S5132 A Diagnostic Dilemma: Fulminant EBV Colitis Masquerading as Ulcerative Colitis

Introduction: Epstein-Barr virus (EBV) infection with gastrointestinal (GI) tract involvement is rare. Its clinical and histological features can mimic other etiologies. Here, we present a case of a 31-year-old man, initially suspected to have inflammatory bowel disease (IBD), later confirmed to have EBV colitis. Case Description/Methods: A 31-year-old man with congenital HIV infection and poor compliance to antiretroviral therapy (ART) presented with abdominal pain, hematochezia and unintentional weight loss for the past 2 months. Physical exam revealed diffuse abdominal tenderness. Laboratory tests showed leukocytosis, microcytic anemia, a CD4 count of 54 cells/uL, and an HIV viral load of 637,000 copies/mL. Polymerase chain reaction (PCR) stool studies for common bacteria and viruses were negative. Colonoscopy showed mucosal erythema and loss of vascular markings. Mesalamine and steroids were started, but his symptoms worsened and abdominal computed tomography (CT) showed severe pancolitis with diffuse colonic distention. Repeat colonoscopy for decompression tube placement showed severely punched out, ulcerated mucosa. After decompression, his symptoms improved briefly before he developed intractable vomiting. Repeat CT revealed pneumoperitoneum. Emergent exploratory laparotomy showed toxic colitis with transverse colon perforation, requiring a total abdominal colectomy with end ileostomy. Pathological examination revealed neutrophilic infiltrate in the lamina propria and mild-moderate chronic inflammatory infiltrate without crypt architectural distortion or crypt abscesses. EBV RNA was by in situ hybridization. Next-generation-sequencing and PCR of colonic tissue showed normal GI flora. The patient had an uneventful post-operative course with symptom resolution. He was discharged on ART with infectious diseases outpatient follow up. Discussion: EBV is often implicated in self-limiting mononucleosis. It can also be associated with GI lymphoma, but involvement in the tract without overt lymphoma is rare, with only a few cases reported in the literature. GI-tract EBV infections can present as diarrhea, hematochezia, and abdominal pain, resembling IBD. However, fulminant colitis resulting in perforation and colectomy is highly unusual. Dense inflammatory infiltrates in the lamina propria and positive immunohistochemical staining differentiate it from other causes. It is crucial to consider EBV when evaluating severe colitis of unknown origin, especially in the setting of immune compromise, like in our patient.

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001147988.64780.7b
Primary Topic
Diagnosis and treatment of tuberculosis
Type
article
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article

S5132 A Diagnostic Dilemma: Fulminant EBV Colitis Masquerading as Ulcerative Colitis

The American Journal of Gastroenterology
Diagnosis and treatment of tuberculosis
article

S5132 A Diagnostic Dilemma: Fulminant EBV Colitis Masquerading as Ulcerative Colitis

article en

Abstract

Introduction: Epstein-Barr virus (EBV) infection with gastrointestinal (GI) tract involvement is rare. Its clinical and histological features can mimic other etiologies. Here, we present a case of a 31-year-old man, initially suspected to have inflammatory bowel disease (IBD), later confirmed to have EBV colitis. Case Description/Methods: A 31-year-old man with congenital HIV infection and poor compliance to antiretroviral therapy (ART) presented with abdominal pain, hematochezia and unintentional weight loss for the past 2 months. Physical exam revealed diffuse abdominal tenderness. Laboratory tests showed leukocytosis, microcytic anemia, a CD4 count of 54 cells/uL, and an HIV viral load of 637,000 copies/mL. Polymerase chain reaction (PCR) stool studies for common bacteria and viruses were negative. Colonoscopy showed mucosal erythema and loss of vascular markings. Mesalamine and steroids were started, but his symptoms worsened and abdominal computed tomography (CT) showed severe pancolitis with diffuse colonic distention. Repeat colonoscopy for decompression tube placement showed severely punched out, ulcerated mucosa. After decompression, his symptoms improved briefly before he developed intractable vomiting. Repeat CT revealed pneumoperitoneum. Emergent exploratory laparotomy showed toxic colitis with transverse colon perforation, requiring a total abdominal colectomy with end ileostomy. Pathological examination revealed neutrophilic infiltrate in the lamina propria and mild-moderate chronic inflammatory infiltrate without crypt architectural distortion or crypt abscesses. EBV RNA was by in situ hybridization. Next-generation-sequencing and PCR of colonic tissue showed normal GI flora. The patient had an uneventful post-operative course with symptom resolution. He was discharged on ART with infectious diseases outpatient follow up. Discussion: EBV is often implicated in self-limiting mononucleosis. It can also be associated with GI lymphoma, but involvement in the tract without overt lymphoma is rare, with only a few cases reported in the literature. GI-tract EBV infections can present as diarrhea, hematochezia, and abdominal pain, resembling IBD. However, fulminant colitis resulting in perforation and colectomy is highly unusual. Dense inflammatory infiltrates in the lamina propria and positive immunohistochemical staining differentiate it from other causes. It is crucial to consider EBV when evaluating severe colitis of unknown origin, especially in the setting of immune compromise, like in our patient.

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