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引用本文的文献

1
, ., .
Indian J Otolaryngol Head Neck Surg. 2025 Jan;77(1):510-520. doi: 10.1007/s12070-024-05154-0. Epub 2024 Nov 20.

本文引用的文献

1
Congenital bony nasal cavity stenosis: A review of current trends in diagnosis and treatment.先天性骨性鼻腔狭窄：诊断与治疗现状的综述。
Int J Pediatr Otorhinolaryngol. 2021 May;144:110670. doi: 10.1016/j.ijporl.2021.110670. Epub 2021 Mar 6.
2
Congenital nasal pyriform aperture stenosis: a rare cause of neonatal nasal airway obstruction.先天性鼻梨状孔狭窄：新生儿鼻气道阻塞的罕见原因。
BJR Case Rep. 2015 Apr 20;1(1):20150006. doi: 10.1259/bjrcr.20150006. eCollection 2015.
3
Congenital nasal pyriform aperture stenosis 5.7 mm or less is associated with surgical intervention: A pooled case series.先天性鼻梨状孔狭窄5.7毫米及以下与手术干预相关：一项汇总病例系列研究。
Int J Pediatr Otorhinolaryngol. 2015 Nov;79(11):1802-5. doi: 10.1016/j.ijporl.2015.07.026. Epub 2015 Jul 28.
4
Congenital nasal pyriform aperture stenosis: diagnosis and management.先天性梨状孔狭窄：诊断与治疗。
Ital J Pediatr. 2012 Jun 26;38:28. doi: 10.1186/1824-7288-38-28.
5
Congenital nasal pyriform aperture stenosis: first case report in oman.先天性鼻梨状孔狭窄：阿曼首例病例报告。
Oman Med J. 2008 Jul;23(3):192-4.
6
Congenital nasal pyriform aperture stenosis: A rare cause of nasal airway obstruction in a neonate.先天性鼻梨状孔狭窄：新生儿鼻气道阻塞的罕见原因。
Indian J Radiol Imaging. 2010 Nov;20(4):266-8. doi: 10.4103/0971-3026.73539.
7
Congenital midnasal stenosis in an infant.一名婴儿的先天性中鼻狭窄。
Int J Pediatr Otorhinolaryngol. 2004 Jun;68(6):823-5. doi: 10.1016/j.ijporl.2004.01.008.
8
Midface anomalies in children.儿童面中部异常
Radiographics. 2000 Jul-Aug;20(4):907-22; quiz 1106-7, 1112. doi: 10.1148/radiographics.20.4.g00jl07907.
9
CT features of congenital nasal piriform aperture stenosis: initial experience.先天性鼻梨状孔狭窄的CT特征：初步经验
Radiology. 1999 Nov;213(2):495-501. doi: 10.1148/radiology.213.2.r99oc38495.

先天性鼻梨状孔狭窄

Congenital Nasal Pyriform Aperture Stenosis.

作者信息

Gandhi Sachin, Saindani Shradha, Mundalik Renuka

机构信息

Deenanath Mangeshkar Hospital, Pune, India.

出版信息

Indian J Otolaryngol Head Neck Surg. 2023 Dec;75(4):3953-3955. doi: 10.1007/s12070-023-03983-z. Epub 2023 Jun 22.

DOI:10.1007/s12070-023-03983-z
PMID:37974767
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10645990/
Abstract

Congenital nasal pyriform aperture stenosis (CNPAS) is a rare cause of neonatal stridor and airway obstruction. In this case report we present management of congenital CNPAS in an eight day old female child. Inability to pass nasogastric tube (of size 5Fr) raised suspicion of choanal atresia or pyriform aperture (PA) stenosis (PAS). Computed tomography scan of the paranasal sinuses is the investigation of choice. Transnasal endoscopic dilatation and stenting with ngt of 8Fr under general anaesthesia was done. In this case report we discuss the aetiology, presenting symptoms, diagnostic methods and treatment modalities for CNPAS.

摘要

先天性鼻梨状孔狭窄（CNPAS）是新生儿喘鸣和气道阻塞的罕见原因。在本病例报告中，我们介绍了一名8天大女婴先天性CNPAS的治疗情况。无法插入鼻胃管（5Fr）引发了对后鼻孔闭锁或梨状孔（PA）狭窄（PAS）的怀疑。鼻窦计算机断层扫描是首选的检查方法。在全身麻醉下进行了经鼻内镜扩张并用8Fr鼻胃管置入支架。在本病例报告中，我们讨论了CNPAS的病因、症状表现、诊断方法和治疗方式。