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neo_uterine

uterine cancer

risk factors

  • overall risk for all women is 3%
  • genetic:
    • FH increases risk
      • hereditary nonpolyposis colon cancer (HNPCC or Lynch syndrome) have 70% chance of endometrial cancer
        • most cases are caused by a defect in either the mismatch repair gene MLH1 or the gene MSH2
        • at least 5 other genes can cause HNPCC: MLH3, MSH6, TGBR2, PMS1, and PMS2.
    • mutations of the ARID1A and PIK3CA genes are frequently found together in the development of endometrial cancer, as well as in endometriosis-associated ovarian cancer
      • ARID1A is a tumor suppressor. When it mutates, chromatin, cellular material that keeps DNA compacted in cells, loses its structure, allowing cancer to spread.
      • PIK3CA is an instructional gene that tells the body to produce certain proteins and leads to uncontrolled growth of cells when it mutates.
      • these same mutations often are found in women who have endometriosis but many of those affected never develop endometrial cancer suggesting additional factors are required to develop cancer
  • obesity
  • advancing age
  • oestrogen-related issues:
    • unopposed oestrogen therapy in menopause without progestogen (but taking combined increases risk of VTE and breast cancer)
    • anti-oestrogens in menopause can cause endometrial hyperplasia and increase risk to 1% per annum
    • combined oral contraceptive pill (OCP) reduces risk for 10 yrs after ceasing
    • higher number of menstrual cycles over a lifetime increases risk
      • early menarche before age 12yrs increases risk
      • late menopause increases risk
    • pregnancy reduces risk
      • 3 pregnancies reduces risk by 50% compared to no pregnancies 1)
    • certain ovarian tumours such as granulosa cell tumor which secretes high levels of oestrogen
  • iucd seems to lower risk
  • diet - high fat diets are thought to be associated with increased risk
  • lack of exercise
  • type 2 diabetes appears to double risk but obesity and lack of exercise are confounding factors
  • endometrial hyperplasia
    • Simple atypical hyperplasia becomes cancer in 8% if untreated
    • Complex atypical hyperplasia (CAH) becomes cancer in 29% if untreated
  • pelvic radiotherapy

Ix for possible malignancy

  • suspicious clinical pictures include:
    • any post-menopausal bleeding
    • clinically suggestive lesions such as cervical lesions, pelvic masses, enlarged uterus (although this may just be uterine fibroids (leiomyomas) or adenomyosis)
    • intermenstrual bleeding
    • post-coital bleeding
    • endometrial hyperplasia - eg. the perimenopausal patient with a preceding period of amenorrhoea, or those on oestrogen only Rx.
  • indications for uterine sampling3):
    • women over 45 years age
    • women with BMI > 30
    • women with FH bowel cancer
    • women with irregular bleeding
    • abnormal endometrium on US
    • NB. the chances of any endometrial pathology being present in a slim woman under age 45 years with regular menses is very small.
  • indications of hysteroscopy4):
    • suspected focal uterine pathology on US
    • suboptimal US visualisation of the endometrium
    • abnormal cavity seen on US
    • no endometrial sample can be obtained through pipelle biopsy

Post Rx care

  • short term vaginal oestrogen therapy < 2yrs appears to be safe for young endometrial cancer survivors5)
neo_uterine.txt · Last modified: 2026/03/04 21:29 by gary1

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