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Progression of Jackhammer Esophagus to Type II Achalasia

It has been suggested that patients with certain motility disorders may progress overtime to develop achalasia. We describe a 66 year-old woman who presented with dysphagia for solids and liquids for a period of 18 months. Her initial workup showed normal endoscopy and non-specific esophageal motili...

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Autores principales: Abdallah, Jason, Fass, Ronnie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Neurogastroenterology and Motility 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4699733/
https://www.ncbi.nlm.nih.gov/pubmed/26717932
http://dx.doi.org/10.5056/jnm15162
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author Abdallah, Jason
Fass, Ronnie
author_facet Abdallah, Jason
Fass, Ronnie
author_sort Abdallah, Jason
collection PubMed
description It has been suggested that patients with certain motility disorders may progress overtime to develop achalasia. We describe a 66 year-old woman who presented with dysphagia for solids and liquids for a period of 18 months. Her initial workup showed normal endoscopy and non-specific esophageal motility disorder on conventional manometry. Six months later, due to persistence of symptoms, the patient underwent a high resolution esophageal manometry (HREM) demonstrating jackhammer esophagus. The patient was treated with a high dose proton pump inhibitor but without resolution of her symptoms. During the last year, the patient reported repeated episodes of food regurgitation and a significant weight loss. A repeat HREM revealed type II achalasia. Multiple case reports, and only a few prospective studies have demonstrated progression from certain esophageal motility disorders to achalasia. However, this report is the first to describe a case of jackhammer esophagus progressing to type II achalasia.
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spelling pubmed-46997332016-01-05 Progression of Jackhammer Esophagus to Type II Achalasia Abdallah, Jason Fass, Ronnie J Neurogastroenterol Motil Case Report It has been suggested that patients with certain motility disorders may progress overtime to develop achalasia. We describe a 66 year-old woman who presented with dysphagia for solids and liquids for a period of 18 months. Her initial workup showed normal endoscopy and non-specific esophageal motility disorder on conventional manometry. Six months later, due to persistence of symptoms, the patient underwent a high resolution esophageal manometry (HREM) demonstrating jackhammer esophagus. The patient was treated with a high dose proton pump inhibitor but without resolution of her symptoms. During the last year, the patient reported repeated episodes of food regurgitation and a significant weight loss. A repeat HREM revealed type II achalasia. Multiple case reports, and only a few prospective studies have demonstrated progression from certain esophageal motility disorders to achalasia. However, this report is the first to describe a case of jackhammer esophagus progressing to type II achalasia. Korean Society of Neurogastroenterology and Motility 2016-01 2016-01-30 /pmc/articles/PMC4699733/ /pubmed/26717932 http://dx.doi.org/10.5056/jnm15162 Text en © 2016 The Korean Society of Neurogastroenterology and Motility This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Abdallah, Jason
Fass, Ronnie
Progression of Jackhammer Esophagus to Type II Achalasia
title Progression of Jackhammer Esophagus to Type II Achalasia
title_full Progression of Jackhammer Esophagus to Type II Achalasia
title_fullStr Progression of Jackhammer Esophagus to Type II Achalasia
title_full_unstemmed Progression of Jackhammer Esophagus to Type II Achalasia
title_short Progression of Jackhammer Esophagus to Type II Achalasia
title_sort progression of jackhammer esophagus to type ii achalasia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4699733/
https://www.ncbi.nlm.nih.gov/pubmed/26717932
http://dx.doi.org/10.5056/jnm15162
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