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Published byDina Kennedy Modified over 6 years ago
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Associated professor of Ob& Gyn fellowship of Gynecology oncology
Molar Pregnancy GTD T Allameh MD Associated professor of Ob& Gyn fellowship of Gynecology oncology
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GTD Complete hydatidiform mole Partial hydatidiform mole
Benign & premalignant
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Gestational Ttophoblastic neoplasia (GTN)
Invasive mole Choriocarcinoma Placental site trophoblastic tumor Epithelioid trophoblastic tumor
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Hydatidiform mole Originate in villous trophoblast
Abnormal chorionic villi Trophoblastic hyperplasia Overexpression of paternal genes
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Complete hydatidiform mole
80% homozygous 46XX( duplication of single sperm following fertilization of an ovum in which the maternal chromosomes are lost) 20% 46XX or 46 XY (dispermic fertilization ) Rarely biparental , autosomal recessive condition ( recurrent HMS, ovum donation )
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Partial hydatidiform mole
Triploid (fertilization of an normal ovum by two sperm 69XXX or 69XXY or 69 XYY) Presence of a fetus Amniotic fluid is present Placenta in enlarged and cystic Increased transverse diameter of gestational sac Theca lutein cyst are usually absent hCG levels of generally lower than complete mole
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Epidemiology North American & European countries /100,000 pregnancy Latin American ,Asian and Middle East / 100,000 pregnancy
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Risk factors Maternal age < 15 and > 35pr Prior molar pregnancy
*After the first mole 1 to 1.5% (10 to 15 times ↑ ) *After two mole % Decreasing levels of dietary carotene
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Clinical features High hCG Vaginal bleeding Pelvic pressure or pain
Uterine size greater than gestational age Hyperemesis gravidarum Hyperthyroidism Ovarian theca lutein cyst Preeclampsia <20 weeks Anemia Passage of hydropic vesicles
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Diagnostic evaluation
History Physical examination (vagina should be examined for metastases - common sites of metastases include the vagina, lungs, liver, CNS) Pelvic ultrasound (snow storm or Swiss cheese pattern )
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Theca lutein cysts
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Laboratory evaluation
hCG if more than 100,000 TVS should be performed – if apparently normal singleton gestation , sono and hCG should be repeated in1 week( normal fetus and co-existent molar pregnancy) Blood type and antibody screen Chest radiograph if the patient has pulmonary symptoms
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Multiple gestation Normal co-twin with a mole(1/20000 to 1/ pregnancy) Detected by pelvic sono Preeclampsia , hemorrhage , thyrotoxicosis Preterm delivery ,GTN - 57% delivered alive baby at 34 weeks - 26.7% GTN developed These patients may continue the pregnancy under careful monitoring
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Familiar recurrent molar pregnancy
Biparental molar Typically familial Related genes are at choromosoms 19q
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Management of hydatidiform mole
Surgical uterine evacuation Medical uterine evacuation Hystrectomy
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Surgical uterine evacuation
* suction curettage * Laminaria * fundal massage if uterus is larger than 14 weeks * We do not use prostaglandins for cervical ripening * starting at the time of anesthesia induction ,oxytocin infusion (10 units in1 liter ringer lactate solution at50 drops/min )
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Medical uterine evacuation
medication –only methods , misoprostol, mifepristone, oxytocin are controversial because of increase risk of trophoblastic embolization and obtaining a specimen for pathology 26% required uterine curettage 9% required chemotherapy ( 4-6% after uterine curettage)
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Hysterectomy For women with HM who are > 40 y and have completed child bearing. In one study GTN developed in 54% women treated with dilatation and evacuation and in non of the hysterectomy patients If hCG levels > (ultra high risk ) Prophylactic chemo or TAH Eliminate local invasion and reduce GTN The ovaries may be preserved ( ovarian metastases are rare ) Large theca lutein cyst can be aspirated
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Prophylactic chemotherapy
High risk women Hormonal follow up unavailable or unreliable Do not impact future fertility Methotrexate or actinomyycin D 63% reduction in the risk of GTN ( delay in diagnosis of GTN ? )
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Management of complication
Hyperthyroidism (antithyroid ) Beta adrenal blocking agent may be required before the induction of anesthesia Ovarian theca lutein cyst ( regress over 2-4 months, may need aspiration ) Preeclampsia (resolves promptly after molar evacuation ) Cardiopulmonary symptoms ( resolve within 72h after evacuation)
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Follow up Serial hCG *Every week until non detectable for 3 weeks ,then *Every month for 6 months *Trying to become pregnant
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Shorter duration of monitoring
Allow patients to become pregnant after achieving 3 consecutive weekly Followed by 3 consecutive monthly undetectable hCG level
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Diagnosis of GTN hCG levels plateau ( remain within + percent of the previous result) Over a 3 weeks period( days 1,7, 14 and 21) hCG level increases > 10% over a 2 weeks duration(days 1,7 and 14) Persistence of detectable hCG for more than 6 months after molar evacuation
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Persistent low hCG(quiescent GTN)
Will fail to normalize and remain elevated at low levels ( <200 at least 3months) Absence of any clinical or radiological evidence of GTN May develop after partial mole , invasive mole or choricarcinoma Small focus of highly differentiated non invasive syncytiotrophoblast
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Quiescent GTN Foci of disease are not readily identifiable clinically
hCG level is unresponsive to therapy The measurement of hyper glycosylated hCG ( hCG-H) has been proposed in patients with quiescent GTN. hCG- H is produced by cytotrophoblast and is associated with trophoblast invasion growth of cytotrophoblast cells and promotion of placental implantation hCG- H is a promoter of choriocarcinoma ,tumorigenesis and is the main form of hCG produced in active GTN
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hCG - H Low level indicate quiescent GTN
Increasing levels indicate the development of active GTN that requires GTN Patients with quiescent GTN should be monitored with monthly hCG and avoid pregnancy Active GTN should be diagnosed and treated If hCG –H rises to greater than 20 % of total hCG or if total hCG has 2 doublings
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Contraception Hormonal contraception Barrier methods
IUD should not be used before the hCG normalizes (uterine perforation )
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Gestational trophoblastic neoplasia GTN
Complete mole (15-20 %) Partial mole (1-5 %)
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Risk factors for GTN Complete mole with signs of trophoblastic proliferation ( uterine size greater than gestational age , hCG> ) Ovarian theca lutein cysts > 6 cm Age >35-40 y
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Subsequent pregnancy Patients with MH can anticipate normal reproductive outcomes Repeat molar pregnancy * After 1 molar pregnancy % * After 2 molar pregnancy %
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Obstetric management First trimester ultrasound to confirm normal pregnancy Measurement of hCG at 6 weeks after the completion of pregnancy ( term or abortion) , to exclude choriocarcinoma Placenta should be examined and sent to pathology Product of conception from abortions should be examined pathologically
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