Harrison Ciara, Harrison Jo, Fricke Tyson A, Konstantinov Igor E
Department of Respiratory Medicine, Royal Children's Hospital, Melbourne, Australia.
Department of Cardiothoracic Surgery, Royal Children's Hospital, Melbourne, Australia.
Interdiscip Cardiovasc Thorac Surg. 2024 Sep 4;39(3). doi: 10.1093/icvts/ivae152.
Infant long-segment congenital tracheal stenosis (LTS) is rare and presents a challenging clinical scenario. We describe the management of a child who required extracorporeal membrane oxygenation following a respiratory arrest and underwent slide tracheoplasty in infancy for severe LTS and required repeated bronchoscopic reinterventions for recurrent tracheal granulations. At 9 years of age, the child has normal pulmonary function testing and a normal exercise tolerance.
婴儿长段先天性气管狭窄(LTS)较为罕见,呈现出具有挑战性的临床情况。我们描述了一名儿童的治疗过程,该儿童在呼吸骤停后需要体外膜肺氧合,并在婴儿期因严重LTS接受了滑动气管成形术,且因复发性气管肉芽组织需要反复进行支气管镜再次干预。9岁时,该儿童的肺功能测试正常,运动耐量也正常。