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Giant Meckel’s Diverticulum in a 9-Year-Old Boy: An Unusual Presentation With Isolated Faltering Growth

Meckel’s diverticulum is the most common congenital gastrointestinal abnormality. Clinical presentation is normally in childhood with either hemorrhage or an acute surgical abdomen. The much rarer giant Meckel’s diverticulum is associated with a more varied clinical presentation. In this case report...

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Autores principales: Rout, Alexandra, Morreau, Phil, Bird, Helen, Roberts, Amin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158295/
https://www.ncbi.nlm.nih.gov/pubmed/37168630
http://dx.doi.org/10.1097/PG9.0000000000000208
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author Rout, Alexandra
Morreau, Phil
Bird, Helen
Roberts, Amin
author_facet Rout, Alexandra
Morreau, Phil
Bird, Helen
Roberts, Amin
author_sort Rout, Alexandra
collection PubMed
description Meckel’s diverticulum is the most common congenital gastrointestinal abnormality. Clinical presentation is normally in childhood with either hemorrhage or an acute surgical abdomen. The much rarer giant Meckel’s diverticulum is associated with a more varied clinical presentation. In this case report, we provide a unique example of presentation with isolated faltering growth related to a giant Meckel’s diverticulum in a young boy. We discuss the diagnostic process, imaging modalities, and subsequent surgical procedure.
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spelling pubmed-101582952023-05-09 Giant Meckel’s Diverticulum in a 9-Year-Old Boy: An Unusual Presentation With Isolated Faltering Growth Rout, Alexandra Morreau, Phil Bird, Helen Roberts, Amin JPGN Rep Case Report Meckel’s diverticulum is the most common congenital gastrointestinal abnormality. Clinical presentation is normally in childhood with either hemorrhage or an acute surgical abdomen. The much rarer giant Meckel’s diverticulum is associated with a more varied clinical presentation. In this case report, we provide a unique example of presentation with isolated faltering growth related to a giant Meckel’s diverticulum in a young boy. We discuss the diagnostic process, imaging modalities, and subsequent surgical procedure. Lippincott Williams & Wilkins, Inc. 2022-06-21 /pmc/articles/PMC10158295/ /pubmed/37168630 http://dx.doi.org/10.1097/PG9.0000000000000208 Text en Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Case Report
Rout, Alexandra
Morreau, Phil
Bird, Helen
Roberts, Amin
Giant Meckel’s Diverticulum in a 9-Year-Old Boy: An Unusual Presentation With Isolated Faltering Growth
title Giant Meckel’s Diverticulum in a 9-Year-Old Boy: An Unusual Presentation With Isolated Faltering Growth
title_full Giant Meckel’s Diverticulum in a 9-Year-Old Boy: An Unusual Presentation With Isolated Faltering Growth
title_fullStr Giant Meckel’s Diverticulum in a 9-Year-Old Boy: An Unusual Presentation With Isolated Faltering Growth
title_full_unstemmed Giant Meckel’s Diverticulum in a 9-Year-Old Boy: An Unusual Presentation With Isolated Faltering Growth
title_short Giant Meckel’s Diverticulum in a 9-Year-Old Boy: An Unusual Presentation With Isolated Faltering Growth
title_sort giant meckel’s diverticulum in a 9-year-old boy: an unusual presentation with isolated faltering growth
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158295/
https://www.ncbi.nlm.nih.gov/pubmed/37168630
http://dx.doi.org/10.1097/PG9.0000000000000208
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