Double H-type tracheoesophageal fistula

Congenital ‘isolated’ tracheoesophageal fistula (TEF) is a rare variant of esophageal atresia, also termed H-type TEF. Even rarer is a double H-type TEF. Here, we report a two-week-old female, with double H-type TEF – one identified pre-operatively, the other during surgery. Pre-operative laryngotra...

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Main Authors: Sharman P. Tan Tanny, Sebastian K. King, Taher I. Omari, Warwick J. Teague
Format: Article
Language:English
Published: Elsevier 2020-11-01
Series:Journal of Pediatric Surgery Case Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2213576620302967
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spelling doaj-b39e6ea2ce064684a67c1583f11cca0e2020-11-25T03:37:06ZengElsevierJournal of Pediatric Surgery Case Reports2213-57662020-11-0162101662Double H-type tracheoesophageal fistulaSharman P. Tan Tanny0Sebastian K. King1Taher I. Omari2Warwick J. Teague3Department of Paediatric Surgery, The Royal Children's Hospital, 50 Flemington Road, Parkville, VIC, 3052, Australia; F. Douglas Stephens Surgical Research Group, Murdoch Children's Research Institute, 50 Flemington Road, Parkville, VIC, 3052, Australia; Department of Paediatrics, University of Melbourne, Parkville, VIC, 3052, AustraliaDepartment of Paediatric Surgery, The Royal Children's Hospital, 50 Flemington Road, Parkville, VIC, 3052, Australia; F. Douglas Stephens Surgical Research Group, Murdoch Children's Research Institute, 50 Flemington Road, Parkville, VIC, 3052, Australia; Department of Paediatrics, University of Melbourne, Parkville, VIC, 3052, AustraliaDepartment of Human Physiology, Flinders University, Sturt Road, Bedford Park, SA, 5042, AustraliaDepartment of Paediatric Surgery, The Royal Children's Hospital, 50 Flemington Road, Parkville, VIC, 3052, Australia; F. Douglas Stephens Surgical Research Group, Murdoch Children's Research Institute, 50 Flemington Road, Parkville, VIC, 3052, Australia; Department of Paediatrics, University of Melbourne, Parkville, VIC, 3052, Australia; Corresponding author. Department of Paediatric Surgery, The Royal Children's Hospital, 50 Flemington Road, Parkville, VIC, 3052, Australia.Congenital ‘isolated’ tracheoesophageal fistula (TEF) is a rare variant of esophageal atresia, also termed H-type TEF. Even rarer is a double H-type TEF. Here, we report a two-week-old female, with double H-type TEF – one identified pre-operatively, the other during surgery. Pre-operative laryngotracheobronchoscopy (LTB) with guidewire cannulation is considered key to definitive TEF repair, to aid in both pre- and intra-operative identification of the fistula(e). In our experience, only one H-type TEF was identified at the planned pre-operative LTB, with the second H-type fistula identified at the time of cervical dissection. Both fistulae were repaired during the same operation, via cervical approach. This represents the first reported case of a double H-type TEF, repaired primarily via a single cervical incision.http://www.sciencedirect.com/science/article/pii/S2213576620302967Tracheoesophageal fistulaCongenitalCase report
collection DOAJ
language English
format Article
sources DOAJ
author Sharman P. Tan Tanny
Sebastian K. King
Taher I. Omari
Warwick J. Teague
spellingShingle Sharman P. Tan Tanny
Sebastian K. King
Taher I. Omari
Warwick J. Teague
Double H-type tracheoesophageal fistula
Journal of Pediatric Surgery Case Reports
Tracheoesophageal fistula
Congenital
Case report
author_facet Sharman P. Tan Tanny
Sebastian K. King
Taher I. Omari
Warwick J. Teague
author_sort Sharman P. Tan Tanny
title Double H-type tracheoesophageal fistula
title_short Double H-type tracheoesophageal fistula
title_full Double H-type tracheoesophageal fistula
title_fullStr Double H-type tracheoesophageal fistula
title_full_unstemmed Double H-type tracheoesophageal fistula
title_sort double h-type tracheoesophageal fistula
publisher Elsevier
series Journal of Pediatric Surgery Case Reports
issn 2213-5766
publishDate 2020-11-01
description Congenital ‘isolated’ tracheoesophageal fistula (TEF) is a rare variant of esophageal atresia, also termed H-type TEF. Even rarer is a double H-type TEF. Here, we report a two-week-old female, with double H-type TEF – one identified pre-operatively, the other during surgery. Pre-operative laryngotracheobronchoscopy (LTB) with guidewire cannulation is considered key to definitive TEF repair, to aid in both pre- and intra-operative identification of the fistula(e). In our experience, only one H-type TEF was identified at the planned pre-operative LTB, with the second H-type fistula identified at the time of cervical dissection. Both fistulae were repaired during the same operation, via cervical approach. This represents the first reported case of a double H-type TEF, repaired primarily via a single cervical incision.
topic Tracheoesophageal fistula
Congenital
Case report
url http://www.sciencedirect.com/science/article/pii/S2213576620302967
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