S5173 Rare Presentation of CMV Jejunitis Masquerading as Crohn’s Disease: A Case Report

Introduction: Cytomegalovirus (CMV) is a dsDNA virus belonging to the Herpesviridae family. While CMV infection is typically asymptomatic in immunocompetent individuals, it can cause significant morbidity and mortality in immunocompromised individuals. We report a rare case of CMV jejunitis in a kidney transplant recipient presenting with chronic diarrhea and small bowel obstruction (SBO), mimicking Crohn’s Disease on imaging and endoscopy. Case Description/Methods: Forty-six-year-old man with history of ESRD status post deceased donor kidney transplant on mycophenolate, belatacept, and tacrolimus presented with worsening abdominal pain and diarrhea for 6 months. Symptoms persisted after discontinuation of mycophenolate. Initial imaging and serum CMV polymerase chain reaction (PCR) testing were unremarkable. Repeat computed tomography of abdomen and pelvis (CTAP) revealed distal SBO and mesenteric lymphadenopathy, normal esophagogastroduodenoscopy and colonoscopy with negative biopsies, and elevated fecal calprotectin 467 µg/g, concerning for inflammatory bowel disease (IBD). Magnetic resonance enterography revealed 8 cm segmental distal ileitis. Crohn’s Disease was suspected. He was readmitted with worsening symptoms. CTAP demonstrated partial SBO with a transition point in the jejunum and small bowel Enteroscopy revealed severe ulceration and stenosis in the mid jejunum, associated with a large amount of food that could not pass. Biopsies were obtained. Crohn’s Disease remained the leading differential, and the patient was empirically started on prednisone while awaiting histology. Surprisingly, biopsy showed Active CMV with inclusion bodies appearing within infected cells. Prednisone was discontinued, intravenous ganciclovir was initiated for 10 days, followed by a prolonged oral course. The patient’s symptoms resolved and he was discharged. Discussion: CMV enteritis is exceedingly rare and presents a diagnostic challenge because the non-specific clinical presentation overlaps with a variety of conditions, including IBD, drug-induced enteritis, and bacterial or parasitic infections. Radiologic and endoscopic findings may mimic Crohn’s Disease, including mucosal ulceration, strictures, and mesenteric lymphadenopathy. Negative blood CMV PCR, as seen in this case, is common in isolated gastrointestinal involvement and should not exclude CMV from the differential. Misdiagnosis may result in inappropriate treatment, such as immunosuppressive corticosteroids, which can exacerbate viral infection and worsen outcomes.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001148152.41013.11
Primary Topic
Cytomegalovirus and herpesvirus research
Type
article
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article

S5173 Rare Presentation of CMV Jejunitis Masquerading as Crohn’s Disease: A Case Report

Seth Richter, Justin Bilello, Mohsin Chundrigar, Stephen Hasak et al.
The American Journal of Gastroenterology
Cytomegalovirus and herpesvirus research
article

S5173 Rare Presentation of CMV Jejunitis Masquerading as Crohn’s Disease: A Case Report

Seth Richter, Justin Bilello, Mohsin Chundrigar, Stephen Hasak, Eckardt Jensen, Rabbia Irfan, Shamayel Safdar
article en

Abstract

Introduction: Cytomegalovirus (CMV) is a dsDNA virus belonging to the Herpesviridae family. While CMV infection is typically asymptomatic in immunocompetent individuals, it can cause significant morbidity and mortality in immunocompromised individuals. We report a rare case of CMV jejunitis in a kidney transplant recipient presenting with chronic diarrhea and small bowel obstruction (SBO), mimicking Crohn’s Disease on imaging and endoscopy. Case Description/Methods: Forty-six-year-old man with history of ESRD status post deceased donor kidney transplant on mycophenolate, belatacept, and tacrolimus presented with worsening abdominal pain and diarrhea for 6 months. Symptoms persisted after discontinuation of mycophenolate. Initial imaging and serum CMV polymerase chain reaction (PCR) testing were unremarkable. Repeat computed tomography of abdomen and pelvis (CTAP) revealed distal SBO and mesenteric lymphadenopathy, normal esophagogastroduodenoscopy and colonoscopy with negative biopsies, and elevated fecal calprotectin 467 µg/g, concerning for inflammatory bowel disease (IBD). Magnetic resonance enterography revealed 8 cm segmental distal ileitis. Crohn’s Disease was suspected. He was readmitted with worsening symptoms. CTAP demonstrated partial SBO with a transition point in the jejunum and small bowel Enteroscopy revealed severe ulceration and stenosis in the mid jejunum, associated with a large amount of food that could not pass. Biopsies were obtained. Crohn’s Disease remained the leading differential, and the patient was empirically started on prednisone while awaiting histology. Surprisingly, biopsy showed Active CMV with inclusion bodies appearing within infected cells. Prednisone was discontinued, intravenous ganciclovir was initiated for 10 days, followed by a prolonged oral course. The patient’s symptoms resolved and he was discharged. Discussion: CMV enteritis is exceedingly rare and presents a diagnostic challenge because the non-specific clinical presentation overlaps with a variety of conditions, including IBD, drug-induced enteritis, and bacterial or parasitic infections. Radiologic and endoscopic findings may mimic Crohn’s Disease, including mucosal ulceration, strictures, and mesenteric lymphadenopathy. Negative blood CMV PCR, as seen in this case, is common in isolated gastrointestinal involvement and should not exclude CMV from the differential. Misdiagnosis may result in inappropriate treatment, such as immunosuppressive corticosteroids, which can exacerbate viral infection and worsen outcomes.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 49%
Cytomegalovirus and herpesvirus research
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