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[梨状孔狭窄所致先天性鼻阻塞。病例系列]

[Congenital nasal obstruction due to pyriform aperture stenosis. A case series].

作者信息

Cuestas G, José G, Demarchi V, Razetti J, Boccio C

机构信息

Servicio de Otorrinolaringología, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.

Servicio de Otorrinolaringología, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.

出版信息

An Pediatr (Barc). 2015 Jan;82(1):e44-7. doi: 10.1016/j.anpedi.2013.12.009. Epub 2014 Mar 11.

Abstract

Nasal obstruction in neonates is a potentially fatal condition due to their exclusive nasal breathing. The main cause is inflammatory or infectious rhinitis. Congenital, neoplastic, traumatic or iatrogenic causes are less frequent. Choanal atresia is the most common congenital nasal anomaly. A less common etiology of congenital nasal obstruction is pyriform aperture stenosis. Suspicion might arise in any newborn with varying degrees of stridor and respiratory distress, associated with the difficulty of passing a probe through anterior nares. Diagnosis should be confirmed by a computed tomography of the craniofacial massif. The therapeutic approach will depend on the severity of symptoms. We describe our experience with 5 patients with this condition, treated surgically using a sub-labial approach, and followed by nasal stenting.

摘要

由于新生儿仅通过鼻腔呼吸,鼻阻塞是一种潜在的致命病症。主要病因是炎性或感染性鼻炎。先天性、肿瘤性、创伤性或医源性病因则较少见。后鼻孔闭锁是最常见的先天性鼻异常。先天性鼻阻塞的一种较罕见病因是梨状孔狭窄。任何出现不同程度喘鸣和呼吸窘迫、伴有经前鼻孔插入探针困难的新生儿都可能引起怀疑。诊断应通过颅面部断层扫描来确认。治疗方法将取决于症状的严重程度。我们描述了5例该病症患者的治疗经验,采用唇下入路进行手术治疗,并随后进行鼻腔支架置入。

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