Pancreatic hemi-agenesis in MEN1: A clinical report

Eur J Med Genet. 2018 Apr;61(4):181-184. doi: 10.1016/j.ejmg.2017.11.013. Epub 2017 Nov 23.

Abstract

We first describe a patient with multiple endocrine neoplasia type 1 (MEN1) and dorsal pancreatic hemi-agenesis. Previously, pancreas divisum has been reported in MEN1. Recent data in mice have elucidated the molecular mechanisms of pancreatic endoderm specification. Disinhibition of hedgehog signaling appears to be important in how Gata4 and Gata6 variants cause pancreatic agenesis. Disinhibition of hedgehog signaling has also been observed in Men1 knockout pancreatic islets. Although we cannot exclude a spurious association between dorsal pancreatic hemi-agenesis and MEN1 in our patient, we argue that developmental abnormalities of the pancreas may have to be considered as possibly related to the MEN1 phenotype.

Keywords: Developmental gene expression regulation; Digestive system abnormalities; Multiple endocrine neoplasia type 1; Pancreas.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Female
  • Humans
  • Multiple Endocrine Neoplasia Type 1 / diagnostic imaging
  • Multiple Endocrine Neoplasia Type 1 / genetics*
  • Multiple Endocrine Neoplasia Type 1 / pathology
  • Mutation
  • Pancreas / abnormalities*
  • Pedigree
  • Phenotype
  • Proto-Oncogene Proteins / genetics*

Substances

  • MEN1 protein, human
  • Proto-Oncogene Proteins