Origin and pathogenesis of pelvic (Ovarian, Tubal, and Primary Peritoneal) serous carcinoma

Niloofar N. Nik*, Russell Vang, Ie Ming Shih, Robert J. Kurman

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

136 Scopus citations

Abstract

A new paradigm for the pathogenesis of female pelvic cancer helps explain persistent problems in describing the development and diverse morphology of these neoplasms. This paradigm incorporates recent advances in the molecular pathogenesis of epithelial ovarian cancer (EOC) with new insights into the origin of these tumors. Correlated clinicopathologic and molecular genetic studies gave rise to a dualistic model that divides the various histologic types of EOCs into two broad categories designated type I and type II. Because serous carcinomas are the most common EOC and account for the vast majority of deaths, they form the subject of this review. Recent studies indicate that the precursor of ovarian high-grade serous carcinoma appears to develop from an occult intraepithelial carcinoma in the fimbria of the fallopian tube and involves the ovary secondarily. Another possible mechanism is implantation of normal fimbrial epithelium on the denuded ovarian surface at the site of rupture when ovulation occurs, causing the development of cortical inclusion cysts. The dualistic model serves as a framework for the study of ovarian cancer and can help investigators organize this complex group of neoplasms. It also facilitates the development of novel approaches to prevention, screening, and treatment of this devastating disease.

Original languageEnglish
Pages (from-to)27-45
Number of pages19
JournalAnnual Review of Pathology: Mechanisms of Disease
Volume9
DOIs
StatePublished - 2014
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2014 by Annual Reviews. All rights reserved.

Keywords

  • High-grade serous carcinoma
  • Low-grade serous carcinoma
  • Papillary tubal hyperplasia
  • Primary peritoneal serous carcinoma
  • STIC

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