Ovarian-type stroma in hepatobiliary cystadenomas and pancreatic mucinous cystic neoplasms: an immunohistochemical study

Am J Clin Pathol. 2008 Feb;129(2):211-8. doi: 10.1309/U2BBP4EMBAHCM6E6.

Abstract

We compared immunohistochemical expression of hepatocyte growth factor (HGF), c-met, alpha-inhibin, estrogen receptor (ER), and progesterone receptor (PR) in 10 pancreatic mucinous cystic neoplasms (PMCNs), 8 hepatobiliary cystadenomas (HBCs), and 6 simple liver cysts (SLCs).All HBCs and PMCNs were in women (mean ages, 45.7 and 54.9 years, respectively; P > .05). All HBCs had abundant stroma; PMCN stromal density was more variable (score, 3.0 vs 1.8; P < .05). Stroma in HBCs had greater ER and PR staining (both P < .05) and more consistent, focal, strong reactivity for alpha-inhibin than PMCNs (P < .05). SLCs were found in men and women, lacked ovarian-type stroma, and were negative for ER, PR, and alpha-inhibin. HGF expression was not significantly different in the epithelium of HBCs, PMCNs, and SLCs; c-met expression in the epithelium of HBCs and PMCNs was significantly stronger than in SLCs (P < .05). Differences in stromal density and ER, PR, and alpha-inhibin immunoreactivity in HBCs and PMCNs suggest that different hormonal environments in the liver and pancreas contribute to stromal variation. Up-regulation of c-met in HBCs and PMCNs suggests c-met activation in the pathogenesis of pancreaticobiliary cystic neoplasms.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Bile Duct Neoplasms / metabolism*
  • Bile Duct Neoplasms / pathology*
  • Cystadenoma / metabolism*
  • Cystadenoma / pathology*
  • Cystadenoma, Mucinous / metabolism*
  • Cystadenoma, Mucinous / pathology*
  • Cysts / metabolism
  • Cysts / pathology
  • Female
  • Hepatocyte Growth Factor / analysis
  • Humans
  • Immunohistochemistry
  • Inhibins / analysis
  • Liver Diseases / metabolism
  • Liver Diseases / pathology
  • Male
  • Middle Aged
  • Ovary / pathology
  • Pancreatic Neoplasms / metabolism*
  • Pancreatic Neoplasms / pathology*
  • Proto-Oncogene Proteins c-met / analysis
  • Receptors, Estrogen / analysis
  • Receptors, Progesterone / analysis
  • Stromal Cells / pathology

Substances

  • Receptors, Estrogen
  • Receptors, Progesterone
  • inhibin-alpha subunit
  • Inhibins
  • Hepatocyte Growth Factor
  • Proto-Oncogene Proteins c-met