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Boerhaave’s syndrome as an initial presentation of eosinophilic esophagitis: a case series

BACKGROUND: Prior studies report esophageal rupture following endoscopy or bolus impaction in eosinophilic esophagitis (EoE). The purpose of this study is to add new information to available evidence defining the clinical spectrum of spontaneous rupture (Boerhaave’s syndrome) associated with vomitin...

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Autores principales: Jackson, Whitney E., Mehendiratta, Vaibhav, Palazzo, Juan, DiMarino, Anthony J., Quirk, Daniel M., Cohen, Sidney
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hellenic Society of Gastroenterology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3959943/
https://www.ncbi.nlm.nih.gov/pubmed/24714779
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author Jackson, Whitney E.
Mehendiratta, Vaibhav
Palazzo, Juan
DiMarino, Anthony J.
Quirk, Daniel M.
Cohen, Sidney
author_facet Jackson, Whitney E.
Mehendiratta, Vaibhav
Palazzo, Juan
DiMarino, Anthony J.
Quirk, Daniel M.
Cohen, Sidney
author_sort Jackson, Whitney E.
collection PubMed
description BACKGROUND: Prior studies report esophageal rupture following endoscopy or bolus impaction in eosinophilic esophagitis (EoE). The purpose of this study is to add new information to available evidence defining the clinical spectrum of spontaneous rupture (Boerhaave’s syndrome) associated with vomiting in EoE. METHODS: A retrospective search of inpatient and outpatient records was conducted from January 2001 to January 2011. A faculty member in pathology blindly reviewed all esophageal biopsy specimens. EoE was defined as 15 or more eosinophils in at least 2 high-power fields (hpfs) or 25 or more eosinophils in any single HPF. RESULTS: In ten years, 447 patients were identified with a diagnosis of EoE. Of these, four patients presented with Boerhaave’s syndrome in the setting of EoE. None of the patients had an established diagnosis of EoE prior to presentation. All cases presented with a triad of vomiting, chest pain and pneumomediastinum. In two patients, water-soluble contrast extravasation prompted surgical intervention (50%). Full thickness surgical specimen provides a unique opportunity to show eosinophils in the muscularis propria. Intraepithelial eosinophil infiltration was seen on all mucosal biopsies (>25/hpf) with significant improvement after steroid (topical or systemic) treatment. CONCLUSIONS: Spontaneous esophageal rupture is a rare (4/447, less than 1%) but critical presentation of EoE manifesting with vomiting, chest pain and pneumomediastinum. Surgery is required if extravasation is seen with water-soluble contrast. We suggest that EoE may be a transmural disease in some patients, thus making the esophageal wall susceptible to spontaneous rupture with vomiting (Boerhaave’s syndrome).
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spelling pubmed-39599432014-04-07 Boerhaave’s syndrome as an initial presentation of eosinophilic esophagitis: a case series Jackson, Whitney E. Mehendiratta, Vaibhav Palazzo, Juan DiMarino, Anthony J. Quirk, Daniel M. Cohen, Sidney Ann Gastroenterol Case Series BACKGROUND: Prior studies report esophageal rupture following endoscopy or bolus impaction in eosinophilic esophagitis (EoE). The purpose of this study is to add new information to available evidence defining the clinical spectrum of spontaneous rupture (Boerhaave’s syndrome) associated with vomiting in EoE. METHODS: A retrospective search of inpatient and outpatient records was conducted from January 2001 to January 2011. A faculty member in pathology blindly reviewed all esophageal biopsy specimens. EoE was defined as 15 or more eosinophils in at least 2 high-power fields (hpfs) or 25 or more eosinophils in any single HPF. RESULTS: In ten years, 447 patients were identified with a diagnosis of EoE. Of these, four patients presented with Boerhaave’s syndrome in the setting of EoE. None of the patients had an established diagnosis of EoE prior to presentation. All cases presented with a triad of vomiting, chest pain and pneumomediastinum. In two patients, water-soluble contrast extravasation prompted surgical intervention (50%). Full thickness surgical specimen provides a unique opportunity to show eosinophils in the muscularis propria. Intraepithelial eosinophil infiltration was seen on all mucosal biopsies (>25/hpf) with significant improvement after steroid (topical or systemic) treatment. CONCLUSIONS: Spontaneous esophageal rupture is a rare (4/447, less than 1%) but critical presentation of EoE manifesting with vomiting, chest pain and pneumomediastinum. Surgery is required if extravasation is seen with water-soluble contrast. We suggest that EoE may be a transmural disease in some patients, thus making the esophageal wall susceptible to spontaneous rupture with vomiting (Boerhaave’s syndrome). Hellenic Society of Gastroenterology 2013 /pmc/articles/PMC3959943/ /pubmed/24714779 Text en Copyright: © Hellenic Society of Gastroenterology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Series
Jackson, Whitney E.
Mehendiratta, Vaibhav
Palazzo, Juan
DiMarino, Anthony J.
Quirk, Daniel M.
Cohen, Sidney
Boerhaave’s syndrome as an initial presentation of eosinophilic esophagitis: a case series
title Boerhaave’s syndrome as an initial presentation of eosinophilic esophagitis: a case series
title_full Boerhaave’s syndrome as an initial presentation of eosinophilic esophagitis: a case series
title_fullStr Boerhaave’s syndrome as an initial presentation of eosinophilic esophagitis: a case series
title_full_unstemmed Boerhaave’s syndrome as an initial presentation of eosinophilic esophagitis: a case series
title_short Boerhaave’s syndrome as an initial presentation of eosinophilic esophagitis: a case series
title_sort boerhaave’s syndrome as an initial presentation of eosinophilic esophagitis: a case series
topic Case Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3959943/
https://www.ncbi.nlm.nih.gov/pubmed/24714779
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