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Refractory Pediatric Fibrostenotic Eosinophilic Esophagitis Treated With Dupilumab

Eosinophilic esophagitis (EoE) is a progressive inflammatory disease of the esophagus. Untreated or uncontrolled disease over time can lead to the development of fibrosis and formation of strictures. Once the patient develops strictures, it is difficult to treat with the available medical therapies...

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Autores principales: Gangadharan Nambiar, Gopinathan, Rahhal, Riad, Davis, Benjamin P., Xiong, Yiqin, Cheung, Donna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9663132/
https://www.ncbi.nlm.nih.gov/pubmed/36382335
http://dx.doi.org/10.14309/crj.0000000000000887
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author Gangadharan Nambiar, Gopinathan
Rahhal, Riad
Davis, Benjamin P.
Xiong, Yiqin
Cheung, Donna
author_facet Gangadharan Nambiar, Gopinathan
Rahhal, Riad
Davis, Benjamin P.
Xiong, Yiqin
Cheung, Donna
author_sort Gangadharan Nambiar, Gopinathan
collection PubMed
description Eosinophilic esophagitis (EoE) is a progressive inflammatory disease of the esophagus. Untreated or uncontrolled disease over time can lead to the development of fibrosis and formation of strictures. Once the patient develops strictures, it is difficult to treat with the available medical therapies and will often require esophageal dilations. The Food and Drug Administration recently approved dupilumab for the treatment of EoE in patients older than 12 years. The clinical trials excluded patients with esophageal strictures. We describe a case of EoE with fibrostenotic stricture who had stricture resolution while on dupilumab therapy.
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spelling pubmed-96631322022-11-14 Refractory Pediatric Fibrostenotic Eosinophilic Esophagitis Treated With Dupilumab Gangadharan Nambiar, Gopinathan Rahhal, Riad Davis, Benjamin P. Xiong, Yiqin Cheung, Donna ACG Case Rep J Case Report Eosinophilic esophagitis (EoE) is a progressive inflammatory disease of the esophagus. Untreated or uncontrolled disease over time can lead to the development of fibrosis and formation of strictures. Once the patient develops strictures, it is difficult to treat with the available medical therapies and will often require esophageal dilations. The Food and Drug Administration recently approved dupilumab for the treatment of EoE in patients older than 12 years. The clinical trials excluded patients with esophageal strictures. We describe a case of EoE with fibrostenotic stricture who had stricture resolution while on dupilumab therapy. Wolters Kluwer 2022-11-11 /pmc/articles/PMC9663132/ /pubmed/36382335 http://dx.doi.org/10.14309/crj.0000000000000887 Text en © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Case Report
Gangadharan Nambiar, Gopinathan
Rahhal, Riad
Davis, Benjamin P.
Xiong, Yiqin
Cheung, Donna
Refractory Pediatric Fibrostenotic Eosinophilic Esophagitis Treated With Dupilumab
title Refractory Pediatric Fibrostenotic Eosinophilic Esophagitis Treated With Dupilumab
title_full Refractory Pediatric Fibrostenotic Eosinophilic Esophagitis Treated With Dupilumab
title_fullStr Refractory Pediatric Fibrostenotic Eosinophilic Esophagitis Treated With Dupilumab
title_full_unstemmed Refractory Pediatric Fibrostenotic Eosinophilic Esophagitis Treated With Dupilumab
title_short Refractory Pediatric Fibrostenotic Eosinophilic Esophagitis Treated With Dupilumab
title_sort refractory pediatric fibrostenotic eosinophilic esophagitis treated with dupilumab
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9663132/
https://www.ncbi.nlm.nih.gov/pubmed/36382335
http://dx.doi.org/10.14309/crj.0000000000000887
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