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Esophageal Pharmacobezoar in a Patient with Achalasia: A Case Report

A few cases with esophageal bezoar have been reported in achalasia. We describe here a rare case of esophageal pharmacobezoar after ingestion of ferrous sulfate capsules in a patient with achalasia. A 29-year-old woman presented with severe dysphagia since five days earlier. She had history of achal...

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Autor principal: Tavakkoli, Hamid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iranian Association of Gastroerterology and Hepatology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819961/
https://www.ncbi.nlm.nih.gov/pubmed/31687117
http://dx.doi.org/10.15171/mejdd.2019.145
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author Tavakkoli, Hamid
author_facet Tavakkoli, Hamid
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description A few cases with esophageal bezoar have been reported in achalasia. We describe here a rare case of esophageal pharmacobezoar after ingestion of ferrous sulfate capsules in a patient with achalasia. A 29-year-old woman presented with severe dysphagia since five days earlier. She had history of achalasia since 3 years ago but had refused any treatment option. After about 3 weeks of ferrous sulfate capsules ingestion, she developed severe dysphagia and was referred to a gastroenterologist. Physical examination was unremarkable. A barium swallow revealed dilated esophagus and bird’s beak appearance. Esophagogastroduodenoscopy (EGD) showed dilated esophagus and soft black color bezoar in distal part of esophagus. The bezoar was retrieved with basket. In the next endoscopic session, achalasia balloon dilation was successfully applied. Ferrous sulfate capsules can cause pharmacobezoar in patients with achalasia. Esophageal bezoar should be considered in differential diagnosis of untreated achalasia and acute exacerbation of dysphagia.
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spelling pubmed-68199612019-11-04 Esophageal Pharmacobezoar in a Patient with Achalasia: A Case Report Tavakkoli, Hamid Middle East J Dig Dis Case Report A few cases with esophageal bezoar have been reported in achalasia. We describe here a rare case of esophageal pharmacobezoar after ingestion of ferrous sulfate capsules in a patient with achalasia. A 29-year-old woman presented with severe dysphagia since five days earlier. She had history of achalasia since 3 years ago but had refused any treatment option. After about 3 weeks of ferrous sulfate capsules ingestion, she developed severe dysphagia and was referred to a gastroenterologist. Physical examination was unremarkable. A barium swallow revealed dilated esophagus and bird’s beak appearance. Esophagogastroduodenoscopy (EGD) showed dilated esophagus and soft black color bezoar in distal part of esophagus. The bezoar was retrieved with basket. In the next endoscopic session, achalasia balloon dilation was successfully applied. Ferrous sulfate capsules can cause pharmacobezoar in patients with achalasia. Esophageal bezoar should be considered in differential diagnosis of untreated achalasia and acute exacerbation of dysphagia. Iranian Association of Gastroerterology and Hepatology 2019-07 2019-06-10 /pmc/articles/PMC6819961/ /pubmed/31687117 http://dx.doi.org/10.15171/mejdd.2019.145 Text en © 2019 The Author(s) This work is published by Middle East Journal of Digestive Diseaes as an open access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by-nc/4.0/). Non-commercial uses of the work are permitted, provided the original work is properly cited.
spellingShingle Case Report
Tavakkoli, Hamid
Esophageal Pharmacobezoar in a Patient with Achalasia: A Case Report
title Esophageal Pharmacobezoar in a Patient with Achalasia: A Case Report
title_full Esophageal Pharmacobezoar in a Patient with Achalasia: A Case Report
title_fullStr Esophageal Pharmacobezoar in a Patient with Achalasia: A Case Report
title_full_unstemmed Esophageal Pharmacobezoar in a Patient with Achalasia: A Case Report
title_short Esophageal Pharmacobezoar in a Patient with Achalasia: A Case Report
title_sort esophageal pharmacobezoar in a patient with achalasia: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819961/
https://www.ncbi.nlm.nih.gov/pubmed/31687117
http://dx.doi.org/10.15171/mejdd.2019.145
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