Severe spruelike enteropathy and collagenous colitis caused by olmesartan

• Published in: BMC gastroenterology Vol. 21; no. 1; pp. 1 - 6
• Main Authors: Kaneko, Shiho, Matsuda, Kana, Mizuta, Yasuko, Shiratori, Shoya, Kishi, Kazuma, Nakamura, Akihisa, Yagisawa, Masataka, Ehira, Nobuyuki, Uebayashi, Minoru, Kobayashi, Hiroya
• Format: Journal Article
• Language: English
• Published: London BioMed Central Ltd 23.09.2021; BioMed Central; BMC
• Subjects: Angiotensin; Angiotensin II; Angiotensin II receptor blockers; Atrophy; Biopsy; Case Report; Case reports; Case studies; Causes of; Celiac disease; Colitis; Collagen; Collagenous colitis; Colon; Colonoscopy; Complications and side effects; Diarrhea; Differential diagnosis; Endoscopy; Gastritis; Gastroenterology; Hypotension; Inflammatory bowel disease; Intestinal diseases; Intestine; Mucosa; Small intestine; Spruelike enteropathy; Villous atrophy; Japan
• ISSN: 1471-230X; 1471-230X
• DOI: 10.1186/s12876-021-01926-y

Abstract 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.