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Jejunal Choristoma: A Very Rare Cause of Abdominal Pain in Children

Choristoma is development of a normal tissue in an aberrant location. This report describes jejunal salivary choristoma (JSC) causing recurring episodes of abdominal discomfort in a 5-year-old girl. Exploratory laporatomy revealed a pale yellow subserosal jejunal lesion. Wedge resection of the lesio...

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Autores principales: Olajide, T. A., Agodirin, S. O., Ojewola, R. W., Akanbi, O. O., Solaja, T. O., Odesanya, Johnson Oluremi, Ariyibi, O. O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3910446/
https://www.ncbi.nlm.nih.gov/pubmed/24511408
http://dx.doi.org/10.1155/2014/863647
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author Olajide, T. A.
Agodirin, S. O.
Ojewola, R. W.
Akanbi, O. O.
Solaja, T. O.
Odesanya, Johnson Oluremi
Ariyibi, O. O.
author_facet Olajide, T. A.
Agodirin, S. O.
Ojewola, R. W.
Akanbi, O. O.
Solaja, T. O.
Odesanya, Johnson Oluremi
Ariyibi, O. O.
author_sort Olajide, T. A.
collection PubMed
description Choristoma is development of a normal tissue in an aberrant location. This report describes jejunal salivary choristoma (JSC) causing recurring episodes of abdominal discomfort in a 5-year-old girl. Exploratory laporatomy revealed a pale yellow subserosal jejunal lesion. Wedge resection of the lesion and repair of the bowel were performed. The child did well postoperatively and has since that time been free of pain at follow-up. Histopathological examination of the resected lesion revealed salivary gland choriostoma. Literature review (PUBMED search engine) revealed no previous report of this rare clinicopathologic entity. We conclude that choriostoma should be considered a possible differential when evaluating abdominal complaint in children.
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spelling pubmed-39104462014-02-09 Jejunal Choristoma: A Very Rare Cause of Abdominal Pain in Children Olajide, T. A. Agodirin, S. O. Ojewola, R. W. Akanbi, O. O. Solaja, T. O. Odesanya, Johnson Oluremi Ariyibi, O. O. Case Rep Surg Case Report Choristoma is development of a normal tissue in an aberrant location. This report describes jejunal salivary choristoma (JSC) causing recurring episodes of abdominal discomfort in a 5-year-old girl. Exploratory laporatomy revealed a pale yellow subserosal jejunal lesion. Wedge resection of the lesion and repair of the bowel were performed. The child did well postoperatively and has since that time been free of pain at follow-up. Histopathological examination of the resected lesion revealed salivary gland choriostoma. Literature review (PUBMED search engine) revealed no previous report of this rare clinicopathologic entity. We conclude that choriostoma should be considered a possible differential when evaluating abdominal complaint in children. Hindawi Publishing Corporation 2014 2014-01-08 /pmc/articles/PMC3910446/ /pubmed/24511408 http://dx.doi.org/10.1155/2014/863647 Text en Copyright © 2014 T. A. Olajide et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Olajide, T. A.
Agodirin, S. O.
Ojewola, R. W.
Akanbi, O. O.
Solaja, T. O.
Odesanya, Johnson Oluremi
Ariyibi, O. O.
Jejunal Choristoma: A Very Rare Cause of Abdominal Pain in Children
title Jejunal Choristoma: A Very Rare Cause of Abdominal Pain in Children
title_full Jejunal Choristoma: A Very Rare Cause of Abdominal Pain in Children
title_fullStr Jejunal Choristoma: A Very Rare Cause of Abdominal Pain in Children
title_full_unstemmed Jejunal Choristoma: A Very Rare Cause of Abdominal Pain in Children
title_short Jejunal Choristoma: A Very Rare Cause of Abdominal Pain in Children
title_sort jejunal choristoma: a very rare cause of abdominal pain in children
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3910446/
https://www.ncbi.nlm.nih.gov/pubmed/24511408
http://dx.doi.org/10.1155/2014/863647
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