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J Clin Diagn Res. 2014 Feb;8(2):171-2. doi: 10.7860/JCDR/2014/6582.4048. Epub 2014 Feb 3.
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Tracheal agenesis: approach towards this severe diagnosis. Case report and review of the literature.气管发育不全：对这一严重诊断的处理方法。病例报告和文献复习。
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本文引用的文献

1
Tracheal agenesis with broncho-esophageal fistula in VACTERL / TACRD association.VACTERL/TACRD综合征合并气管闭锁及支气管食管瘘
Indian J Hum Genet. 2013 Jan;19(1):87-9. doi: 10.4103/0971-6866.112910.
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Tracheal agenesis: A rare but fatal congenital anomaly.气管闭锁：一种罕见但致命的先天性异常。
Mcgill J Med. 2011 Jun;13(1):10.
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Tracheal agenesis: approach towards this severe diagnosis. Case report and review of the literature.气管发育不全：对这一严重诊断的处理方法。病例报告和文献复习。
Eur J Pediatr. 2012 Mar;171(3):425-31. doi: 10.1007/s00431-011-1563-x. Epub 2011 Sep 15.
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A long-term survival case of tracheal agenesis: management for tracheoesophageal fistula and esophageal reconstruction.一例气管闭锁长期存活病例：食管气管瘘的处理及食管重建
Pediatr Surg Int. 2011 Jan;27(1):103-6. doi: 10.1007/s00383-010-2716-0.
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Three-stage reconstruction of the airway and alimentary tract in a case of tracheal agenesis.气管发育不全病例的气道和消化道三阶段重建。
Ann Thorac Surg. 2010 Jun;89(6):2019-22. doi: 10.1016/j.athoracsur.2009.11.021.
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Management of tracheal agenesis.气管发育不全的管理
Paediatr Anaesth. 2000;10(4):441-4. doi: 10.1046/j.1460-9592.2000.00549.x.
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Congenital absence of the trachea.
Eur J Pediatr. 2000 Jan-Feb;159(1-2):8-13. doi: 10.1007/s004310050002.
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Tracheal agenesis in a child who survived for 6 years.
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Tracheal agenesis: a case report and review of the literature.气管发育不全：一例病例报告及文献综述
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气管闭锁伴气管食管瘘

Tracheal Agenesis with Tracheo-oesophageal Fistula.

作者信息

Nimbalkar Somashekhar Marutirao, Patel Vijay K, Patel Dipen Vasudev, Sethi Ankur Rajinder

机构信息

Professor, Department of Paediatrics, Pramukhswami Medical College , Karamsad, Gujarat, India .

Senior Resident, Department of Paediatrics, Pramukhswami Medical College , Karamsad, Gujarat, India .

出版信息

J Clin Diagn Res. 2014 Feb;8(2):171-2. doi: 10.7860/JCDR/2014/6582.4048. Epub 2014 Feb 3.

DOI:10.7860/JCDR/2014/6582.4048
PMID:24701523
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3972551/
Abstract

Tracheal Agenesis (TA) presents with respiratory distress at birth. Diagnosis requires recognition of clinical signs in newborns like failure of endotracheal intubation, respiratory distress with absent air entry over both side of chest and inaudible cry. We describe a TA Floyd Type I with a Tracheo-Oesophageal Fistula (TOF) without other congenital malformations.

摘要

气管闭锁（TA）在出生时即出现呼吸窘迫。诊断需要识别新生儿的临床体征，如气管插管失败、双侧胸廓呼吸音消失伴呼吸窘迫以及哭声听不到。我们描述了一例伴有气管食管瘘（TOF）的I型弗洛伊德气管闭锁，无其他先天性畸形。