KRAS oncogene mutations suggest a common histogenetic origin for pleomorphic giant cell tumor of the pancreas, osteoclastoma of the pancreas, and pancreatic duct adenocarcinoma

Hum Pathol. 1997 Jan;28(1):80-3. doi: 10.1016/s0046-8177(97)90283-5.

Abstract

Giant cell neoplasms of the pancreas are rare tumors of uncertain histogenesis. Mutation of the KRAS oncogene is common in typical pancreatic duct adenocarcinoma. We have analyzed DNA from five pancreatic tumors with giant cells for mutations in the KRAS oncogene and found alterations of the second position of codon 12 in each case (four G > A transitions and one G > C transversion). The common mutation pattern in tumors with giant cells and duct adenocarcinoma suggests a common route to malignant transformation and may indicate a shared histogenesis. We also tested 11 cases of malignant fibrous histiocytoma, a histological mimic of pleomorphic giant cell tumor, for mutations in the KRAS oncogene. The absence of KAS mutations in each of the malignant fibrous histiocytomas (MFHs) and in other histologically similar tumors may provide assistance in the differential diagnosis of pleomorphic pancreatic tumors.

MeSH terms

  • Adenocarcinoma / genetics*
  • Adenocarcinoma / pathology
  • Aged
  • Female
  • Genes, ras / genetics*
  • Giant Cell Tumor of Bone / genetics*
  • Giant Cell Tumor of Bone / pathology
  • Giant Cell Tumors / genetics*
  • Giant Cell Tumors / pathology
  • Humans
  • Male
  • Middle Aged
  • Mutation
  • Pancreatic Ducts* / pathology
  • Pancreatic Neoplasms / genetics*
  • Pancreatic Neoplasms / pathology