Department of Respiration, Shanghai Children's Medical Center, Shanghai, PR China.
Pediatr Pulmonol. 2010 Sep;45(9):945-7. doi: 10.1002/ppul.21235.
Congenital tracheal web is a very rare abnormality that often manifests as wheezing, dyspnea, and respiratory failure. Misdiagnosis is common. Here we describe the case of a 47-day-old female infant who presented after severe, extended coughing. The diagnosis of congenital tracheal web was made following coronal computer tomography (CT) reconstruction and bronchoscopy. The bronchoscope was used to facilitate tracheal expansion. This is the youngest case reported to date to highlight the diagnosis and treatment of a 47 days infant with congenital tracheal web. An infant with tracheal web, a very rare congenital anomaly can be clearly diagnosed by coronal CT reconstruction combined with bronchoscopy. If diagnosed early, the bronchoscope may be used to facilitate tracheal expansion.
先天性气管蹼是一种非常罕见的异常,常表现为喘息、呼吸困难和呼吸衰竭。误诊很常见。我们在此描述一例 47 天大的女婴,因剧烈、持续咳嗽就诊。冠状位计算机断层扫描(CT)重建和支气管镜检查后诊断为先天性气管蹼。支气管镜用于促进气管扩张。这是目前报道的年龄最小的病例,旨在强调对 47 天婴儿先天性气管蹼的诊断和治疗。冠状位 CT 重建结合支气管镜检查可明确诊断气管蹼这种非常罕见的先天性异常。如果早期诊断,支气管镜可用于促进气管扩张。