Prof Dr Esraa ALMaini 2019 2020 Endometrial hyperplasia

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Prof. Dr Esraa AL-Maini 2019 -2020 Endometrial hyperplasia

Prof. Dr Esraa AL-Maini 2019 -2020 Endometrial hyperplasia

Endometrial thickness guidelines premenopausal women : Endometrial thickness in normal endometrial vary according to

Endometrial thickness guidelines premenopausal women : Endometrial thickness in normal endometrial vary according to day of cycle ≤ 4 mm on day 4 of the menstrual cycle ≤ 8 mm by day 8.

� Persistent endometrial thickness, independent of cycle day, measuring =>12 mm should be further

� Persistent endometrial thickness, independent of cycle day, measuring =>12 mm should be further evaluated especially for women those with risk factors for endometrial carcinoma.

Etiology for endometrial hyperplasia. A-Endogenous estrogen. The most common cause Chronic anovulation is associated

Etiology for endometrial hyperplasia. A-Endogenous estrogen. The most common cause Chronic anovulation is associated with _The polycystic ovary syndrome(PCOS) _ Ovarian tumor (eg, granulosa cell tumor _ Obese women B- Exogenous estrogen.

Classification endometrial hyperplasia The World Health Organization classification of endometrial hyperplasia is based upon

Classification endometrial hyperplasia The World Health Organization classification of endometrial hyperplasia is based upon two factors: 1. Simple or complex glandular/stromal architectural pattern 2. The presence or absence of nuclear atypia

. Endometrial carcinoma is more than 10 -fold more likely in atypical hyperplasia (simple

. Endometrial carcinoma is more than 10 -fold more likely in atypical hyperplasia (simple or complex).

Risk factors 1 -Increasing age 2 -Unopposed estrogen therapy 3 -Late menopause (after age

Risk factors 1 -Increasing age 2 -Unopposed estrogen therapy 3 -Late menopause (after age 55) 4 -Nulliparity 5 -Polycystic ovary syndrome (Chronic anovulation) 6 -Obesity 7 -Diabetes 8 -Hereditary nonpolyposis colorectal cancer 9 -Tamoxifen 10 -Early menarche 11 -Estrogen secreting tumor 12 -Family history of endometrial, ovarian, breast, or colon cancer

Clinical manifestations. Endometrial hyperplasia should be suspected in: 1 - Women with heavy, prolonged,

Clinical manifestations. Endometrial hyperplasia should be suspected in: 1 - Women with heavy, prolonged, frequent (ie, less than 21 days). 2 - Irregular uterine bleeding. Abnormal uterine bleeding in perimenopausal or postmenopausal women is the most common clinical symptom of endometrial neoplasia, although such (PMB)bleeding is usually (80%) due to a benign condition.

Diagnostic and surveillance methods for endometrial hyperplesia 1 -Transvaginal sonography; may have a role

Diagnostic and surveillance methods for endometrial hyperplesia 1 -Transvaginal sonography; may have a role in diagnosing endometrial hyperplasia in pre- and postmenopausal women 2 -Endometrial biopsy : diagnosis of endometrial hyperplasia requires histological examination of the endometrial tissue. 1 -Office biopsy(out patients) 2 -D/C biopsy. 3 -Hysteroscopic guided biopsy

Indication for evaluation of the endometrium 1 -Abnormal -uterine bleeding with risk factors 2

Indication for evaluation of the endometrium 1 -Abnormal -uterine bleeding with risk factors 2 -Failure to respond to medical treatment for abnormal uterine bleeding 3 -unopposed estrogen replacement therapy 4 - Asymptomatic women presence of endometrial cells on Pap smear if they are at increased risk of endometrial cancer 5 -Women with hereditary nonpolyposis colorectal cancer

B. Indications for additional diagnostic evaluation by hysteroscopy/directed biopsy 1 -Endometrial hyperplasia with atypia

B. Indications for additional diagnostic evaluation by hysteroscopy/directed biopsy 1 -Endometrial hyperplasia with atypia by office biopsy, further evaluation by Dilation and curettage (D&C) is needed to exclude a coexistent endometrial adenocarcinoma(% 25) 2. Non diagnostic office biopsy. Endometrial hyperplasia/cancer needs to be excluded in women with a non diagnostic office biopsy. hysteroscopy/directed biopsy 3. Persistent bleeding. After benign endometrial biopsy or treatment of endometrial pathology. hysteroscopy/directed biopsy 4. Postmenopausal women. hysteroscopy/directed biopsy

Management of hyperplasia without atypia � 1 - Observation alone �The risk of progressing

Management of hyperplasia without atypia � 1 - Observation alone �The risk of progressing to endometrial cancer is less than 5% over 20 years. �The majority o will regress spontaneously during follow-up. �Observation alone with follow-up endometrial biopsies to ensure disease regression can be considerd , especially when identifiable risk factors such as obesity and the use of (HRT) can be reversed.

