Olmesartan-Associated Enteropathy With Severe Diarrhoea and Acute Kidney Injury

Olmesartan-associated enteropathy (OAE) is a rare but clinically significant adverse reaction to the angiotensin II receptor blocker (ARB) olmesartan. Clinically and histologically, it can mimic celiac disease but is typically reversible after drug discontinuation. We report the case of a 53-year-old man who presented with profuse watery diarrhea, dehydration, and acute kidney injury requiring hospitalization. An extensive diagnostic evaluation, including imaging studies, serological testing, and microbiologic assays, was negative. Duodenal biopsies demonstrated villous blunting with marked intraepithelial lymphocytosis. After discontinuation of olmesartan, gastrointestinal symptoms resolved completely, and renal function normalized within two weeks. Notably, an unintentional rechallenge with olmesartan led to rapid symptom recurrence, strongly supporting the diagnosis. This case highlights the need for a high clinical suspicion of OAE in patients with unexplained chronic diarrhea on olmesartan therapy. Early recognition is essential for recovery and helps avoid unnecessary invasive investigations and complications.

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Publication Details

Journal
Cureus
Published
2026-03-08
DOI
https://doi.org/10.7759/cureus.104862
Primary Topic
Celiac Disease Research and Management
Type
article
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article

Olmesartan-Associated Enteropathy With Severe Diarrhoea and Acute Kidney Injury

Arina Nikolaeva, Andrea Della Vecchia
Cureus
Celiac Disease Research and Management
article

Olmesartan-Associated Enteropathy With Severe Diarrhoea and Acute Kidney Injury

Arina Nikolaeva, Andrea Della Vecchia
article en

Abstract

Olmesartan-associated enteropathy (OAE) is a rare but clinically significant adverse reaction to the angiotensin II receptor blocker (ARB) olmesartan. Clinically and histologically, it can mimic celiac disease but is typically reversible after drug discontinuation. We report the case of a 53-year-old man who presented with profuse watery diarrhea, dehydration, and acute kidney injury requiring hospitalization. An extensive diagnostic evaluation, including imaging studies, serological testing, and microbiologic assays, was negative. Duodenal biopsies demonstrated villous blunting with marked intraepithelial lymphocytosis. After discontinuation of olmesartan, gastrointestinal symptoms resolved completely, and renal function normalized within two weeks. Notably, an unintentional rechallenge with olmesartan led to rapid symptom recurrence, strongly supporting the diagnosis. This case highlights the need for a high clinical suspicion of OAE in patients with unexplained chronic diarrhea on olmesartan therapy. Early recognition is essential for recovery and helps avoid unnecessary invasive investigations and complications.

Cureus
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Celiac Disease Research and Management
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