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Clinico-Radiological Diagnosis of Isolated Congenital Esophageal Stenosis in a Preterm Neonate

A 2-day-old preterm female neonate weighing 1.6 kg and having excessive frothing from mouth was investigated for suspected esophageal atresia and tracheoesophageal fistula. X-ray findings of an unusually low-ending upper pouch (up to T(8) level) and the absence of gas in abdomen lead to suspicion of...

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Autor principal: Sham, Minakshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Georg Thieme Verlag KG 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4336058/
https://www.ncbi.nlm.nih.gov/pubmed/25755945
http://dx.doi.org/10.1055/s-0033-1345279
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author Sham, Minakshi
author_facet Sham, Minakshi
author_sort Sham, Minakshi
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description A 2-day-old preterm female neonate weighing 1.6 kg and having excessive frothing from mouth was investigated for suspected esophageal atresia and tracheoesophageal fistula. X-ray findings of an unusually low-ending upper pouch (up to T(8) level) and the absence of gas in abdomen lead to suspicion of an unusual variety of esophageal atresia. Hence unlike the usual management of pure esophageal atresia, in terms of esophagostomy and gastrostomy in neonatal period, right thoracotomy was performed allowing successful primary anastomosis. A high index of suspicion on the basis of radiological picture led to early diagnosis of a rare anomaly like congenital esophageal stenosis and successful management of this low birth weight baby.
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spelling pubmed-43360582015-03-09 Clinico-Radiological Diagnosis of Isolated Congenital Esophageal Stenosis in a Preterm Neonate Sham, Minakshi European J Pediatr Surg Rep Article A 2-day-old preterm female neonate weighing 1.6 kg and having excessive frothing from mouth was investigated for suspected esophageal atresia and tracheoesophageal fistula. X-ray findings of an unusually low-ending upper pouch (up to T(8) level) and the absence of gas in abdomen lead to suspicion of an unusual variety of esophageal atresia. Hence unlike the usual management of pure esophageal atresia, in terms of esophagostomy and gastrostomy in neonatal period, right thoracotomy was performed allowing successful primary anastomosis. A high index of suspicion on the basis of radiological picture led to early diagnosis of a rare anomaly like congenital esophageal stenosis and successful management of this low birth weight baby. Georg Thieme Verlag KG 2013-05-16 2013-06 /pmc/articles/PMC4336058/ /pubmed/25755945 http://dx.doi.org/10.1055/s-0033-1345279 Text en © Thieme Medical Publishers
spellingShingle Article
Sham, Minakshi
Clinico-Radiological Diagnosis of Isolated Congenital Esophageal Stenosis in a Preterm Neonate
title Clinico-Radiological Diagnosis of Isolated Congenital Esophageal Stenosis in a Preterm Neonate
title_full Clinico-Radiological Diagnosis of Isolated Congenital Esophageal Stenosis in a Preterm Neonate
title_fullStr Clinico-Radiological Diagnosis of Isolated Congenital Esophageal Stenosis in a Preterm Neonate
title_full_unstemmed Clinico-Radiological Diagnosis of Isolated Congenital Esophageal Stenosis in a Preterm Neonate
title_short Clinico-Radiological Diagnosis of Isolated Congenital Esophageal Stenosis in a Preterm Neonate
title_sort clinico-radiological diagnosis of isolated congenital esophageal stenosis in a preterm neonate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4336058/
https://www.ncbi.nlm.nih.gov/pubmed/25755945
http://dx.doi.org/10.1055/s-0033-1345279
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