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Cytomegalovirus Colitis in a Patient with Severe Treatment Refractory Ulcerative Colitis
Michelle M Bao1, Juliana M Kennedy1, Michael T Dolinger1
1Division of Pediatric Gastroenterology, Susan and Leonard Feinstein Inflammatory Bowel Disease Center, Icahn School of Medicine at Mount Sinai, NY, USA.
Cytomegalovirus (CMV) colitis can occur in ulcerative colitis (UC) patients, even those on advanced therapies like upadacitinib. Prompt evaluation for CMV is crucial in UC patients with worsening symptoms unresponsive to treatment.
Area of Science:
- Gastroenterology
- Infectious Diseases
- Immunology
Background:
- Cytomegalovirus (CMV) reactivation is known in ulcerative colitis (UC), but its precise role in disease progression remains unclear.
- Risk factors for CMV reactivation in UC include disease severity and immunosuppressive therapies such as corticosteroids and immunomodulators.
Purpose of the Study:
- To report a case of cytomegalovirus colitis in a pediatric patient with refractory ulcerative colitis.
- To discuss the potential role of upadacitinib in CMV reactivation within the context of UC.
Main Methods:
- Case report of a 13-year-old male with UC refractory to multiple treatments.
- Diagnosis of cytomegalovirus colitis confirmed via flexible sigmoidoscopy biopsy.
- Treatment involved intravenous ganciclovir and immunosuppression tapering, followed by surgical intervention.
Main Results:
- The patient experienced worsening symptoms despite escalating upadacitinib and prednisone therapy.
- Cytomegalovirus colitis was diagnosed and treated with ganciclovir.
- Despite initial response, the patient ultimately required subtotal colectomy and restorative proctocolectomy.
Conclusions:
- Upadacitinib, a Janus kinase inhibitor, may potentially contribute to CMV reactivation due to its effects on herpesviruses.
- CMV colitis should be considered in all ulcerative colitis patients presenting with acute symptom exacerbation, especially when refractory to current therapies.
- Diagnostic evaluation for CMV is essential in UC patients with worsening symptoms and lack of response to increased immunosuppression.
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