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Severe Refractory Coeliac Disease with Response Only to Parenteral Nutrition
Refractory coeliac disease (RCD) is characterised by recurrent or persistent malabsorptive symptoms and villous atrophy, despite strict adherence to a gluten-free diet for at least 6 months and where other causes of malabsorption including malignancy have been excluded. There is limited evidence and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241638/ https://www.ncbi.nlm.nih.gov/pubmed/25473387 http://dx.doi.org/10.1159/000368394 |
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author | Ng, Ka Ying Bonnie Mehta, Ravi Mohamed, Salma Mohamed, Zameer Arnold, Jayantha |
author_facet | Ng, Ka Ying Bonnie Mehta, Ravi Mohamed, Salma Mohamed, Zameer Arnold, Jayantha |
author_sort | Ng, Ka Ying Bonnie |
collection | PubMed |
description | Refractory coeliac disease (RCD) is characterised by recurrent or persistent malabsorptive symptoms and villous atrophy, despite strict adherence to a gluten-free diet for at least 6 months and where other causes of malabsorption including malignancy have been excluded. There is limited evidence and guidance on the effective management of these patients. We describe a case of severe RCD in our hospital, with symptoms controlled effectively only by total parenteral nutrition (TPN). This 68-year-old woman initially presented to the clinic with persistent non-bloody diarrhoea and vomiting. A diagnosis of coeliac disease was confirmed with a positive tissue transglutaminase assay and histology. A strict gluten-free diet was ineffective and she represented 6 months later with 13 kg weight loss (16.7%), ongoing abdominal pain and diarrhoea, with bowels opening 16 times a day. She was oedematous, had an albumin of 12 g/l and required hospital admission. She was treated for pancreatic insufficiency and presumptively for small bowel bacterial overgrowth with no resolution of symptoms. We ruled out infectious causes and investigated for small bowel malignancy; all results were negative. Small bowel enteroscopy showed ulcerative jejunitis. She was given 5 days of TPN, following which her symptoms improved and albumin normalised. This was sustained with symptom resolution and weight gain seen at follow-up. TPN successfully and rapidly induced remission in this case. Thus, a short period of TPN should be considered as a potential component of management in patients with severe RCD. |
format | Online Article Text |
id | pubmed-4241638 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-42416382014-12-03 Severe Refractory Coeliac Disease with Response Only to Parenteral Nutrition Ng, Ka Ying Bonnie Mehta, Ravi Mohamed, Salma Mohamed, Zameer Arnold, Jayantha Case Rep Gastroenterol Published online: October, 2014 Refractory coeliac disease (RCD) is characterised by recurrent or persistent malabsorptive symptoms and villous atrophy, despite strict adherence to a gluten-free diet for at least 6 months and where other causes of malabsorption including malignancy have been excluded. There is limited evidence and guidance on the effective management of these patients. We describe a case of severe RCD in our hospital, with symptoms controlled effectively only by total parenteral nutrition (TPN). This 68-year-old woman initially presented to the clinic with persistent non-bloody diarrhoea and vomiting. A diagnosis of coeliac disease was confirmed with a positive tissue transglutaminase assay and histology. A strict gluten-free diet was ineffective and she represented 6 months later with 13 kg weight loss (16.7%), ongoing abdominal pain and diarrhoea, with bowels opening 16 times a day. She was oedematous, had an albumin of 12 g/l and required hospital admission. She was treated for pancreatic insufficiency and presumptively for small bowel bacterial overgrowth with no resolution of symptoms. We ruled out infectious causes and investigated for small bowel malignancy; all results were negative. Small bowel enteroscopy showed ulcerative jejunitis. She was given 5 days of TPN, following which her symptoms improved and albumin normalised. This was sustained with symptom resolution and weight gain seen at follow-up. TPN successfully and rapidly induced remission in this case. Thus, a short period of TPN should be considered as a potential component of management in patients with severe RCD. S. Karger AG 2014-10-07 /pmc/articles/PMC4241638/ /pubmed/25473387 http://dx.doi.org/10.1159/000368394 Text en Copyright © 2014 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article licensed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported license (CC BY-NC) (www.karger.com/OA-license), applicable to the online version of the article only. Users may download, print and share this work on the Internet for noncommercial purposes only, provided the original work is properly cited, and a link to the original work on http://www.karger.com and the terms of this license are included in any shared versions. |
spellingShingle | Published online: October, 2014 Ng, Ka Ying Bonnie Mehta, Ravi Mohamed, Salma Mohamed, Zameer Arnold, Jayantha Severe Refractory Coeliac Disease with Response Only to Parenteral Nutrition |
title | Severe Refractory Coeliac Disease with Response Only to Parenteral Nutrition |
title_full | Severe Refractory Coeliac Disease with Response Only to Parenteral Nutrition |
title_fullStr | Severe Refractory Coeliac Disease with Response Only to Parenteral Nutrition |
title_full_unstemmed | Severe Refractory Coeliac Disease with Response Only to Parenteral Nutrition |
title_short | Severe Refractory Coeliac Disease with Response Only to Parenteral Nutrition |
title_sort | severe refractory coeliac disease with response only to parenteral nutrition |
topic | Published online: October, 2014 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241638/ https://www.ncbi.nlm.nih.gov/pubmed/25473387 http://dx.doi.org/10.1159/000368394 |
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