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先天性鼻梨状孔(骨性入口)狭窄

Congenital nasal pyriform aperture (bony inlet) stenosis.

作者信息

Ramadan H, Ortiz O

机构信息

Department of Otolaryngology-Head and Neck Surgery, West Virginia University, Morgantown 26506-9200, USA.

出版信息

Otolaryngol Head Neck Surg. 1995 Sep;113(3):286-9. doi: 10.1016/S0194-5998(95)70120-6.

Abstract

Congenital nasal pyriform aperture stenosis should be considered in the differential diagnosis of infants with nasal airway obstruction. It can occur as an isolated anomaly or it can be associated with other congenital anomalies. A history of cyclical respiratory distress and cyanosis often associated with feeding and relieved by crying is characteristic. On examination, the nasal airway is narrowed anteriorly. CT is the study of choice to make the diagnosis and rule out other causes of nasal obstruction. Conservative management is recommended, sometimes with the use of a McGovern nipple for feeding. Severe cases or those in which conservative management fails should be considered for surgery.

摘要

先天性鼻梨状孔狭窄应在婴儿鼻气道阻塞的鉴别诊断中予以考虑。它可作为一种孤立的异常情况出现,也可与其他先天性异常相关。常伴有喂养相关的周期性呼吸窘迫和发绀,哭闹后缓解的病史具有特征性。检查时,鼻气道前部变窄。CT是用于诊断和排除其他鼻阻塞原因的首选检查方法。建议采用保守治疗,有时可使用麦戈文奶嘴进行喂养。对于严重病例或保守治疗失败的病例,应考虑手术治疗。

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