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Severe spruelike enteropathy and collagenous colitis caused by olmesartan
BACKGROUND: Olmesartan, which is an angiotensin II receptor blocker, reportedly causes spruelike enteropathy, with intestinal villous atrophy as its typical histopathological finding. Interestingly, collagenous and/or lymphocytic gastritis and colitis occur in some patients. We report the case of a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461977/ https://www.ncbi.nlm.nih.gov/pubmed/34556042 http://dx.doi.org/10.1186/s12876-021-01926-y |
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author | Kaneko, Shiho Matsuda, Kana Mizuta, Yasuko Shiratori, Shoya Kishi, Kazuma Nakamura, Akihisa Yagisawa, Masataka Ehira, Nobuyuki Uebayashi, Minoru Kobayashi, Hiroya |
author_facet | Kaneko, Shiho Matsuda, Kana Mizuta, Yasuko Shiratori, Shoya Kishi, Kazuma Nakamura, Akihisa Yagisawa, Masataka Ehira, Nobuyuki Uebayashi, Minoru Kobayashi, Hiroya |
author_sort | Kaneko, Shiho |
collection | PubMed |
description | BACKGROUND: Olmesartan, which is an angiotensin II receptor blocker, reportedly causes spruelike enteropathy, with intestinal villous atrophy as its typical histopathological finding. Interestingly, collagenous and/or lymphocytic gastritis and colitis occur in some patients. We report the case of a 73-year-old Japanese man with a 2-month clinical history of severe diarrhea and weight loss. There were few reports in which spruelike enteropathy and collagenous colitis were both observed and could be followed up. CASE PRESENTATION: We report a case of a 73-year-old man with a 2-month clinical history of severe diarrhea and weight loss. He had taken olmesartan for hypertension treatment for 5 years. Endoscopic examination with biopsies revealed intestinal villous atrophy and collagenous colitis. Suspecting enteropathy caused by olmesartan, which was discontinued on admission because of hypotension, we continued to stop the drug. Within 3 weeks after olmesartan discontinuation, his clinical symptoms improved. After 3 months, follow-up endoscopy showed improvement of villous atrophy but not of the thickened collagen band of the colon. However, the mucosa normalized after 6 months, histologically confirming that the preexistent pathology was finally resolved. CONCLUSIONS: This report presents a case in which spruelike enteropathy and collagenous colitis were both observed and could be followed up. In unexplained cases of diarrhea, medication history should be reconfirmed and this disease should be considered a differential diagnosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12876-021-01926-y. |
format | Online Article Text |
id | pubmed-8461977 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-84619772021-09-24 Severe spruelike enteropathy and collagenous colitis caused by olmesartan Kaneko, Shiho Matsuda, Kana Mizuta, Yasuko Shiratori, Shoya Kishi, Kazuma Nakamura, Akihisa Yagisawa, Masataka Ehira, Nobuyuki Uebayashi, Minoru Kobayashi, Hiroya BMC Gastroenterol Case Report BACKGROUND: Olmesartan, which is an angiotensin II receptor blocker, reportedly causes spruelike enteropathy, with intestinal villous atrophy as its typical histopathological finding. Interestingly, collagenous and/or lymphocytic gastritis and colitis occur in some patients. We report the case of a 73-year-old Japanese man with a 2-month clinical history of severe diarrhea and weight loss. There were few reports in which spruelike enteropathy and collagenous colitis were both observed and could be followed up. CASE PRESENTATION: We report a case of a 73-year-old man with a 2-month clinical history of severe diarrhea and weight loss. He had taken olmesartan for hypertension treatment for 5 years. Endoscopic examination with biopsies revealed intestinal villous atrophy and collagenous colitis. Suspecting enteropathy caused by olmesartan, which was discontinued on admission because of hypotension, we continued to stop the drug. Within 3 weeks after olmesartan discontinuation, his clinical symptoms improved. After 3 months, follow-up endoscopy showed improvement of villous atrophy but not of the thickened collagen band of the colon. However, the mucosa normalized after 6 months, histologically confirming that the preexistent pathology was finally resolved. CONCLUSIONS: This report presents a case in which spruelike enteropathy and collagenous colitis were both observed and could be followed up. In unexplained cases of diarrhea, medication history should be reconfirmed and this disease should be considered a differential diagnosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12876-021-01926-y. BioMed Central 2021-09-23 /pmc/articles/PMC8461977/ /pubmed/34556042 http://dx.doi.org/10.1186/s12876-021-01926-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Kaneko, Shiho Matsuda, Kana Mizuta, Yasuko Shiratori, Shoya Kishi, Kazuma Nakamura, Akihisa Yagisawa, Masataka Ehira, Nobuyuki Uebayashi, Minoru Kobayashi, Hiroya Severe spruelike enteropathy and collagenous colitis caused by olmesartan |
title | Severe spruelike enteropathy and collagenous colitis caused by olmesartan |
title_full | Severe spruelike enteropathy and collagenous colitis caused by olmesartan |
title_fullStr | Severe spruelike enteropathy and collagenous colitis caused by olmesartan |
title_full_unstemmed | Severe spruelike enteropathy and collagenous colitis caused by olmesartan |
title_short | Severe spruelike enteropathy and collagenous colitis caused by olmesartan |
title_sort | severe spruelike enteropathy and collagenous colitis caused by olmesartan |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461977/ https://www.ncbi.nlm.nih.gov/pubmed/34556042 http://dx.doi.org/10.1186/s12876-021-01926-y |
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