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Late-onset congenital diaphragmatic hernia: A case report()
INTRODUCTION: A Bochdalek hernia is a posterior congenital defect of the diaphragm, usually on the left hemidiafragm, caused by a lack of closure of the pleuroperitoneal canal between the eighth and tenth week of fetal life during the embryonic development. It typically presents in the neonatal peri...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3825969/ https://www.ncbi.nlm.nih.gov/pubmed/24055915 http://dx.doi.org/10.1016/j.ijscr.2013.07.034 |
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author | Vega, Marcel Tapia Maldonado, Regina Herbas Vega, Gretty Tapia Vega, Alenka Tapia Liévano, Elisafat Arce Velázquez, Paulina Moctezuma |
author_facet | Vega, Marcel Tapia Maldonado, Regina Herbas Vega, Gretty Tapia Vega, Alenka Tapia Liévano, Elisafat Arce Velázquez, Paulina Moctezuma |
author_sort | Vega, Marcel Tapia |
collection | PubMed |
description | INTRODUCTION: A Bochdalek hernia is a posterior congenital defect of the diaphragm, usually on the left hemidiafragm, caused by a lack of closure of the pleuroperitoneal canal between the eighth and tenth week of fetal life during the embryonic development. It typically presents in the neonatal period with severe respiratory failure. PRESENTATION OF CASE: In this paper we present a 35 year old man with a 5-year history of episodes of severe dyspnea who arrived to the emergency room, during his medical work-up we incidentally found an intrathoracic gastric bubble, a laparoscopy was performed, founding a necrotic stomach and for defect correction. DISCUSSION: This pathology is infrequent in adults, among this age group, there are two different clinical presentations: asymptomatic patients who are diagnosed incidentally when abdominal organs are found in the thorax in a chest X-ray, and symptomatic patients due to side effects of incarceration, strangulation, hemorrhage and visceral perforation in the chest cavity. CONCLUSION: Diaphragmatic hernias are rare among adult population, and they are usually asymptomatic, in this case we presented a symptomatic patient, diagnosed with a chest X-ray and treated surgically. The surgical approach for the resolution of this pathology is variable and it depends on the presence and severity of visceral complications. |
format | Online Article Text |
id | pubmed-3825969 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-38259692013-11-13 Late-onset congenital diaphragmatic hernia: A case report() Vega, Marcel Tapia Maldonado, Regina Herbas Vega, Gretty Tapia Vega, Alenka Tapia Liévano, Elisafat Arce Velázquez, Paulina Moctezuma Int J Surg Case Rep Article INTRODUCTION: A Bochdalek hernia is a posterior congenital defect of the diaphragm, usually on the left hemidiafragm, caused by a lack of closure of the pleuroperitoneal canal between the eighth and tenth week of fetal life during the embryonic development. It typically presents in the neonatal period with severe respiratory failure. PRESENTATION OF CASE: In this paper we present a 35 year old man with a 5-year history of episodes of severe dyspnea who arrived to the emergency room, during his medical work-up we incidentally found an intrathoracic gastric bubble, a laparoscopy was performed, founding a necrotic stomach and for defect correction. DISCUSSION: This pathology is infrequent in adults, among this age group, there are two different clinical presentations: asymptomatic patients who are diagnosed incidentally when abdominal organs are found in the thorax in a chest X-ray, and symptomatic patients due to side effects of incarceration, strangulation, hemorrhage and visceral perforation in the chest cavity. CONCLUSION: Diaphragmatic hernias are rare among adult population, and they are usually asymptomatic, in this case we presented a symptomatic patient, diagnosed with a chest X-ray and treated surgically. The surgical approach for the resolution of this pathology is variable and it depends on the presence and severity of visceral complications. Elsevier 2013-08-28 /pmc/articles/PMC3825969/ /pubmed/24055915 http://dx.doi.org/10.1016/j.ijscr.2013.07.034 Text en © 2013 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-No Derivative Works License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Article Vega, Marcel Tapia Maldonado, Regina Herbas Vega, Gretty Tapia Vega, Alenka Tapia Liévano, Elisafat Arce Velázquez, Paulina Moctezuma Late-onset congenital diaphragmatic hernia: A case report() |
title | Late-onset congenital diaphragmatic hernia: A case report() |
title_full | Late-onset congenital diaphragmatic hernia: A case report() |
title_fullStr | Late-onset congenital diaphragmatic hernia: A case report() |
title_full_unstemmed | Late-onset congenital diaphragmatic hernia: A case report() |
title_short | Late-onset congenital diaphragmatic hernia: A case report() |
title_sort | late-onset congenital diaphragmatic hernia: a case report() |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3825969/ https://www.ncbi.nlm.nih.gov/pubmed/24055915 http://dx.doi.org/10.1016/j.ijscr.2013.07.034 |
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