Congenital short bowel syndrome: a rare cause of neonatal intestinal obstruction

Congenital short bowel syndrome (CSBS) is an uncommon gastrointestinal disorder in which an unclear aetiology causes considerable intrauterine reduction in small bowel length. As a result of reduced absorptive intestinal length, chronic diarrhoea, vomiting, and consequently, failure to thrive are li...

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Detalles Bibliográficos
Autores principales: Zain, Mostafa, Abdelkader, Mansour, Azab, Ahmed, Kotb, Mostafa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7509730/
https://www.ncbi.nlm.nih.gov/pubmed/32951488
http://dx.doi.org/10.1177/0300060520954726
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author Zain, Mostafa
Abdelkader, Mansour
Azab, Ahmed
Kotb, Mostafa
author_facet Zain, Mostafa
Abdelkader, Mansour
Azab, Ahmed
Kotb, Mostafa
author_sort Zain, Mostafa
collection PubMed
description Congenital short bowel syndrome (CSBS) is an uncommon gastrointestinal disorder in which an unclear aetiology causes considerable intrauterine reduction in small bowel length. As a result of reduced absorptive intestinal length, chronic diarrhoea, vomiting, and consequently, failure to thrive are likely. We report a case of CSBS in a 26-day-old girl who had malrotation and a short bowel with a length of bowel from the pylorus to the ileocecal junction of approximately 40 cm. The patient underwent Ladd’s procedure, but she is still dependent on parenteral nutrition.
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spelling pubmed-75097302020-10-01 Congenital short bowel syndrome: a rare cause of neonatal intestinal obstruction Zain, Mostafa Abdelkader, Mansour Azab, Ahmed Kotb, Mostafa J Int Med Res Case Report Congenital short bowel syndrome (CSBS) is an uncommon gastrointestinal disorder in which an unclear aetiology causes considerable intrauterine reduction in small bowel length. As a result of reduced absorptive intestinal length, chronic diarrhoea, vomiting, and consequently, failure to thrive are likely. We report a case of CSBS in a 26-day-old girl who had malrotation and a short bowel with a length of bowel from the pylorus to the ileocecal junction of approximately 40 cm. The patient underwent Ladd’s procedure, but she is still dependent on parenteral nutrition. SAGE Publications 2020-09-21 /pmc/articles/PMC7509730/ /pubmed/32951488 http://dx.doi.org/10.1177/0300060520954726 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Zain, Mostafa
Abdelkader, Mansour
Azab, Ahmed
Kotb, Mostafa
Congenital short bowel syndrome: a rare cause of neonatal intestinal obstruction
title Congenital short bowel syndrome: a rare cause of neonatal intestinal obstruction
title_full Congenital short bowel syndrome: a rare cause of neonatal intestinal obstruction
title_fullStr Congenital short bowel syndrome: a rare cause of neonatal intestinal obstruction
title_full_unstemmed Congenital short bowel syndrome: a rare cause of neonatal intestinal obstruction
title_short Congenital short bowel syndrome: a rare cause of neonatal intestinal obstruction
title_sort congenital short bowel syndrome: a rare cause of neonatal intestinal obstruction
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7509730/
https://www.ncbi.nlm.nih.gov/pubmed/32951488
http://dx.doi.org/10.1177/0300060520954726
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