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Chilaiditi syndrome in pediatric patients - Symptomatic hepatodiaphragmatic interposition of colon: A case report and review of literature
BACKGROUND: Chilaiditi syndrome is a rare disorder characterized by the hepatodiaphragmatic interposition of the intestine. CASE SUMMARY: Here we report a case of a 12-year-old male who was admitted to the pediatric intensive care unit secondary to abdominal pain and severe respiratory distress. He...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8085720/ https://www.ncbi.nlm.nih.gov/pubmed/33972924 http://dx.doi.org/10.5409/wjcp.v10.i3.40 |
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author | Caicedo, Luis Wasuwanich, Paul Rivera, Andrés Lopez, Maria S Karnsakul, Wikrom |
author_facet | Caicedo, Luis Wasuwanich, Paul Rivera, Andrés Lopez, Maria S Karnsakul, Wikrom |
author_sort | Caicedo, Luis |
collection | PubMed |
description | BACKGROUND: Chilaiditi syndrome is a rare disorder characterized by the hepatodiaphragmatic interposition of the intestine. CASE SUMMARY: Here we report a case of a 12-year-old male who was admitted to the pediatric intensive care unit secondary to abdominal pain and severe respiratory distress. He was treated conservatively but the symptoms persisted requiring a surgical approach. While there have been several cases of Chilaiditi syndrome reported in adults, there is a scarcity of cases reported in the pediatric population. Our review of the literature found only 30 pediatric cases, including our reported case, with Chilaiditi syndrome, 19 (63%) of which were male. The median age of diagnosis was 4.5 years old with an interquartile range of 2.0-10.0 years. In our review, we found that the most common predisposing factors in children are aerophagia (12/30 cases) and constipation (13/30 cases). Ninety percent of the cases presented with complete intestinal interposition, in 100% of which, the colon was involved. Three of the 30 cases were associated with volvulus. CONCLUSION: In the pediatric population, conservative (21/30 cases) and surgical (8/30 cases) treatment approaches have produced satisfactory outcomes for all the patients, regardless of approach. |
format | Online Article Text |
id | pubmed-8085720 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-80857202021-05-09 Chilaiditi syndrome in pediatric patients - Symptomatic hepatodiaphragmatic interposition of colon: A case report and review of literature Caicedo, Luis Wasuwanich, Paul Rivera, Andrés Lopez, Maria S Karnsakul, Wikrom World J Clin Pediatr Case Report BACKGROUND: Chilaiditi syndrome is a rare disorder characterized by the hepatodiaphragmatic interposition of the intestine. CASE SUMMARY: Here we report a case of a 12-year-old male who was admitted to the pediatric intensive care unit secondary to abdominal pain and severe respiratory distress. He was treated conservatively but the symptoms persisted requiring a surgical approach. While there have been several cases of Chilaiditi syndrome reported in adults, there is a scarcity of cases reported in the pediatric population. Our review of the literature found only 30 pediatric cases, including our reported case, with Chilaiditi syndrome, 19 (63%) of which were male. The median age of diagnosis was 4.5 years old with an interquartile range of 2.0-10.0 years. In our review, we found that the most common predisposing factors in children are aerophagia (12/30 cases) and constipation (13/30 cases). Ninety percent of the cases presented with complete intestinal interposition, in 100% of which, the colon was involved. Three of the 30 cases were associated with volvulus. CONCLUSION: In the pediatric population, conservative (21/30 cases) and surgical (8/30 cases) treatment approaches have produced satisfactory outcomes for all the patients, regardless of approach. Baishideng Publishing Group Inc 2021-05-09 /pmc/articles/PMC8085720/ /pubmed/33972924 http://dx.doi.org/10.5409/wjcp.v10.i3.40 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Case Report Caicedo, Luis Wasuwanich, Paul Rivera, Andrés Lopez, Maria S Karnsakul, Wikrom Chilaiditi syndrome in pediatric patients - Symptomatic hepatodiaphragmatic interposition of colon: A case report and review of literature |
title | Chilaiditi syndrome in pediatric patients - Symptomatic hepatodiaphragmatic interposition of colon: A case report and review of literature |
title_full | Chilaiditi syndrome in pediatric patients - Symptomatic hepatodiaphragmatic interposition of colon: A case report and review of literature |
title_fullStr | Chilaiditi syndrome in pediatric patients - Symptomatic hepatodiaphragmatic interposition of colon: A case report and review of literature |
title_full_unstemmed | Chilaiditi syndrome in pediatric patients - Symptomatic hepatodiaphragmatic interposition of colon: A case report and review of literature |
title_short | Chilaiditi syndrome in pediatric patients - Symptomatic hepatodiaphragmatic interposition of colon: A case report and review of literature |
title_sort | chilaiditi syndrome in pediatric patients - symptomatic hepatodiaphragmatic interposition of colon: a case report and review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8085720/ https://www.ncbi.nlm.nih.gov/pubmed/33972924 http://dx.doi.org/10.5409/wjcp.v10.i3.40 |
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