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Importance of duodenal bulb biopsies in children for diagnosis of celiac disease in clinical practice
BACKGROUND: The patchy nature of villous lesion in celiac disease is increasingly being recognized. Current guidelines recommend four endoscopic duodenal mucosal biopsies from the second or more distal part of the duodenum to confirm the diagnosis of celiac disease. The purpose of the study was to i...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2771033/ https://www.ncbi.nlm.nih.gov/pubmed/19835611 http://dx.doi.org/10.1186/1471-230X-9-78 |
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author | Rashid, Mohsin MacDonald, Andrea |
author_facet | Rashid, Mohsin MacDonald, Andrea |
author_sort | Rashid, Mohsin |
collection | PubMed |
description | BACKGROUND: The patchy nature of villous lesion in celiac disease is increasingly being recognized. Current guidelines recommend four endoscopic duodenal mucosal biopsies from the second or more distal part of the duodenum to confirm the diagnosis of celiac disease. The purpose of the study was to investigate the usefulness of duodenal bulb mucosal biopsies in confirming the diagnosis of celiac disease in everyday clinical practice. METHODS: All patients with a positive tissue-transglutaminase antibody requiring biopsy-confirmation of celiac disease over a two-year period were studied. Two endoscopic biopsies were taken from the duodenal bulb and four biopsies from the second (or distal) part of the duodenum. RESULTS: Thirty-five patients were included, mean age 8.1 (± 4.7) years. Thirty-one (88.6%) patients had abnormal distal duodenal biopsies, one had Marsh type 1, one had Marsh type 2 and twenty-nine had Marsh type 3 lesion. All but two patients with abnormal distal duodenal biopsies also had abnormal bulb biopsies. Four (11.4%) patients had normal distal duodenal biopsies but abnormal bulb biopsies. Of these, one patient had Marsh type 2 and three had Marsh type 3 lesion. The distal duodenum was also grossly normal in these four patients. The histological diagnosis of celiac disease would not have been possible in these four cases with distal duodenal biopsies only. CONCLUSION: The lesion in celiac disease in children can be patchy with duodenal bulb mucosa being the only area showing histological changes. The recommendations regarding the site of biopsies should be revised to include biopsies not only from distal duodenum but also from bulb to improve the diagnostic yield. |
format | Text |
id | pubmed-2771033 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27710332009-10-31 Importance of duodenal bulb biopsies in children for diagnosis of celiac disease in clinical practice Rashid, Mohsin MacDonald, Andrea BMC Gastroenterol Research Article BACKGROUND: The patchy nature of villous lesion in celiac disease is increasingly being recognized. Current guidelines recommend four endoscopic duodenal mucosal biopsies from the second or more distal part of the duodenum to confirm the diagnosis of celiac disease. The purpose of the study was to investigate the usefulness of duodenal bulb mucosal biopsies in confirming the diagnosis of celiac disease in everyday clinical practice. METHODS: All patients with a positive tissue-transglutaminase antibody requiring biopsy-confirmation of celiac disease over a two-year period were studied. Two endoscopic biopsies were taken from the duodenal bulb and four biopsies from the second (or distal) part of the duodenum. RESULTS: Thirty-five patients were included, mean age 8.1 (± 4.7) years. Thirty-one (88.6%) patients had abnormal distal duodenal biopsies, one had Marsh type 1, one had Marsh type 2 and twenty-nine had Marsh type 3 lesion. All but two patients with abnormal distal duodenal biopsies also had abnormal bulb biopsies. Four (11.4%) patients had normal distal duodenal biopsies but abnormal bulb biopsies. Of these, one patient had Marsh type 2 and three had Marsh type 3 lesion. The distal duodenum was also grossly normal in these four patients. The histological diagnosis of celiac disease would not have been possible in these four cases with distal duodenal biopsies only. CONCLUSION: The lesion in celiac disease in children can be patchy with duodenal bulb mucosa being the only area showing histological changes. The recommendations regarding the site of biopsies should be revised to include biopsies not only from distal duodenum but also from bulb to improve the diagnostic yield. BioMed Central 2009-10-16 /pmc/articles/PMC2771033/ /pubmed/19835611 http://dx.doi.org/10.1186/1471-230X-9-78 Text en Copyright ©2009 Rashid and MacDonald; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Rashid, Mohsin MacDonald, Andrea Importance of duodenal bulb biopsies in children for diagnosis of celiac disease in clinical practice |
title | Importance of duodenal bulb biopsies in children for diagnosis of celiac disease in clinical practice |
title_full | Importance of duodenal bulb biopsies in children for diagnosis of celiac disease in clinical practice |
title_fullStr | Importance of duodenal bulb biopsies in children for diagnosis of celiac disease in clinical practice |
title_full_unstemmed | Importance of duodenal bulb biopsies in children for diagnosis of celiac disease in clinical practice |
title_short | Importance of duodenal bulb biopsies in children for diagnosis of celiac disease in clinical practice |
title_sort | importance of duodenal bulb biopsies in children for diagnosis of celiac disease in clinical practice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2771033/ https://www.ncbi.nlm.nih.gov/pubmed/19835611 http://dx.doi.org/10.1186/1471-230X-9-78 |
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