Management of reproductive health in Cowden syndrome complicated by endometrial polyps and breast cancer

Obstet Gynecol. 2013 Feb;121(2 Pt 2 Suppl 1):461-464.

Abstract

Background: Cowden syndrome is an autosomal-dominant condition associated with mutations in the tumor suppressor gene PTEN. Gynecologic malignancies are common with a 5-10% risk of endometrial cancer and 25-50% risk of breast cancer.

Case: A 37-year-old woman with a history of breast cancer, other neoplasms, and multiple skin lesions was diagnosed with Cowden syndrome after a germline PTEN mutation was identified. The endometrium had high glucose uptake on positron emission tomography scan and was irregularly thickened on ultrasonography; biopsy revealed endometrial polyps and simple hyperplasia. Fifteen months later, hysteroscopy again confirmed numerous benign endometrial polyps.

Conclusion: Recurrent, multiple endometrial polyps portend a high risk of endometrial cancer in women with Cowden syndrome. Monitoring for malignancy and consideration of hysterectomy after childbearing is completed is warranted.

Trial registration: ClinicalTrials.gov NCT00971789.

Publication types

  • Case Reports
  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Breast Neoplasms / genetics
  • Breast Neoplasms / surgery*
  • Endometrial Neoplasms / diagnosis
  • Endometrial Neoplasms / genetics
  • Endometrial Neoplasms / surgery*
  • Female
  • Fertility Preservation
  • Hamartoma Syndrome, Multiple / genetics
  • Hamartoma Syndrome, Multiple / surgery*
  • Hodgkin Disease / complications
  • Humans
  • PTEN Phosphohydrolase / genetics
  • Polyps / diagnosis
  • Polyps / genetics
  • Polyps / surgery*
  • Thyroid Neoplasms / genetics
  • Thyroid Neoplasms / surgery

Substances

  • PTEN Phosphohydrolase
  • PTEN protein, human

Associated data

  • ClinicalTrials.gov/NCT00971789