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Endometrial cancer and postmenopausal bleeding

Every postmenopausal bleed is endometrial cancer until proven otherwise; transvaginal ultrasound with an endometrium of 4 mm or less is reassuring, while a thicker endometrium or recurrent bleeding requires a biopsy.

Why it matters in the exam

This is the most common gynaecological cancer in the Western world, and in the exam it appears mainly through the question "a 60-year-old woman with vaginal bleeding — what is the next step". The answer is transvaginal ultrasound or an endometrial biopsy (Pipelle), and if the biopsy is non-diagnostic or bleeding continues — hysteroscopy. Further questions deal with the risk factors, all linked to oestrogen unopposed by progesterone: obesity, nulliparity, early menarche and late menopause, polycystic ovary syndrome, tamoxifen, and oestrogen-secreting ovarian tumours (granulosa cell).

Know the difference between the endometrioid type (hormonal, common, good prognosis) and the serous type (older women, unrelated to oestrogen, aggressive), and the newer molecular classification (POLE, mismatch-repair deficiency, abnormal p53) that changes treatment. Lynch syndrome is the main hereditary cause, so mismatch-repair proteins are tested in every tumour. The basic treatment is surgery: hysterectomy and removal of the ovaries with sentinel node sampling. Hyperplasia without atypia is treated with a progestin, and atypical hyperplasia with hysterectomy, unless the woman wishes to preserve fertility.

Key points

Summary table

SituationFindingTreatmentExam notes
Postmenopausal bleedingEndometrium 4 mm or less on transvaginal ultrasoundSurveillance; biopsy if bleeding recursVery high negative predictive value
Thick endometriumAbove 4 mmBiopsy (Pipelle); non-diagnostic → hysteroscopy and curettageOn tamoxifen the endometrium is thick anyway — decide by bleeding
Hyperplasia without atypiaLow cancer riskProgestin, preferably a hormonal IUD (LNG-IUD)Follow-up biopsies
Atypical hyperplasia (EIN)Up to about 40% with coexisting cancerHysterectomy; for fertility preservation — high-dose progestin and close follow-upA precancerous lesion
Stage I-IIConfined to the uterine body (I) or the cervical stroma (II)Hysterectomy, removal of the ovaries and sentinel node; radiotherapy by riskIA: less than 50% myometrial invasion
Stage III-IVSerosa, ovaries, vagina or nodes (III); bladder, bowel or distant spread (IV)Surgery and debulking, chemotherapy and radiotherapyThe serous type spreads early to the peritoneum

A free exam question

מה מאפיין את התקלה הגנטית ב- SYNDROME LYNCH? (the question as examined, in Hebrew)

  1. א. AR מוטאציה אוטוזומאלית רצסיבית
  2. ב. MMR GENES DNA -מקבץ של מוטאציות ב
  3. ג. מוטאציה הגורמת לחוסר יציבות בגנים מקבוצת ה- .CHECK
  4. ד. MSH3 MSH5. -מוטאציות ב

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Sources

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Reviewed by the Examqo AI Professor · 2026-11-02. The text may contain errors; when in doubt, check the source.