[Ovarian carcinoma. Do the subtypes reflect different diseases?]

Pathologe. 2008 Nov:29 Suppl 2:160-2. doi: 10.1007/s00292-008-1028-9.
[Article in German]

Abstract

Lack of therapeutic options and poor reproducibility of histopathological subtypes have been the reasons that ovarian carcinomas are currently treated as monolithic entity. Histopathological grading is used to identify those patients who can be spared adjuvant therapy. With slight modifications of the WHO based subtype classification we have shown that subtypes (i.e. serous, endometrioid, clear cell, mucinous) can be reproducibly used to stratify patients according to disease-specific survival. As these pathologically identifiable subtypes have different epidemiologic and genetic risk factors, precursor lesions, molecular abnormalities and clinical behaviour, screening and management strategies have to be subtype-specific.

Publication types

  • English Abstract

MeSH terms

  • Adenocarcinoma, Clear Cell / classification
  • Adenocarcinoma, Clear Cell / genetics
  • Adenocarcinoma, Clear Cell / pathology
  • Adenocarcinoma, Mucinous / classification
  • Adenocarcinoma, Mucinous / genetics
  • Adenocarcinoma, Mucinous / pathology
  • Carcinoma, Endometrioid / classification
  • Carcinoma, Endometrioid / genetics
  • Carcinoma, Endometrioid / pathology
  • Cystadenocarcinoma, Serous / classification
  • Cystadenocarcinoma, Serous / genetics
  • Cystadenocarcinoma, Serous / pathology
  • DNA Mutational Analysis
  • Diagnosis, Differential
  • Female
  • Genetic Markers / genetics
  • Humans
  • Observer Variation
  • Ovarian Neoplasms / classification*
  • Ovarian Neoplasms / genetics
  • Ovarian Neoplasms / pathology*
  • Ovary / pathology
  • Practice Guidelines as Topic
  • Prognosis
  • Tumor Suppressor Protein p53 / genetics

Substances

  • Genetic Markers
  • TP53 protein, human
  • Tumor Suppressor Protein p53