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Simultaneous duodenal stenosis and duodenal web in a newborn

Failure of duodenal recanalization results in a spectrum of proximal bowel obstruction from stenosis to atresia. Associations between congenital duodenal obstruction and other congenital anomalies have been well documented although the coincidence of duodenal stenosis and duodenal web is incredibly...

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Autores principales: Erickson, James, Retrouvey, Michele, Rush, Jennifer, Trace, Anthony P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5128381/
https://www.ncbi.nlm.nih.gov/pubmed/27920877
http://dx.doi.org/10.1016/j.radcr.2016.08.017
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author Erickson, James
Retrouvey, Michele
Rush, Jennifer
Trace, Anthony P.
author_facet Erickson, James
Retrouvey, Michele
Rush, Jennifer
Trace, Anthony P.
author_sort Erickson, James
collection PubMed
description Failure of duodenal recanalization results in a spectrum of proximal bowel obstruction from stenosis to atresia. Associations between congenital duodenal obstruction and other congenital anomalies have been well documented although the coincidence of duodenal stenosis and duodenal web is incredibly rare, posing a unique diagnostic challenge. We report a case of a full-term 4-day-old female child presented with forceful, bilious emesis and poor oral intake with decreased frequency of urination, and stooling whose initial abdominal radiograph showed several loops of gas-filled bowel in the distal stomach and proximal duodenum mimicking the classic “double-bubble” sign. An upper gastrointestinal barium contrast study revealed distention of the duodenal bulb with an abrupt narrowing and subsequent dilation at the second portion of the duodenum raising the suggestion of multiple duodenal obstructions. Ladd’s procedure was performed, and the stenotic and webbed segments were bypassed with a Kimura diamond-shaped duodenoduodenostomy.
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spelling pubmed-51283812016-12-05 Simultaneous duodenal stenosis and duodenal web in a newborn Erickson, James Retrouvey, Michele Rush, Jennifer Trace, Anthony P. Radiol Case Rep Case Report Failure of duodenal recanalization results in a spectrum of proximal bowel obstruction from stenosis to atresia. Associations between congenital duodenal obstruction and other congenital anomalies have been well documented although the coincidence of duodenal stenosis and duodenal web is incredibly rare, posing a unique diagnostic challenge. We report a case of a full-term 4-day-old female child presented with forceful, bilious emesis and poor oral intake with decreased frequency of urination, and stooling whose initial abdominal radiograph showed several loops of gas-filled bowel in the distal stomach and proximal duodenum mimicking the classic “double-bubble” sign. An upper gastrointestinal barium contrast study revealed distention of the duodenal bulb with an abrupt narrowing and subsequent dilation at the second portion of the duodenum raising the suggestion of multiple duodenal obstructions. Ladd’s procedure was performed, and the stenotic and webbed segments were bypassed with a Kimura diamond-shaped duodenoduodenostomy. Elsevier 2016-10-01 /pmc/articles/PMC5128381/ /pubmed/27920877 http://dx.doi.org/10.1016/j.radcr.2016.08.017 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Erickson, James
Retrouvey, Michele
Rush, Jennifer
Trace, Anthony P.
Simultaneous duodenal stenosis and duodenal web in a newborn
title Simultaneous duodenal stenosis and duodenal web in a newborn
title_full Simultaneous duodenal stenosis and duodenal web in a newborn
title_fullStr Simultaneous duodenal stenosis and duodenal web in a newborn
title_full_unstemmed Simultaneous duodenal stenosis and duodenal web in a newborn
title_short Simultaneous duodenal stenosis and duodenal web in a newborn
title_sort simultaneous duodenal stenosis and duodenal web in a newborn
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5128381/
https://www.ncbi.nlm.nih.gov/pubmed/27920877
http://dx.doi.org/10.1016/j.radcr.2016.08.017
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