| Literature DB >> 31084520 |
Maria L Beery1, Laura M Jacobsen2, Mark A Atkinson1,2, Alexandra E Butler3, Martha Campbell-Thompson1.
Abstract
Histopathology based studies of the pancreas obtained from organ donors are increasing our awareness of islet phenotypic heterogeneity during development and aging, as well as in settings of type 1 diabetes, type 2 diabetes, monogenic diabetes or other forms of this metabolic disease. Islet amyloidosis represents a histopathological feature classically ascribed to patients with type 2 diabetes. Herein, the occurrence of islet amyloidosis and its severity are reported in a child with type 1 diabetes along with histological comparisons of islet amyloidosis in two young adults with recent-onset type 1 diabetes. Islet amyloidosis was infrequent yet widely distributed throughout the pancreas in the child with type 1 diabetes and both adults with type 1 diabetes, with no such pathology seen in matched control donors. Analysis of these cases add to the increasing appreciation of islet heterogeneity in children and young adults with type 1 diabetes. Such knowledge also supports a notion that multiple pathophysiological mechanisms underlie the loss of functional β-cell mass in the spectrum of clinical phenotypes in patients with type 1 diabetes.Entities:
Keywords: Histopathology; amylin; heterogeneity; insulitis; islet amyloid polypeptide; pancreas
Mesh:
Year: 2019 PMID: 31084520 PMCID: PMC6548483 DOI: 10.1080/19382014.2019.1599707
Source DB: PubMed Journal: Islets ISSN: 1938-2014 Impact factor: 2.694