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BMJ Case Rep. 2021 May 7;14(5):e240149. doi: 10.1136/bcr-2020-240149.
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Congenital nasal pyriform aperture stenosis.先天性鼻梨状孔狭窄
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7
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Congenital nasal pyriform aperture stenosis: clinical and radiologic findings and treatment.先天性鼻前孔狭窄:临床和影像学表现及治疗。
Jpn J Radiol. 2009 Nov;27(9):389-91. doi: 10.1007/s11604-009-0354-z. Epub 2009 Nov 27.
9
Computational fluid dynamics (CFD), virtual rhinomanometry, and virtual surgery for neonatal congenital nasal pyriform aperture stenosis.新生儿先天性鼻梨状孔狭窄的计算流体动力学(CFD)、虚拟鼻测压法和虚拟手术
Int J Pediatr Otorhinolaryngol. 2024 Jul;182:112025. doi: 10.1016/j.ijporl.2024.112025. Epub 2024 Jun 28.
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Congenital nasal pyriform aperture stenosis: diagnosis and treatment.先天性鼻梨状孔狭窄:诊断与治疗
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引用本文的文献

1
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2
Use of an Orthodontic and Otolaryngological Approach in an Infant with Holoprosencephaly.在一名患全前脑畸形的婴儿中采用正畸和耳鼻喉科治疗方法。
Children (Basel). 2024 May 5;11(5):554. doi: 10.3390/children11050554.

本文引用的文献

1
Choanal Atresia and Other Neonatal Nasal Anomalies.后鼻孔闭锁及其他新生儿鼻腔异常。
Clin Perinatol. 2018 Dec;45(4):751-767. doi: 10.1016/j.clp.2018.07.011. Epub 2018 Sep 18.
2
Congenital nasal obstruction in infants: A retrospective study and literature review.婴儿先天性鼻阻塞:一项回顾性研究及文献综述
Int J Pediatr Otorhinolaryngol. 2017 Aug;99:78-84. doi: 10.1016/j.ijporl.2017.05.023. Epub 2017 May 30.
3
Pyriform aperture enlargement in all aspects.梨状孔各方面扩大。
J Laryngol Otol. 2017 Jun;131(6):476-479. doi: 10.1017/S0022215117000391. Epub 2017 Feb 27.
4
Congenital nasal pyriform aperture stenosis in association with solitary median maxillary central incisor: unique radiologic features.先天性鼻梨状孔狭窄合并上颌正中单颗中切牙:独特的影像学特征。
Radiol Case Rep. 2016 Aug 1;11(3):178-81. doi: 10.1016/j.radcr.2016.06.004. eCollection 2016 Sep.
5
Rarely Seen Nasal Congenital Problems Causing Neonatal Upper Respiratory Obstruction: A Case Series.导致新生儿上呼吸道梗阻的罕见鼻先天性问题:病例系列
Pediatr Rep. 2016 Mar 31;8(1):6456. doi: 10.4081/pr.2016.6456.
6
Congenital nasal pyriform aperture stenosis: Elaboration of a management algorithm from 25 years of experience.先天性鼻梨状孔狭窄:基于25年经验制定的治疗方案
Int J Pediatr Otorhinolaryngol. 2016 Apr;83:7-11. doi: 10.1016/j.ijporl.2016.01.011. Epub 2016 Jan 25.
7
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.
8
Novel treatment of neonates with congenital nasal pyriform aperture stenosis.
Laryngoscope. 2015 Dec;125(12):2816-9. doi: 10.1002/lary.25198. Epub 2015 Feb 13.
9
Patient selection in congenital pyriform aperture stenosis repair - 14 year experience and systematic review of literature.先天性梨状孔狭窄修复中的患者选择——14年经验及文献系统综述
Int J Pediatr Otorhinolaryngol. 2015 Feb;79(2):235-9. doi: 10.1016/j.ijporl.2014.12.016. Epub 2014 Dec 22.
10
Clinical course and implications of congenital nasal pyriform stenosis and solitary median maxillary central incisor in a newborn: a case report.新生儿先天性鼻梨状孔狭窄合并孤立性上颌中切牙的临床过程及影响:一例报告
J Med Case Rep. 2014 Jun 20;8:215. doi: 10.1186/1752-1947-8-215.

先天性鼻梨状孔狭窄的新型上颌骨扩大技术:一例报告及文献综述

Novel maxillary enlargement technique in congenital nasal pyriform aperture stenosis: a case report and literature review.

作者信息

Hallikainen Joona, Seppa Juha, Kellokoski Jari

机构信息

Oral and Maxillofacial Diaseases, Kuopio University Hospital, Kuopio, Finland

Head and Neck center, Kuopio University Hospital, Kuopio, Finland.

出版信息

BMJ Case Rep. 2021 May 7;14(5):e240149. doi: 10.1136/bcr-2020-240149.

DOI:10.1136/bcr-2020-240149
PMID:33962919
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8108663/
Abstract

Congenital nasal pyriform aperture stenosis (CNPAS) is a rare cause of neonate nasal obstruction. Because newborns are natural nasal breathers, urgent treatment may be needed. CNPAS is diagnosed by clinical symptoms and signs, and CT. In severe cases, surgical approach is needed. The most often used approach is widening of pyriform aperture via sublabial incision with nasal tubing. We report a novel surgical approach as a curative treatment for CNPAS by immediate transverse enlargement of the maxilla. We also review current literature of the condition focusing on surgical management of the disease.

摘要

先天性鼻梨状孔狭窄(CNPAS)是新生儿鼻塞的罕见原因。由于新生儿是自然的鼻呼吸者,可能需要紧急治疗。CNPAS通过临床症状、体征及CT进行诊断。在严重病例中,需要采取手术方法。最常用的方法是经唇下切口置入鼻管扩大梨状孔。我们报告一种通过立即横向扩大上颌骨来治疗CNPAS的新手术方法。我们还综述了关于该疾病状况的当前文献,重点关注其手术治疗。