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1
Congenital Laryngeal Stenosis and Concomitant Birth Defects in a Term Newborn: A Case Report.足月儿先天性喉狭窄及合并出生缺陷：一例报告
Biomed Hub. 2020 Jul 13;5(2):453-459. doi: 10.1159/000508731. eCollection 2020 May-Aug.
2
[Incidence of congenital heart defects in the Czech Republic--current data].[捷克共和国先天性心脏缺陷的发病率——当前数据]
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[Rate of prenatal detection of congenital right heart defects].[先天性右心缺陷的产前检测率]
Z Geburtshilfe Neonatol. 1999 Sep-Oct;203(5):207-12.
4
Cardiovascular malformations among preterm infants.早产儿中的心血管畸形。
Pediatrics. 2005 Dec;116(6):e833-8. doi: 10.1542/peds.2005-0397.
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Effect of Concomitant Birth Defects and Genetic Anomalies on Infant Mortality in Tetralogy of Fallot.法洛四联症并发出生缺陷和遗传异常对婴儿死亡率的影响。
Birth Defects Res. 2017 Aug 15;109(14):1154-1165. doi: 10.1002/bdr2.1057. Epub 2017 Jun 19.
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Successful simultaneous correction of complex congenital tracheal stenosis and tetralogy of fallot.成功同时矫正复杂先天性气管狭窄和法洛四联症。
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A rare congenital cardiac anomaly in adulthood: tetralogy of Fallot with absent pulmonary valve syndrome.成人罕见的先天性心脏异常：法洛四联症合并肺动脉瓣缺如综合征。
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本文引用的文献

1
Congenital respiratory tract disorders in 22q11.2 deletion syndrome.22q11.2缺失综合征中的先天性呼吸道疾病。
Int J Pediatr Otorhinolaryngol. 2018 Jan;104:1-4. doi: 10.1016/j.ijporl.2017.10.028. Epub 2017 Oct 20.
2
Association of airway abnormalities with 22q11.2 deletion syndrome.气道异常与22q11.2缺失综合征的关联。
Int J Pediatr Otorhinolaryngol. 2017 May;96:11-14. doi: 10.1016/j.ijporl.2017.02.012. Epub 2017 Feb 21.
3
Severe laryngeal stenosis in newly born twins with 22q11.2 deletion syndrome: A case report.患有22q11.2缺失综合征的新生儿双胞胎中的严重喉狭窄：一例报告。
J Neonatal Perinatal Med. 2016 May 18;9(2):223-6. doi: 10.3233/NPM-16915068.
4
Optimal Management of a 2-Hour-Old Newborn With Severe Congenital Subglottic Stenosis and Multiple Congenital Heart Diseases.患有严重先天性声门下狭窄和多种先天性心脏病的2小时大新生儿的最佳管理
Ann Otol Rhinol Laryngol. 2015 Dec;124(12):1006-10. doi: 10.1177/0003489415595422. Epub 2015 Jul 19.
5
Neonatal respiratory distress: a practical approach to its diagnosis and management.新生儿呼吸窘迫：其诊断与管理的实用方法
Pediatr Clin North Am. 2015 Apr;62(2):453-69. doi: 10.1016/j.pcl.2014.11.008.
6
Management specificities of congenital laryngeal stenosis: external and endoscopic approaches.先天性喉狭窄的治疗特点：外部和内镜方法。
Laryngoscope. 2014 Apr;124(4):1013-8. doi: 10.1002/lary.24373. Epub 2013 Oct 5.
7
Congenital and acquired developmental problems of the upper airway in newborns and infants.新生儿和婴儿上呼吸道的先天性和后天性发育问题。
Early Hum Dev. 2012 Dec;88(12):951-5. doi: 10.1016/j.earlhumdev.2012.09.001. Epub 2012 Sep 25.
8
Congenital anomalies of the larynx.喉先天性异常
Otolaryngol Clin North Am. 2007 Feb;40(1):177-91, viii. doi: 10.1016/j.otc.2006.10.004.
9
The upper airway: congenital malformations.上呼吸道：先天性畸形
Paediatr Respir Rev. 2006;7 Suppl 1:S260-3. doi: 10.1016/j.prrv.2006.04.227. Epub 2006 Jun 6.
10
Congenital laryngeal anomalies. Laryngeal atresia, stenosis, webs, and clefts.先天性喉异常。喉闭锁、狭窄、蹼和裂。
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足月儿先天性喉狭窄及合并出生缺陷：一例报告

Congenital Laryngeal Stenosis and Concomitant Birth Defects in a Term Newborn: A Case Report.

作者信息

Tesmer Patrycja, Wróblewska-Seniuk Katarzyna, Mazela Jan, Szydłowski Jarosław

机构信息

Department of Newborns' Infectious Diseases, Poznan University of Medical Sciences, Poznan, Poland.

Department of Otolaryngology, Head and Neck Surgery and Laryngological Oncology, Poznan University of Medical Sciences, Poznan, Poland.

出版信息

Biomed Hub. 2020 Jul 13;5(2):453-459. doi: 10.1159/000508731. eCollection 2020 May-Aug.

DOI:10.1159/000508731
PMID:32884930
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7443673/
Abstract

Congenital laryngeal stenosis is a rare and unusual anomaly that usually presents in the first minutes after delivery as severe life-threatening respiratory distress. It may exist as an isolated entity or in association with other congenital malformations, in particular cardiac anomalies. In this paper, we present the case of an infant with prenatal suspicion of tetralogy of Fallot. Immediately after delivery, the patient required intubation, which proved difficult. He was eventually diagnosed with laryngeal stenosis requiring laryngological treatment.

摘要

先天性喉狭窄是一种罕见且异常的畸形，通常在出生后的头几分钟内表现为严重的危及生命的呼吸窘迫。它可能作为一种孤立的病症存在，也可能与其他先天性畸形相关，尤其是心脏畸形。在本文中，我们介绍了一名产前怀疑患有法洛四联症的婴儿病例。出生后，该患者立即需要插管，但插管过程困难。他最终被诊断为喉狭窄，需要进行喉科治疗。