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Successful Montelukast Treatment in an Infant with Steroid-Resistant Eosinophilic Colitis
Eosinophilic colitis (EC) belongs to a group of idiopathic diseases called eosinophilic gastrointestinal disorders, which are characterized by eosinophil-predominant inflammation in the gastrointestinal tract. Corticosteroids is the first-line pharmacotherapy for EC refractory to diet therapy. We re...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077466/ https://www.ncbi.nlm.nih.gov/pubmed/33976616 http://dx.doi.org/10.1159/000513146 |
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author | Wang, Nai-Wei Hsieh, Hsuan Yang, Yao-Jong |
author_facet | Wang, Nai-Wei Hsieh, Hsuan Yang, Yao-Jong |
author_sort | Wang, Nai-Wei |
collection | PubMed |
description | Eosinophilic colitis (EC) belongs to a group of idiopathic diseases called eosinophilic gastrointestinal disorders, which are characterized by eosinophil-predominant inflammation in the gastrointestinal tract. Corticosteroids is the first-line pharmacotherapy for EC refractory to diet therapy. We report an infant with steroid-resistant EC, who successfully returned to a healthy growth trajectory under the combined therapy of montelukast and ketotifen. An 8-month-old boy presented with bloody diarrhea, anemia, and failure to thrive (FTT) that started 6 days after birth. The patient has no known allergies. A trial of elementary diet was unsuccessful. The results of several stool cultures were unremarkable. Similarly, lower gastrointestinal series failed to identify anything significant. At 3 months of age, an esophagogastroduodenoscopy with biopsies from the distal duodenum and proximal jejunum were unremarkable. The diarrhea and FTT persisted. A rectosigmoidoscopy with biopsies was performed; the results led to the diagnosis of EC at 5 months of age. Oral prednisolone 1 mg/kg/day was prescribed; however, 3 months into the treatment, persistent bloody diarrhea and FTT were still noted. Montelukast and ketotifen were added, after which diarrhea and weight gain started to improve. Prednisolone and montelukast/ketotifen were tapered off 6 months after. He remains symptom free and has normal growth and development in a 5-year follow-up. |
format | Online Article Text |
id | pubmed-8077466 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-80774662021-05-10 Successful Montelukast Treatment in an Infant with Steroid-Resistant Eosinophilic Colitis Wang, Nai-Wei Hsieh, Hsuan Yang, Yao-Jong Case Rep Gastroenterol Single Case Eosinophilic colitis (EC) belongs to a group of idiopathic diseases called eosinophilic gastrointestinal disorders, which are characterized by eosinophil-predominant inflammation in the gastrointestinal tract. Corticosteroids is the first-line pharmacotherapy for EC refractory to diet therapy. We report an infant with steroid-resistant EC, who successfully returned to a healthy growth trajectory under the combined therapy of montelukast and ketotifen. An 8-month-old boy presented with bloody diarrhea, anemia, and failure to thrive (FTT) that started 6 days after birth. The patient has no known allergies. A trial of elementary diet was unsuccessful. The results of several stool cultures were unremarkable. Similarly, lower gastrointestinal series failed to identify anything significant. At 3 months of age, an esophagogastroduodenoscopy with biopsies from the distal duodenum and proximal jejunum were unremarkable. The diarrhea and FTT persisted. A rectosigmoidoscopy with biopsies was performed; the results led to the diagnosis of EC at 5 months of age. Oral prednisolone 1 mg/kg/day was prescribed; however, 3 months into the treatment, persistent bloody diarrhea and FTT were still noted. Montelukast and ketotifen were added, after which diarrhea and weight gain started to improve. Prednisolone and montelukast/ketotifen were tapered off 6 months after. He remains symptom free and has normal growth and development in a 5-year follow-up. S. Karger AG 2021-03-18 /pmc/articles/PMC8077466/ /pubmed/33976616 http://dx.doi.org/10.1159/000513146 Text en Copyright © 2021 by S. Karger AG, Basel https://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 Wang, Nai-Wei Hsieh, Hsuan Yang, Yao-Jong Successful Montelukast Treatment in an Infant with Steroid-Resistant Eosinophilic Colitis |
title | Successful Montelukast Treatment in an Infant with Steroid-Resistant Eosinophilic Colitis |
title_full | Successful Montelukast Treatment in an Infant with Steroid-Resistant Eosinophilic Colitis |
title_fullStr | Successful Montelukast Treatment in an Infant with Steroid-Resistant Eosinophilic Colitis |
title_full_unstemmed | Successful Montelukast Treatment in an Infant with Steroid-Resistant Eosinophilic Colitis |
title_short | Successful Montelukast Treatment in an Infant with Steroid-Resistant Eosinophilic Colitis |
title_sort | successful montelukast treatment in an infant with steroid-resistant eosinophilic colitis |
topic | Single Case |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077466/ https://www.ncbi.nlm.nih.gov/pubmed/33976616 http://dx.doi.org/10.1159/000513146 |
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