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A Rare Cause of Dysphagia and Weight Loss

Mixed connective tissue disease (MCTD) is a rare connective tissue disorder with clinical features that overlap with systemic lupus erythematous, systemic sclerosis, and polymyositis. We report the case of a patient who presented with dysphagia, 25-lb weight loss, difficulty opening her mouth, and j...

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Autores principales: Gyorffy, Janelle B., Marowske, Johanna, Gancayco, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244109/
https://www.ncbi.nlm.nih.gov/pubmed/30483043
http://dx.doi.org/10.1159/000493919
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author Gyorffy, Janelle B.
Marowske, Johanna
Gancayco, John
author_facet Gyorffy, Janelle B.
Marowske, Johanna
Gancayco, John
author_sort Gyorffy, Janelle B.
collection PubMed
description Mixed connective tissue disease (MCTD) is a rare connective tissue disorder with clinical features that overlap with systemic lupus erythematous, systemic sclerosis, and polymyositis. We report the case of a patient who presented with dysphagia, 25-lb weight loss, difficulty opening her mouth, and joint pain. Dysphagia workup showed a normal barium swallow and normal-appearing EGD but esophageal manometry consistent with severe dysmotility. Through further laboratory and imaging studies, the patient met the diagnostic criteria for MCTD. She had marked improvement in her dysphagia with steroids, biologic therapy, and intravenous immunoglobulin.
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spelling pubmed-62441092018-11-27 A Rare Cause of Dysphagia and Weight Loss Gyorffy, Janelle B. Marowske, Johanna Gancayco, John Case Rep Gastroenterol Single Case Mixed connective tissue disease (MCTD) is a rare connective tissue disorder with clinical features that overlap with systemic lupus erythematous, systemic sclerosis, and polymyositis. We report the case of a patient who presented with dysphagia, 25-lb weight loss, difficulty opening her mouth, and joint pain. Dysphagia workup showed a normal barium swallow and normal-appearing EGD but esophageal manometry consistent with severe dysmotility. Through further laboratory and imaging studies, the patient met the diagnostic criteria for MCTD. She had marked improvement in her dysphagia with steroids, biologic therapy, and intravenous immunoglobulin. S. Karger AG 2018-11-01 /pmc/articles/PMC6244109/ /pubmed/30483043 http://dx.doi.org/10.1159/000493919 Text en Copyright © 2018 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Single Case
Gyorffy, Janelle B.
Marowske, Johanna
Gancayco, John
A Rare Cause of Dysphagia and Weight Loss
title A Rare Cause of Dysphagia and Weight Loss
title_full A Rare Cause of Dysphagia and Weight Loss
title_fullStr A Rare Cause of Dysphagia and Weight Loss
title_full_unstemmed A Rare Cause of Dysphagia and Weight Loss
title_short A Rare Cause of Dysphagia and Weight Loss
title_sort rare cause of dysphagia and weight loss
topic Single Case
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244109/
https://www.ncbi.nlm.nih.gov/pubmed/30483043
http://dx.doi.org/10.1159/000493919
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