2 -Treatment with progestogens Higher disease regression rate than observation alone. indications: 1 -In

2 -Treatment with progestogens Higher disease regression rate than observation alone. indications: 1 -In women who fail to regress following observation alone 2 - In symptomatic women with abnormal uterine bleeding. Types of progesterone; 1 - Local progesterone ([LNG-IUS]) should be the first-line medical treatment because compared with 2: It has a higher disease regression rate More favourable bleeding profile It is associated with fewer adverse effects. 2 -Continuous oral progesterone should be used (medroxyprogesterone 10– 20 mg/day or norethisterone 10– 15 mg/day) for women who decline the LNG-IUS. Cyclical progestogens should not be used

The duration of treatment and follow-up of hyperplasia without atypia �- Treatment with oral

The duration of treatment and follow-up of hyperplasia without atypia �- Treatment with oral progestogens or the LNG-IUS should be for a minimum of 6 months in order to induce histological regression , women should be encouraged to retain the LNG-IUS for 5 YEARS this reduces the risk of relapse � 1 -If adverse effects are tolerable � 2 -fertility is not desired � 3 -If it alleviates abnormal uterine bleeding symptoms.

FOLLOW UP ; � � � -Endometrial surveillance with outpatient endometrial biopsy should be

FOLLOW UP ; � � � -Endometrial surveillance with outpatient endometrial biopsy should be arranged at a minimum of 6 -monthly intervals. -At least two consecutive 6 -monthly negative biopsies should be obtained. -Women should be advised to seek a further advice if abnormal vaginal bleeding recurs after completion of treatment because this may indicate disease relapse. In women at higher risk of relapse; -As body mass index (BMI) of 35 or greater Those treated with oral progestogens 6 -monthly and endometrial biopsies are recommended Once two consecutive negative endometrial biopsies have been obtained long-term follow-up should be considered with annual endometrial biopsies.

3 -Surgical management( Hysterectomy ) should not first-line treatment because progestogen induces remission in

3 -Surgical management( Hysterectomy ) should not first-line treatment because progestogen induces remission in the majority avoids the morbidity Hysterectomy is indicated in women not wanting to preserve their fertility when 1 -Progression to atypical hyperplasia during follow-up, 2 - No histological regression after 12 months of treatment 3 - Relapse of endometrial hyperplasia after completing progestogen 4 - Persistence of bleeding symptoms 5 -The woman declines to undergo endometrial surveillance or comply with medical treatment

Types of surgery 1 - Postmenopausal women should be offered a bilateral salpingo-oophorectomy together

Types of surgery 1 - Postmenopausal women should be offered a bilateral salpingo-oophorectomy together with the total hysterectomy. 2 - premenopausal women, the decision to remove the ovaries should be individualised; reduce the risk of a future ovarian malignancy. 3 - A laparoscopic approach is preferable. 4 - Endometrial ablation is not recommended.

Management of atypical hyperplasia 1 - Total Hysterectomy because of - The risk of

Management of atypical hyperplasia 1 - Total Hysterectomy because of - The risk of underlying malignancy 25%, Progression to cancer 25 -50% laparoscopic approach - Postmenopausal should be offered bilateral salpingo-oophorectomy - -premenopausal women, the decision to remove the ovaries individualised; but removal will reduce the risk of a future ovarian malignancy. Endometrial ablation is not recommended

� 2 --Women with atypical hyperplasia who wish to preserve their fertility or who

� 2 --Women with atypical hyperplasia who wish to preserve their fertility or who are not suitable for surgery � Women wishing to retain their fertility should be counselled about the risks � Pretreatment investigations should aim to rule out invasive endometrial cancer or co-existing ovarian cancer by TVUS and endometrial biopsy � First-line treatment with the LNG-IUS should be recommended, with oral progestogens as a secondbest alternative � Once fertility is no longer required, hysterectomy should be offered because high risk of disease relapse

� followed up �TVUS and endometrial biopsy : at 3 months interval until minimum

� followed up �TVUS and endometrial biopsy : at 3 months interval until minimum two consecutive negative biopsies are obtained So two negative and asymptomatic women long-term follow-up with endometrial biopsy every 6– 12 months is recommended until a hysterectomy is performed.

� In women wishing to conceive � Disease regression should be achieved on at

� In women wishing to conceive � Disease regression should be achieved on at least one endometrial sample before women attempt to conceive. � Assisted reproduction may be considered as the live birth rate is higher and it may prevent relapse.

�HRT and endometrial hyperplasia � 1 - Systemic estrogen-only HRT should not be used

�HRT and endometrial hyperplasia � 1 - Systemic estrogen-only HRT should not be used in women with a uterus. � 2 - All women taking HRT should be encouraged to report any unscheduled vaginal bleeding promptly. � 3 - advised to change to continuous progestogen intake using the LNG-IUS or a continuous combined HRT preparation.

Observation alone Treat with progesteron IUS –oral No atypical cell 6 m -5 years

Observation alone Treat with progesteron IUS –oral No atypical cell 6 m -5 years follow up 6 m until 2 –ve If symptoms recure or high risk so yearly biopsy Hysterectomy not 1 st line indicated if Progress , not regress , relapse , poor compliance refuse IUS

Fertility is concern exclude ovarian cancer endometrial before treatment IUS -oral progesterone 3 -month

Fertility is concern exclude ovarian cancer endometrial before treatment IUS -oral progesterone 3 -month follow up biopsy until 2 –ve atypical cell then 6 -12 month biopsy until hysterectomy Hysterectomy 1 st line with BSO in Post Menop.

THANK YOU

THANK YOU