Best Practice & Research Clinical Obstetrics & Gynaecology
Volume 16, Issue 4 , Pages 499-512, August 2002

Pathology of borderline (low malignant potential) ovarian tumours

  • Jeffrey D Seidman, MD (Director of Gynecological Pathology)

      Affiliations

    • Department of Pathology, Washington Hospital Center, Washington, DC, USA
  • ,
  • Brigitte M Ronnett, MD (Associate Professor of Pathology, The Johns Hopkins, University School of Medicine and Pathologist, The Johns Hopkins Hospital, Baltimore, MD)

      Affiliations

    • Departments of Pathology and Obstetrics and Gynecology, Johns Hopkins University School of Medicine, Baltimore, MD, USA
  • ,
  • Robert J Kurman, MD (Richard W. Te Linde Distinguished Professor of Gynecologic Pathology, Departments of Gynecology, Obstetrics and Pathology)

      Affiliations

    • Departments of Pathology and Obstetrics and Gynecology, Johns Hopkins University School of Medicine, Baltimore, MD, USA

Abstract 

Recent studies suggest that the borderline group of ovarian tumours can be subclassified into benign and malignant neoplasms. The survival for patients with serous borderline tumours confined to the ovaries is virtually 100%. Patients with serous borderline tumours with invasive peritoneal implants, and with micropapillary serous carcinomas (a distinctive neoplasm previously included in the borderline category), have a 30–40% mortality rate and therefore these tumours are classified as carcinomas. After these neoplasms are excluded, the remaining advanced stage serous borderline tumours (those with non-invasive implants) have a survival rate of nearly 100% and should be considered benign. Similarly, nearly all mucinous borderline tumours reported to display aggressive behaviour have been associated with pseudomyxoma peritonei, a condition now known to be of appendiceal origin. The remaining mucinous borderline tumours are always confined to the ovaries and have a benign behaviour. Since borderline tumours can now be classified into benign and malignant types, the category has no further utility.

Keywords: ovarian neoplasms, borderline tumour, tumour of low malignant potential, ovarian carcinoma

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  • f1 Address correspondence to: Dr Jeffrey Seidman, Department of Pathology, Washington Hospital Center, 110 Irving St. N.W., Washington DC 20010, USA, or to Drs Ronnett and Kurman: Department of Pathology, Johns Hopkins Medical Institutions, 600 N. Wolf St., Baltimore MD 21287, USA.

PII: S1521-6934(02)90300-7

doi:10.1053/beog.2002.0300

Best Practice & Research Clinical Obstetrics & Gynaecology
Volume 16, Issue 4 , Pages 499-512, August 2002