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青少年先天性H型气管食管瘘的神秘迟发表现——团队合作与手术规划

Mysterious Late Presentation of Congenital H-type Tracheoesophageal Fistula in Teenage - Teamwork and Operative Planning.

作者信息

Kotcharlakota Venkata Vijay, Shoor Gunjan, Singh Vishal, Kumar Ritesh, Joseph Keziah

机构信息

Depatrment of Cardiothoracic and Vascular Surgery, Mamata Academy of Medical Sciences, Bachupally, Hyderabad, Telangana, India.

Depatrment of Paediatric Surgery, Mamata Academy of Medical Sciences, Bachupally, Hyderabad, Telangana, India.

出版信息

J Indian Assoc Pediatr Surg. 2023 Jul-Aug;28(4):336-338. doi: 10.4103/jiaps.jiaps_63_23. Epub 2023 Jul 11.

DOI:10.4103/jiaps.jiaps_63_23
PMID:37635888
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10455701/
Abstract

Congenital tracheoesophageal fistula (TEF) is a result of the failed fusion of tracheoesophageal ridges during the 3 week of gestation. Commonly, TEF is associated with esophageal atresia, which is detected and treated in newborns. Isolated TEF is rare with an overall incidence of 1 in 80,000 live births. Very rarely, they can present in adulthood. This report is adding one such patient at the age of 17 years who presented with the first episode of aspiration pneumonia and a history of retrosternal discomfort and regurgitation since childhood to the limited world experience.

摘要

先天性气管食管瘘(TEF)是妊娠第3周时气管食管嵴融合失败的结果。通常,TEF与食管闭锁相关,食管闭锁在新生儿中可被检测到并进行治疗。孤立性TEF很少见,活产儿中的总体发病率为1/80000。极少数情况下,它们可在成年期出现。本报告将一名17岁的此类患者纳入有限的全球经验中,该患者首次出现吸入性肺炎,并有自幼以来的胸骨后不适和反流病史。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e9a/10455701/6e294728872b/JIAPS-28-336-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e9a/10455701/904ec97f74ae/JIAPS-28-336-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e9a/10455701/6e294728872b/JIAPS-28-336-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e9a/10455701/904ec97f74ae/JIAPS-28-336-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e9a/10455701/6e294728872b/JIAPS-28-336-g002.jpg

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Mysterious Late Presentation of Congenital H-type Tracheoesophageal Fistula in Teenage - Teamwork and Operative Planning.青少年先天性H型气管食管瘘的神秘迟发表现——团队合作与手术规划
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本文引用的文献

1
H-type Tracheoesophageal Fistula: A Rare Cause of Cough and Dysphagia in Adults.H型气管食管瘘:成人咳嗽和吞咽困难的罕见病因。
ACG Case Rep J. 2020 Dec 8;7(12):e00492. doi: 10.14309/crj.0000000000000492. eCollection 2020 Dec.
2
Congenital H-type tracheoesophageal fistula in adults.成人先天性H型气管食管瘘
J Thorac Dis. 2018 Jun;10(Suppl 16):S1905-S1910. doi: 10.21037/jtd.2018.05.200.
3
Congenital H-type tracheoesophageal fistula: A multicenter review of outcomes in a rare disease.先天性H型气管食管瘘:一种罕见疾病结局的多中心综述
J Pediatr Surg. 2017 Nov;52(11):1711-1714. doi: 10.1016/j.jpedsurg.2017.05.002. Epub 2017 May 11.
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H-type tracheo-oesophageal fistula.H型气管食管瘘
Arch Dis Child Fetal Neonatal Ed. 2007 Jan;92(1):F40. doi: 10.1136/adc.2006.100222.
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Thoracoscopic repair of tracheoesophageal fistula in a septuagenarian.
Ann Thorac Surg. 2006 May;81(5):1899-901. doi: 10.1016/j.athoracsur.2005.05.073.