Ovarian Cancer
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Clinical Background

Ovarian cancer is a relatively uncommon gynecologic cancer in the U.S.

Epidemiology

  • Incidence - 40/100,000 for postmenopausal females
  • Age - median age is 60 years
  • Sex - exclusively female

Risk Factors

  • Increased risk
    • Family history of breast or ovarian cancer
      • Genetic predisposition only identified in 5% of cases
      • Associated with BRCA-1, BRCA-2 and Lynch Syndrome II
      • Higher probability of BRCA mutations in Ashkenazi Jews
    • Nulliparity
  • Decreased risk is associated with:
    • Oral contraceptive use
    • Pregnancy
    • Lactation
    • History of tubal ligation

Pathophysiology

  • Malignant transformation of the epithelium of the ovarian surface
  • Often spreads early to the contiguous peritoneal mesothelium
    • Spread follows the flow of peritoneal fluid

Clinical Presentation

  • Symptoms are most often nonspecific, most patients present with stage III or IV disease
  • Abdominal symptoms
    • Abdominal fullness, dyspepsia, early satiety, bloating, pelvic pain
  • Physical findings
    • Ascites
    • Pleural effusions
    • Umbilical mass (Sister Mary Joseph nodule)
    • Ovarian mass
    • Unusual findings
      • Seborrheic keratoses (Leser-Trélat)
      • Migratory superficial thrombophlebitis (Trousseau sign)
      • Subacute cerebellar degeneration (paraneoplastic syndrome)
      • Palmar fasciitis
      • Dermatomyositis

Prevention

  • In patients with known BRCA-1 or BRCA-2 mutation who have completed childbearing, bilateral salpingo-oophorectomy dramatically reduces risk for ovarian cancer
    • Small risk of primary peritoneal serous carcinoma will still exist
See Also
  Breast Cancer Management Assays

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