De novo ulcerative colitis after kidney transplantation treated with infliximab.
Rikako OkiSumi HidakaAkiko SasakiShinichi TeshimaYasuhiro MochidaKatsunori MiyakeKunihiro IshiokaHidekazu MoriyaTakayasu OhtakeShuzo KobayashiPublished in: CEN case reports (2021)
Diarrhea is a common complication in kidney transplant recipients. Common causes of diarrhea include infection, side effect from medication, rejection, and malignancy. A less common but important cause of diarrhea is de novo inflammatory bowel disease (IBD). This is unexpected, as these patients are already immunosuppressed. Herein, we present the case of a 45-year-old man with end-stage kidney disease because of focal segmental glomerulosclerosis who underwent preemptive kidney transplantation, with his mother as donor. His immunosuppressive regimen included methylprednisolone, mycophenolate mofetil, and tacrolimus. He had no episodes of graft dysfunction, rejection, or infectious events. Two and a half years post-transplantation, he developed bloody diarrhea. After excluding infections, colonoscopy was performed and revealed edematous mucosa and erythema with pigmentation, which are typical findings in ulcerative colitis. Despite therapy with 5-aminosalicylate and granulocyte monocyte apheresis, he presented with massive bloody diarrhea. We initiated infliximab, an anti-tumor necrosis factor-α (TNF-α) agent. He responded very well and achieved remission within 6 months after initiation of infliximab, while administration of the other immunosuppressants was maintained. His course was uneventful and no complications developed. Management of immunosuppressants for de novo IBD after organ transplantation is complicated, because treatment of IBD, graft function protection, and prevention of infection must be considered. Therefore, cooperation between transplantation physicians and gastroenterologists is essential during therapy.
Keyphrases
- ulcerative colitis
- irritable bowel syndrome
- clostridium difficile
- kidney transplantation
- rheumatoid arthritis
- cell therapy
- newly diagnosed
- end stage renal disease
- ejection fraction
- primary care
- peripheral blood
- healthcare
- risk factors
- stem cells
- oxidative stress
- high dose
- prognostic factors
- single cell
- replacement therapy
- systemic lupus erythematosus
- low dose
- drug induced
- adverse drug
- combination therapy