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A rare case of oesophageal rupture: Boerhaave's syndrome

A 70-year-old patient was referred to our emergency department with severe retrosternal pain after forceful vomiting. Computed tomography (CT) scan revealed a left-sided oesophageal rupture with accompanying pneumomediastinum and bilateral pleural effusions. Conservative treatment with cessation of...

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Autores principales: van der Weg, Gerben, Wikkeling, Marald, van Leeuwen, Maarten, ter Avest, Ewoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215748/
https://www.ncbi.nlm.nih.gov/pubmed/25364474
http://dx.doi.org/10.1186/s12245-014-0027-2
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author van der Weg, Gerben
Wikkeling, Marald
van Leeuwen, Maarten
ter Avest, Ewoud
author_facet van der Weg, Gerben
Wikkeling, Marald
van Leeuwen, Maarten
ter Avest, Ewoud
author_sort van der Weg, Gerben
collection PubMed
description A 70-year-old patient was referred to our emergency department with severe retrosternal pain after forceful vomiting. Computed tomography (CT) scan revealed a left-sided oesophageal rupture with accompanying pneumomediastinum and bilateral pleural effusions. Conservative treatment with cessation of oral intake, intravenous broad-spectrum antibiotics, parenteral fluids and nutrition and left sided tube thoracostomy was initiated initially. After 5 days, however, the patient deteriorated. Follow-up CT scan demonstrated a mediastinal fluid collection as well as loculated pleural empyema. Open thoracotomy with mediastinal debridement and pleural drainage was performed, after which he made a slow but full recovery. Spontaneous oesophageal rupture due to an abrupt rise in intraluminal pressure caused by vomiting is also known as Boerhaave's syndrome. It is a rare but potentially life-threatening condition. Many patients present with atypical symptoms, and therefore, physicians should have a high index of suspicion in any patient presenting with vomiting and retrosternal pain. When Boerhaave's syndrome is suspected, a CT scan of the thorax and upper abdomen should be performed since treatment depends on clinical and radiological findings. Conservative management (cessation of oral intake, nasogastric decompression, administration of intravenous fluids and parenteral nutrition, intravenous broad-spectrum antibiotics and proton pump inhibitors and tube thoracostomies) may only be considered in patients with a contained rupture without systematic symptoms of infection. In these patients, endoscopic bridging of the tear with a self-expandable stent is also an option. Primary surgical repair (either by thoracotomy or by video assisted thoracoscopy (VATS)) should be considered when patients present with sepsis and/or large non-contained leaks or with severe mediastinal decontamination.
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spelling pubmed-42157482014-10-31 A rare case of oesophageal rupture: Boerhaave's syndrome van der Weg, Gerben Wikkeling, Marald van Leeuwen, Maarten ter Avest, Ewoud Int J Emerg Med Case Report A 70-year-old patient was referred to our emergency department with severe retrosternal pain after forceful vomiting. Computed tomography (CT) scan revealed a left-sided oesophageal rupture with accompanying pneumomediastinum and bilateral pleural effusions. Conservative treatment with cessation of oral intake, intravenous broad-spectrum antibiotics, parenteral fluids and nutrition and left sided tube thoracostomy was initiated initially. After 5 days, however, the patient deteriorated. Follow-up CT scan demonstrated a mediastinal fluid collection as well as loculated pleural empyema. Open thoracotomy with mediastinal debridement and pleural drainage was performed, after which he made a slow but full recovery. Spontaneous oesophageal rupture due to an abrupt rise in intraluminal pressure caused by vomiting is also known as Boerhaave's syndrome. It is a rare but potentially life-threatening condition. Many patients present with atypical symptoms, and therefore, physicians should have a high index of suspicion in any patient presenting with vomiting and retrosternal pain. When Boerhaave's syndrome is suspected, a CT scan of the thorax and upper abdomen should be performed since treatment depends on clinical and radiological findings. Conservative management (cessation of oral intake, nasogastric decompression, administration of intravenous fluids and parenteral nutrition, intravenous broad-spectrum antibiotics and proton pump inhibitors and tube thoracostomies) may only be considered in patients with a contained rupture without systematic symptoms of infection. In these patients, endoscopic bridging of the tear with a self-expandable stent is also an option. Primary surgical repair (either by thoracotomy or by video assisted thoracoscopy (VATS)) should be considered when patients present with sepsis and/or large non-contained leaks or with severe mediastinal decontamination. Springer 2014-07-01 /pmc/articles/PMC4215748/ /pubmed/25364474 http://dx.doi.org/10.1186/s12245-014-0027-2 Text en Copyright © 2014 van der Weg et al.; licensee Springer http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly .
spellingShingle Case Report
van der Weg, Gerben
Wikkeling, Marald
van Leeuwen, Maarten
ter Avest, Ewoud
A rare case of oesophageal rupture: Boerhaave's syndrome
title A rare case of oesophageal rupture: Boerhaave's syndrome
title_full A rare case of oesophageal rupture: Boerhaave's syndrome
title_fullStr A rare case of oesophageal rupture: Boerhaave's syndrome
title_full_unstemmed A rare case of oesophageal rupture: Boerhaave's syndrome
title_short A rare case of oesophageal rupture: Boerhaave's syndrome
title_sort rare case of oesophageal rupture: boerhaave's syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215748/
https://www.ncbi.nlm.nih.gov/pubmed/25364474
http://dx.doi.org/10.1186/s12245-014-0027-2
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