Esophageal atresia with distal tracheoesophageal fistula with gasless abdomen: a diagnostic dilemma

10.5580/101d ◽  
2009 ◽  
Vol 9 (2) ◽  
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 ◽  
...  

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.


1980 ◽  
Vol 15 (6) ◽  
pp. 857-862 ◽  
Author(s):  
Stephen G. Jolley ◽  
Dale G. Johnson ◽  
Charles C. Roberts ◽  
John J. Herbst ◽  
Michael E. Matlak ◽  
...  

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