Inflammatory Bowel Disease Following Allogeneic Hematopoietic Cell Transplant for Sickle Cell Disease.
Document Type
Article
Publication Date
1-2026
Abstract
Although graft-versus-host disease (GvHD) is an important cause of gastrointestinal (GI) complications after allogeneic hematopoietic stem cell transplantation (HCT), the non-specific symptoms make diagnosis challenging. We described three patients with sickle cell disease who developed inflammatory bowel disease (IBD) like manifestations 4-18 months post-HCT. All patients received peripheral blood stem cell grafts and sirolimus for GvHD prophylaxis. All had chronic diarrhea, and biopsies showed extensive colonic ulceration, non-necrotizing granulomas, with minimal histologic evidence of GvHD. Symptoms resolved promptly with IBD-directed therapy. Our report highlights the importance of considering alternative rare etiologies for GI complications such as IBD after HCT.
Publication Title
Pediatric blood & cancer
Volume
73
Issue
1
First Page
32121
Last Page
32121
Recommended Citation
Rowland, E., Sharma, A., Paglinco, S., Maltz, R., Deyo, J., Joglekar, K., Alberty, J., Fitzhugh, C., & Rangarajan, H. (2026). Inflammatory Bowel Disease Following Allogeneic Hematopoietic Cell Transplant for Sickle Cell Disease.. Pediatric blood & cancer, 73 (1), 32121-32121. https://doi.org/https://doi.org/10.1002/pbc.32121