day of life (DOL) 9. On follow up at 3 months a repeat limited CT study was done with instillation of water-soluble contrast. The previously seen tubular structure running parallel to the oesophagus was no longer seen. This finding suggested a healed IED. This case report emphasizes the significance of multimodality imaging in the diagnosis of this condition.
壁内食管夹层(IED)在新生儿中是一种罕见病症,其特征为食管壁的黏膜层和黏膜下层横向及纵向分离,可能伴有或不伴有穿孔。一名新生儿在出生26小时时出现呼吸费力和嗜睡症状。她接受了插管并进行机械通气。新生儿的X光片显示气管插管位置不当。荧光透视染料研究表明存在胃食管反流病,但无其他明显异常。在胸部有限CT造影研究中,可见一个管状结构与食管平行,从T2延伸至T9水平。考虑了食管重复畸形/IED的可能性。该新生儿在出生第9天接受了内镜检查和胃造口术。在3个月随访时,再次进行有限CT研究并注入水溶性造影剂。之前所见的与食管平行的管状结构不再可见。这一发现提示IED已愈合。本病例报告强调了多模态成像在该病症诊断中的重要性。