Fatal ulcerative enteritis of the small intestine in a patient with ulcerative colitis treated with vedolizumab

Author:

Monasterio Carmen1,Schmitt-Gräff Annette2,Pohl Matthias3,Truschel Thomas4,Warnatz Klaus5,Kreisel Wolfgang1,Thimme Robert1,Hasselblatt Peter1

Affiliation:

1. Dept. of Medicine II, Medical Center – University of Freiburg, Faculty of Medicine, University of Freiburg, Germany

2. Institute of Pathology, Medical Center – University of Freiburg, Faculty of Medicine, University of Freiburg, Germany

3. Endopraxis Markgräflerland, Müllheim, Germany

4. Helios Klinik Müllheim, Müllheim, Germany

5. Center for Chronic Immunodeficiency, Medical Center – University of Freiburg, Faculty of Medicine, University of Freiburg, Germany

Abstract

AbstractVedolizumab (VDZ) inhibits α4β7 integrins and is used to target intestinal immune responses in patients with inflammatory bowel disease, which is considered to be relatively safe. Here we report on a fatal complication following VDZ administration. A 64-year-old female patient with ulcerative colitis (UC) refractory to tumor necrosis factor inhibitors was treated with VDZ. One week after the second VDZ infusion, she was admitted to hospital with severe diarrhea and systemic inflammatory response syndrome (SIRS). Blood stream infections were ruled out, and endoscopy revealed extensive ulcerations of the small intestine covered with pseudomembranes, reminiscent of invasive candidiasis or mesenteric ischemia. Histology confirmed subtotal destruction of small intestinal epithelia and colonization with Candida. Moreover, small mesenteric vessels were occluded by hyaline thrombi, likely as a result of SIRS, while perfusion of large mesenteric vessels was not compromised. Beta-D-glucan concentrations were highly elevated, and antimycotic therapy was initiated for suspected invasive candidiasis but did not result in any clinical benefit. Given the non-responsiveness to anti-infective therapies, an autoimmune phenomenon was suspected and immunosuppressive therapy was escalated. However, the patient eventually died from multi-organ failure. This case should raise the awareness for rare but severe complications related to immunosuppressive therapy, particularly in high risk patients.

Publisher

Georg Thieme Verlag KG

Subject

Gastroenterology

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