Borderline Tumors and Other Rare Epithelial Tumors of the Ovary

Teresa P. Díaz-Montes, Russell Vang, Deborah K. Armstrong, Robert E. Bristow

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Borderline ovarian tumors are distinct from invasive ovarian malignancies. They account for 15% of all epithelial ovarian cancers. On an average, the age at diagnosis is approximately 10 years younger than that of women with malignant ovarian cancer. More than 80% of women with borderline ovarian tumors present with stage I disease. Overall, the survival for women with borderline ovarian tumors, stage for stage, is also significantly better. The recommended management of clinically apparent early stage borderline ovarian tumors includes bilateral salpingo-oophorectomy with hysterectomy and surgical staging for women who have completed childbearing. For young patients with apparent early stage disease who desire fertility preservation, unilateral oophorectomy or ovarian cystectomy with a staging procedure is an acceptable alternative, although this approach may predispose the patient to a higher risk of recurrence. For advanced-stage and recurrent disease, cytoreductive surgery is the cornerstone treatment, while adjuvant chemotherapy is reserved for select cases only (e.g. unresectable disease, invasive metastatic implants, rapid growth rate with progressive symptomatology).

Original languageEnglish (US)
Title of host publicationTextbook of Uncommon Cancer, Third Edition
PublisherJohn Wiley & Sons, Ltd
Pages447-454
Number of pages8
ISBN (Print)0470012021, 9780470012024
DOIs
StatePublished - Jul 11 2006

Keywords

  • Borderline tumors
  • Carcinosarcoma
  • Clear cell
  • Endometrioid
  • Malignant mixed mesodermal tumor
  • Mucinous
  • Neoplasm
  • Ovary
  • Serous

ASJC Scopus subject areas

  • Medicine(all)

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  • Cite this

    Díaz-Montes, T. P., Vang, R., Armstrong, D. K., & Bristow, R. E. (2006). Borderline Tumors and Other Rare Epithelial Tumors of the Ovary. In Textbook of Uncommon Cancer, Third Edition (pp. 447-454). John Wiley & Sons, Ltd. https://doi.org/10.1002/0470030542.ch40