S5152 A Wormy Surprise: Unmasking Strongyloides in Eosinophilic Colitis

Introduction: Eosinophilic colitis (EoC) is defined as abnormal infiltration of eosinophilic polymorphonuclear cells in the colonic mucosa. Although common in children under 2 years old, it is rare in adults. EoC is classified as primary and secondary, which is crucial for guiding management. We present a rare case of secondary EoC. Case Description/Methods: A 61-year-old man with a history of severe allergies, GERD, and eosinophilic esophagitis was referred by an allergist for oral irritation triggered by various foods. EGD revealed Barrett’s esophagus, as well as erythematous mucosa in the gastric body, antrum, and duodenum. Biopsies confirmed eosinophilic esophagitis (>15 eosinophils per high-power field) and were negative for CD117 immunostaining for clustering mast cells. Colonoscopy revealed multiple 1 mm white lesions in the cecum, ascending, and transverse colon (TC), 11 tubular adenomas (<5 mm), and 1 sessile serrated lesion with a necrotizing granuloma in the TC. Biopsies throughout the colon revealed background mucosa with marked, patchy mucosal eosinophilia ranging between 150 and >400 eosinophils per HPF. CD117 immunostaining was negative for clustering mast cells. Biopsies of the terminal ileum showed increased lamina propria inflammation. MRI enterography was negative for acute or chronic gastroenteritis. An infectious workup was positive for Strongyloides IgG antibody, likely the primary culprit of his colonoscopy findings and peripheral eosinophilia. The patient was started on omeprazole 40 mg twice a day indefinitely and ivermectin. Repeat procedures showed resolution of his infectious colitis. Discussion: Although not standardized, one proposed criterion for EoC is >40 eosinophils/HPF in at least 2 colonic segments. Primary EoC is a diagnosis of exclusion, whereas secondary EoC has many etiologies. Parasitic infections account for 5 to 10% of cases, most commonly including Strongyloides, pinworms, toxocariasis, schistosomiasis, etc. The diagnostic sensitivity of parasitic infections is poor, hence the need for repeated stool and serological tests. The most common findings on colonoscopy are minute, raised lesions, which are collections of eosinophils surrounding a dead Strongyloides larva (Splendore-Hoeppli phenomenon). These lesions may enlarge and become necrotic (possibly explaining the TC polyp), resulting in ulcerations. Treatment involves anti-helminthic agents rather than immunosuppressants for primary EoC. This case highlights a rare form of EoC due to Strongyloides.

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001148068.90215.63
Primary Topic
Eosinophilic Esophagitis
Type
article
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article

S5152 A Wormy Surprise: Unmasking Strongyloides in Eosinophilic Colitis

The American Journal of Gastroenterology
Eosinophilic Esophagitis
article

S5152 A Wormy Surprise: Unmasking Strongyloides in Eosinophilic Colitis

article en

Abstract

Introduction: Eosinophilic colitis (EoC) is defined as abnormal infiltration of eosinophilic polymorphonuclear cells in the colonic mucosa. Although common in children under 2 years old, it is rare in adults. EoC is classified as primary and secondary, which is crucial for guiding management. We present a rare case of secondary EoC. Case Description/Methods: A 61-year-old man with a history of severe allergies, GERD, and eosinophilic esophagitis was referred by an allergist for oral irritation triggered by various foods. EGD revealed Barrett’s esophagus, as well as erythematous mucosa in the gastric body, antrum, and duodenum. Biopsies confirmed eosinophilic esophagitis (>15 eosinophils per high-power field) and were negative for CD117 immunostaining for clustering mast cells. Colonoscopy revealed multiple 1 mm white lesions in the cecum, ascending, and transverse colon (TC), 11 tubular adenomas (<5 mm), and 1 sessile serrated lesion with a necrotizing granuloma in the TC. Biopsies throughout the colon revealed background mucosa with marked, patchy mucosal eosinophilia ranging between 150 and >400 eosinophils per HPF. CD117 immunostaining was negative for clustering mast cells. Biopsies of the terminal ileum showed increased lamina propria inflammation. MRI enterography was negative for acute or chronic gastroenteritis. An infectious workup was positive for Strongyloides IgG antibody, likely the primary culprit of his colonoscopy findings and peripheral eosinophilia. The patient was started on omeprazole 40 mg twice a day indefinitely and ivermectin. Repeat procedures showed resolution of his infectious colitis. Discussion: Although not standardized, one proposed criterion for EoC is >40 eosinophils/HPF in at least 2 colonic segments. Primary EoC is a diagnosis of exclusion, whereas secondary EoC has many etiologies. Parasitic infections account for 5 to 10% of cases, most commonly including Strongyloides, pinworms, toxocariasis, schistosomiasis, etc. The diagnostic sensitivity of parasitic infections is poor, hence the need for repeated stool and serological tests. The most common findings on colonoscopy are minute, raised lesions, which are collections of eosinophils surrounding a dead Strongyloides larva (Splendore-Hoeppli phenomenon). These lesions may enlarge and become necrotic (possibly explaining the TC polyp), resulting in ulcerations. Treatment involves anti-helminthic agents rather than immunosuppressants for primary EoC. This case highlights a rare form of EoC due to Strongyloides.

The American Journal of GastroenterologyVol. 120(10S2)
Reduced inequalities
Openalex Percentile: Top 29%
Eosinophilic Esophagitis
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