Novel Ultrastructural Insights into the Clear-Cell Carcinoma of the Pancreas: A Case Report

Int J Mol Sci. 2024 Apr 13;25(8):4313. doi: 10.3390/ijms25084313.

Abstract

Pancreatic cancer, most frequently as ductal adenocarcinoma (PDAC), is the third leading cause of cancer death. Clear-cell primary adenocarcinoma of the pancreas (CCCP) is a rare, aggressive, still poorly characterized subtype of PDAC. We report here a case of a 65-year-old male presenting with pancreatic neoplasia. A histochemical examination of the tumor showed large cells with clear and abundant intracytoplasmic vacuoles. The clear-cell foamy appearance was not related to the hyperproduction of mucins. Ultrastructural characterization with transmission electron microscopy revealed the massive presence of mitochondria in the clear-cell cytoplasm. The mitochondria showed disordered cristae and various degrees of loss of structural integrity. Immunohistochemistry staining for NADH dehydrogenase [ubiquinone] 1 alpha subcomplex, 4-like 2 (NDUFA4L2) proved specifically negative for the clear-cell tumor. Our ultrastructural and molecular data indicate that the clear-cell nature in CCCP is linked to the accumulation of disrupted mitochondria. We propose that this may impact on the origin and progression of this PDAC subtype.

Keywords: clear-cell primary adenocarcinoma; extracellular vesicles; mitochondria; pancreas; transmission electron microscopy.

Publication types

  • Case Reports

MeSH terms

  • Adenocarcinoma, Clear Cell / metabolism
  • Adenocarcinoma, Clear Cell / pathology
  • Adenocarcinoma, Clear Cell / ultrastructure
  • Aged
  • Carcinoma, Pancreatic Ductal / metabolism
  • Carcinoma, Pancreatic Ductal / pathology
  • Carcinoma, Pancreatic Ductal / ultrastructure
  • Humans
  • Immunohistochemistry
  • Male
  • Microscopy, Electron, Transmission
  • Mitochondria* / metabolism
  • Mitochondria* / pathology
  • Mitochondria* / ultrastructure
  • Pancreatic Neoplasms* / metabolism
  • Pancreatic Neoplasms* / pathology
  • Pancreatic Neoplasms* / ultrastructure

Grants and funding

This research was performed thanks to the PhD grant in Translational Medicine awarded to V.G. and to the Italian Ministry of University and Research (MUR) funds (ex 60%) provided to R.D.P. and S.A.