Hürthle cell tumours of the thyroid. A review with emphasis on mitochondrial abnormalities with clinical relevance

Virchows Arch. 2000 Aug;437(2):107-15. doi: 10.1007/s004280000219.

Abstract

The molecular and enzymatic abnormalities of mitochondria in oxyphilic / oncocytic / Hürthle cells and their respective tumours are reviewed in a series of sections: "Mitochondria, ageing, neurodegenerative diseases and cancer", "Mitochondrial abnormalities in Hürthle cells and Hürthle cells tumours", "Mitochondrion-related alterations in tumours with and without Hürthle cell/oncocytic features", "True and secondary oxyphilia", and "Bcl-2 expression, apoptosis and necrosis in Hürthle cell tumours and tumour-like lesions". The clinicopathological and pathogenetic meaning of the data on record on these topics are discussed, with an emphasis on thyroid pathology.

Publication types

  • Review

MeSH terms

  • Adenoma, Oxyphilic / genetics*
  • Adenoma, Oxyphilic / metabolism*
  • DNA, Mitochondrial / genetics
  • Humans
  • Mitochondria / genetics*
  • Mutation
  • Thyroid Neoplasms / genetics*
  • Thyroid Neoplasms / metabolism*

Substances

  • DNA, Mitochondrial