Delayed Diagnosis of Bilateral Congenital Choanal Obstruction in a 4-Year-Old Girl: Transnasal Repair with Temporary Stenting and Short-Term Outcome: A Case Report.
Abdulle Zakarie Abdijamal ZA, Mohamud Mohamed Abdirahman MA, Alpha Muhindo Kavuyiro MK, Mohamed Mohamed Ibrahim MI et al.
Choanal atresia is a rare congenital cause of nasal obstruction. Complete obstruction is termed atresia, whereas partial narrowing is more accurately described as choanal stenosis. We report a 4-year-old girl with lifelong bilateral nasal obstruction, persistent mouth breathing, snoring, poor sleep, easy tiredness, intermittent rhinorrhoea, breastfeeding difficulty during infancy, and recurrent respiratory tract infections. Clinical assessment showed absent right-sided and markedly reduced left-sided nasal airflow. Bedside testing demonstrated no right-sided cotton-wisp movement or misting and minimal movement and misting on the left; a size 8F suction catheter could not be advanced beyond 3.5 cm on the right and met posterior resistance on the left. Preoperative flexible nasal endoscopy was not obtained because financial constraints limited access to the procedure. Computed tomography demonstrated complete right-sided choanal atresia with incomplete left-sided congenital choanal stenosis. The child underwent transnasal repair under general anesthesia using direct visualization with a Killian nasal speculum and headlight, puncture and serial dilatation of the posterior choanal obstruction, and temporary bilateral stenting. The stents were removed after six weeks. During four weeks of follow-up after stent removal, the child had improved nasal breathing and clinically patent bilateral nasal airways. This case highlights delayed recognition of asymmetric bilateral congenital choanal obstruction and the practical diagnostic and operative adaptations required in a resource-limited setting. The outcome should be interpreted as favorable in the short term because objective postoperative endoscopic confirmation and long-term follow-up were not available.