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成人双侧后鼻孔闭锁:能否存活?

Bilateral choanal atresia in an adult: is it compatible with life?

作者信息

Panda Naresh K, Simhadri Sridhar, Ghosh Shakuntala

机构信息

Department of Otolaryngology and Head and Neck Surgery, Postgraduate Institute of Medical Education and Research Chandigarh, India.

出版信息

J Laryngol Otol. 2004 Mar;118(3):244-5. doi: 10.1258/002221504322928099.

Abstract

Bilateral choanal atresia is potentially life-threatening. The condition almost always presents in the new born, with alternating phases of respiratory distress and apnoea relieved by crying. We report a rare case of bilateral choanal atresia presenting for the first time at 22 years of age. The patient had no features of cyanosis or apnoea, presenting only with bilateral nasal obstruction, rhinorrhoea and anosmia. His neonatal history was unremarkable. No syndromic association was noted excepting for telecanthus. The presence of bony atresia was confirmed on computed tomography (CT) scan and transnasal endoscopic surgery was used to obtain a patent airway. This case is a rare report of bilateral choanal atresia presenting for the first time in adult life.

摘要

双侧后鼻孔闭锁可能危及生命。这种情况几乎总是在新生儿期出现,表现为呼吸窘迫和呼吸暂停交替发作,哭闹时可缓解。我们报告一例罕见的双侧后鼻孔闭锁病例,患者22岁时首次出现症状。该患者无发绀或呼吸暂停症状,仅表现为双侧鼻塞、流涕和嗅觉丧失。其新生儿期病史无异常。除了内眦距增宽外,未发现综合征相关性。计算机断层扫描(CT)证实存在骨性闭锁,经鼻内镜手术建立了通畅的气道。该病例是双侧后鼻孔闭锁在成年期首次出现的罕见报道。

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