| Literature DB >> 25765064 |
M D Bellin1,2, A Moran1, J J Wilhelm2, T D O'Brien3, P A Gottlieb4, L Yu4, T B Dunn5.
Abstract
Total pancreatectomy with islet autotransplantation (TPIAT) is performed for definitive treatment of chronic pancreatitis; patients are not diabetic before surgery, or have C-peptide positive pancreatogenous diabetes. Thus, TPIAT recipients are not traditionally considered at risk for autoimmune loss of the islet graft. We describe a 43-year-old female who underwent TPIAT with high mass islet graft of 6031 IEQ/kg, with no evidence of presurgical β cell autoimmunity who developed type 1 diabetes within the first year after TPIAT, resulting in complete loss of beta cell function. The patient had positive GAD and insulin autoantibodies at 1 year and 18 months after TPIAT, not present prior, and undetectable C-peptide after mixed meal and intravenous glucose tolerance testing at 18 months. Glucagon secretion was preserved, suggesting the transplanted alpha cell mass was intact. HLA typing revealed a DR3/DR4 class II haplotype. This case highlights the need to consider de novo type 1 diabetes in patients with unexpected islet graft failure after TPIAT. © Copyright 2015 The American Society of Transplantation and the American Society of Transplant Surgeons.Entities:
Keywords: autoimmunity; autotransplantation; diabetes: type 1; insulin / C-peptide; islets of Langerhans
Mesh:
Year: 2015 PMID: 25765064 DOI: 10.1111/ajt.13216
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086