S6185 When the Gut Doesn’t Forget: Recurrent Eosinophilic Gastroenteritis Following COVID-19 Infection

Introduction: Eosinophilic gastroenteritis (EGE) is a rare inflammatory disorder of the stomach and small intestine, characterized by dense eosinophilic infiltration in the absence of secondary causes (e.g., parasitic infection, malignancy, or systemic eosinophilic syndrome). Its prevalence in the United States is approximately 5.1 per 100,000. Case Description/Methods: A 28-year-old man presented with a 3-day history of profuse, watery diarrhea and lower abdominal pain. He reported 3 similar episodes over the past 4 years, the first occurring weeks after a hospitalization for coronavirus disease 2019 (COVID-19). He denied food intolerances, atopic disorders, or significant environmental exposures. Laboratory tests showed WBC 15.1 × 10³/µL (16% eosinophils), and elevated CRP (1.6 mg/dL) and stool calprotectin (53 µg/g). Celiac and parasitic studies, ANCA panel, ASCA titers, serum tryptase and IgE levels, and cultures were unremarkable. Computed tomography showed diffuse gastritis and enterocolitis with skip lesions, suggesting inflammatory bowel disease (IBD). Esophagogastroduodenoscopy showed normal esophagus and stomach but moderate, diffuse edema and erythema in the duodenum. Colonoscopy showed a grossly normal terminal ileum and colon. Duodenal biopsies revealed preserved villi with a marked eosinophilic infiltration (>100/HPF) in the lamina propria and submucosa, without lymphocytosis, celiac changes, dysplasia, or malignancy. Gastric biopsies showed 15-20 eosinophils/HPF, and a random ascending colon biopsy revealed reactive lymphoid aggregates with focal eosinophilia. Collectively, these findings supported the diagnosis of EGE. The patient received intravenous methylprednisolone for 2 days with rapid resolution of diarrhea and eosinophilia. He was discharged on a 4-week prednisone taper with GI follow-up. Discussion: Recent evidence shows that COVID-19 can trigger eosinophilic gastrointestinal disorders (EGIDs) like EGE, by disrupting gut immunity and causing a type 2 helper T-cell response that recruits eosinophils into the intestinal lining. Multiple case reports document EGE onset within weeks of acute COVID-19, even in patients without a history of atopy. In these cases, symptoms and imaging often resemble IBD, but targeted biopsies reveal eosinophilic infiltration essential for an accurate diagnosis. As post-COVID-19 EGE becomes increasingly recognized, clinicians should consider EGIDs in any patient with recent SARS-CoV-2 infection who presents with diarrhea and abdominal pain, especially when imaging suggests IBD but endoscopic mucosa appears deceptively normal.

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001153200.71525.79
Primary Topic
Eosinophilic Esophagitis
Type
article
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article

S6185 When the Gut Doesn’t Forget: Recurrent Eosinophilic Gastroenteritis Following COVID-19 Infection

The American Journal of Gastroenterology
Eosinophilic Esophagitis
article

S6185 When the Gut Doesn’t Forget: Recurrent Eosinophilic Gastroenteritis Following COVID-19 Infection

article en

Abstract

Introduction: Eosinophilic gastroenteritis (EGE) is a rare inflammatory disorder of the stomach and small intestine, characterized by dense eosinophilic infiltration in the absence of secondary causes (e.g., parasitic infection, malignancy, or systemic eosinophilic syndrome). Its prevalence in the United States is approximately 5.1 per 100,000. Case Description/Methods: A 28-year-old man presented with a 3-day history of profuse, watery diarrhea and lower abdominal pain. He reported 3 similar episodes over the past 4 years, the first occurring weeks after a hospitalization for coronavirus disease 2019 (COVID-19). He denied food intolerances, atopic disorders, or significant environmental exposures. Laboratory tests showed WBC 15.1 × 10³/µL (16% eosinophils), and elevated CRP (1.6 mg/dL) and stool calprotectin (53 µg/g). Celiac and parasitic studies, ANCA panel, ASCA titers, serum tryptase and IgE levels, and cultures were unremarkable. Computed tomography showed diffuse gastritis and enterocolitis with skip lesions, suggesting inflammatory bowel disease (IBD). Esophagogastroduodenoscopy showed normal esophagus and stomach but moderate, diffuse edema and erythema in the duodenum. Colonoscopy showed a grossly normal terminal ileum and colon. Duodenal biopsies revealed preserved villi with a marked eosinophilic infiltration (>100/HPF) in the lamina propria and submucosa, without lymphocytosis, celiac changes, dysplasia, or malignancy. Gastric biopsies showed 15-20 eosinophils/HPF, and a random ascending colon biopsy revealed reactive lymphoid aggregates with focal eosinophilia. Collectively, these findings supported the diagnosis of EGE. The patient received intravenous methylprednisolone for 2 days with rapid resolution of diarrhea and eosinophilia. He was discharged on a 4-week prednisone taper with GI follow-up. Discussion: Recent evidence shows that COVID-19 can trigger eosinophilic gastrointestinal disorders (EGIDs) like EGE, by disrupting gut immunity and causing a type 2 helper T-cell response that recruits eosinophils into the intestinal lining. Multiple case reports document EGE onset within weeks of acute COVID-19, even in patients without a history of atopy. In these cases, symptoms and imaging often resemble IBD, but targeted biopsies reveal eosinophilic infiltration essential for an accurate diagnosis. As post-COVID-19 EGE becomes increasingly recognized, clinicians should consider EGIDs in any patient with recent SARS-CoV-2 infection who presents with diarrhea and abdominal pain, especially when imaging suggests IBD but endoscopic mucosa appears deceptively normal.

The American Journal of GastroenterologyVol. 120(10S2)
Good health and well-being
Openalex Percentile: Top 29%
Eosinophilic Esophagitis
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