This article reports a case of congenital choanal atresia with additional nostril and nasal deformities admitted to Henan Children's Hospital. A 43-day-old female patient was admitted to the hospital because of wheezing with mouth opening breathing and restricted feeding after birth'. The patient was diagnosis as bilateral congenital posterior nostril membranous atresia, congenital extra nostril nasal deformity and nasal stenosis by fiberoptic nasopharyngoscopy, CT, gene detection, and physical examination results. Under general anesthesia, endoscopic bilateral posterior nostril plasty and left anterior nostril plasty were performed. The child recovered well after operation.
摘要: 本文报道河南省儿童医院收治的1例先天性后鼻孔闭锁并额外鼻孔鼻腔畸形患儿。女，43 d，因“生后喘憋伴张口呼吸、吃奶受限”为代主诉入院，入院后完善纤维鼻咽镜、CT、基因检测并结合体检结果，诊断为：双侧先天性后鼻孔膜性闭锁、先天性额外鼻孔鼻腔畸形、鼻腔狭窄，于全身麻醉下行鼻内镜下双侧后鼻孔成形术及左侧前鼻孔成形术。术后患儿术后恢复良好。.
Keywords: congenital nature; nasal deformity; posterior nostril atresia; ventilation tube.
Copyright© by the Editorial Department of Journal of Clinical Otorhinolaryngology Head and Neck Surgery.