scholarly journals Preterm Infant with Congenital Tracheal Diverticulum in the Presence of Esophageal Atresia and Tracheoesophageal Fistula

2018 ◽  
Vol 7 (4) ◽  
pp. 44
Author(s):  
Alessandra Glover Williams ◽  
Janet McNally ◽  
Julian Gaskin ◽  
Ela Chakkarapani

A 32+4-week-preterm neonate was operated on day 1 for esophageal atresia with tracheoesophageal fistula with a tight primary anastomosis and closure of a tracheoesophageal fistula. Postoperatively, he needed ventilation for 6 days. Post-extubation, he needed continuous positive airway pressure support for increased work of breathing, increasing oxygen requirement, and respiratory acidosis when respiratory support was weaned. Further, during the post-operative period, he had right hemidiaphragmatic paresis and acute lifethreatening events requiring manual high-pressure, non-invasive positive pressure ventilation resuscitation. These complications were considered, and a computed tomography assisted by three-dimensional reconstruction was performed. This revealed a congenital tracheal diverticulum and severe tracheomalacia which was confirmed with microlaryngoscopy and bronchoscopy. The presentation and the diagnostic dilemma surrounding this rare diagnosis are discussed in this case report.

2014 ◽  
Vol 34 (1) ◽  
pp. 71-73
Author(s):  
S Adhikari ◽  
K Malla ◽  
P Poudyal

Tracheoesophageal fistula (TEF) without associated esophageal atresia (EA) is a rare congenital anomaly.  Most of the children are treated for episodes of pneumonia prior to definitive diagnosis.  A 5 months infant presented with recurrent pneumonia and diagnosis of H type TEF was made with contrast esophagram.DOI: http://dx.doi.org/10.3126/jnps.v34i1.8517   J Nepal Paediatr Soc 2014;34(1):71-73


2018 ◽  
Vol 7 (2) ◽  
pp. 23
Author(s):  
Shailesh Solanki ◽  
Ravi Prakash Kanojia ◽  
Ram Samujh

Esophageal atresia with tracheoesophageal fistula (EA-TEF) is a well-known congenital anomaly and Type C variety of gross classification is the most common. Even for Type C variety, anatomy of upper pouch and lower pouch is not always the same. We are presenting three cases of Type C EA-TEF with unusual anatomy. In this type, upper pouch crosses over the lower pouch for a significant length. The cases are described here to highlight this variant of Type C EA-TEF which produces diagnostic dilemma. An early diagnosis of this variant, prevents morbidity and mortality.


1997 ◽  
Vol 12 (2-3) ◽  
pp. 186-187
Author(s):  
A. N. Gangopadhyay ◽  
S. P. Sahoo ◽  
C. K. Sinha ◽  
S. Chooramani Gopal ◽  
D. K. Gupta ◽  
...  

1997 ◽  
Vol 12 (2-3) ◽  
pp. 186-187 ◽  
Author(s):  
C. K. Sinha ◽  
A. N. Gangopadhyay ◽  
S. P. Sahoo ◽  
S. Chooramani Gopal ◽  
D. K. Gupta ◽  
...  

2019 ◽  
Vol 30 (06) ◽  
pp. 475-482 ◽  
Author(s):  
Carmen Dingemann ◽  
Simon Eaton ◽  
Gunnar Aksnes ◽  
Pietro Bagolan ◽  
Kate M. Cross ◽  
...  

Abstract Introduction Improvements in care of patients with esophageal atresia (EA) and tracheoesophageal fistula (TEF) have shifted the focus from mortality to morbidity and quality-of-life. Long-term follow-up is essential, but evidence is limited and standardized protocols are scarce. Nineteen representatives of the European Reference Network for Rare Inherited Congenital Anomalies (ERNICA) from nine European countries conducted a consensus conference on the surgical management of EA/TEF. Materials and Methods The conference was prepared by item generation (including items of surgical relevance from the European Society for Pediatric Gastroenterology Hepatology and Nutrition (ESPGHAN)-The North American Society for Pediatric Gastroenterology, Hepatology and Nutrition (NASPGHAN) guidelines on follow-up after EA repair), item prioritization, formulation of a final list containing the domains Follow-up and Framework, and literature review. Anonymous voting was conducted via an internet-based system. Consensus was defined as ≥75% of those voting with scores of 6 to 9. Results Twenty-five items were generated in the domain Follow-up of which 17 (68%) matched with corresponding ESPGHAN-NASPGHAN statements. Complete consensus (100%) was achieved on seven items (28%), such as the necessity of an interdisciplinary follow-up program. Consensus ≥75% was achieved on 18 items (72%), such as potential indications for fundoplication. There was an 82% concordance with the ESPGHAN-NASPGHAN recommendations. Four items were generated in the domain Framework, and complete consensus was achieved on all these items. Conclusion Participants of the first ERNICA conference reached significant consensus on the follow-up of patients with EA/TEF who undergo primary anastomosis. Fundamental statements regarding centralization, multidisciplinary approach, and involvement of patient organizations were formulated. These consensus statements will provide the cornerstone for uniform treatment protocols and resultant optimized patient care.


2000 ◽  
Vol 175 (5) ◽  
pp. 1403-1407 ◽  
Author(s):  
Suat Fitoz ◽  
Çetin Atasoy ◽  
Aydin Yagmurlu ◽  
Serdar Akyar ◽  
Ayşe Erden ◽  
...  

2019 ◽  
Vol 39 (3) ◽  
pp. 253-256
Author(s):  
Akihiro YAMADA ◽  
Tomoko OKUMURA ◽  
Noriyuki MORIMOTO ◽  
Kazuko HASEGAWA ◽  
Yoko ARAKAWA ◽  
...  

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