12 trophoblast

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Gestational Trophoblasti c Diseases LIU Sui-ling Third Affiliated Hospital of Sun Yat-sen Univer sity [email protected]

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Gestational Trophoblastic Diseases

LIU Sui-ling

Third Affiliated Hospital of Sun Yat-sen University

[email protected]

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• Gestational Trophoblastic Diseases(GTD)– Hydatidiform mole– Invasive mole– Choriocarcinoma– Placental-site trophoblastic tumor (PSTT)

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• Features– Derived from fetal tissue– Composed of syncytiotropho-blastic and cytot

rophoblastic cell except PSTT– In PSTT, only the intermediate trophoblasts

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Ovum

conceptus

sperm

Fetus

Placenta

Fetal membrane

Amniotic fluid

Umbilical cord

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Normal villi

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HYDATIDIFORM MOLE

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Hydatidiform mole

• Incidence– Area– Economic status– Age– Diet

• Recurrent rate< 2%

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Hydatidiform mole

• Etiology– Cytogenetic study

• euploid • paternal in origin

• Pathogenesis– Homozygous conceptus with propensity for alt

ered growth

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Hydatidiform mole

• Pathology– Classic findings

• Edema of the villous stroma• Avascular villi• Nests of proliferating syncytiotrophoblastic or cytotr

ophoblastic elements surrounding villi

– Classification• Complete hydatidiform mole• partial hydatidiform mole

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Complete hydatidiform mole

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Multiple grapelike vesicles

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Microscopic findings of hydatidiform mole

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Partial hydatidiform mole

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Partial hydatidiform mole with fetus

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Microscopic findings of partial hydatidiform mole

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HYDATIDIFORM MOLE comparison of complete and partial hydatidiform mole

Complete Partial

Karyotype Diploid( 46,XX or 46,XY) Triploid(69,XXX or 69,XXY)

Embryo Absent PresentVilli Hydropic Few hydropicTrophoblasts Diffuse hyperplasia Mild focal hyperplasiaImplantation-site trophoblast Diffuse atypia Focal atypiaFetal RBCs Absent Presentβ-hCG High(> 50,000) Slight elevation(< 50,00

0)Frequency of classical clinical symptoms Common RareRisk for persistent GTT 20%-30% < 5%

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HYDATIDIFORM MOLE

• CLINICAL FINDINGS– Symptoms And Signs

• Abnormal uterine bleeding• Nausea and vomiting• Excessive uterine size for gestational date• Multiple theca lutein cysts• Pain• Preeclampsia• Hyperthyroidism

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HYDATIDIFORM MOLE

• Laboratory Findings– hCG– The amount of hCG correlates closely with the

number of viable tumor cells– β-hCG decline to normal within 14 weeks follo

wing evacuation of a molar pregnancy

• Special examinations– ultrasound

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Ultrasound pattern of hydatiform mole

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HYDATIDIFORM MOLE

• DIFFERENTIAL DIAGNOSIS– Normal pregnancy

• TREATMENT– Evacuation

• Suction curettage• Gentle sharp currettage• Oxytocin• Pathologic study• Laparotomy setup• hysterectomy

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HYDATIDIFORM MOLE

• Prophylactic chemotherapy– Controversial– Patients with complete hydatidiform mole at hi

gh risk• Age>35• History of prior molar pregnancy• Poor followup

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HYDATIDIFORM MOLE

• Surveillance following molar pregancy– Important

• The incidence of malignant disease is 20%~ 30%

– Serial β-hCG determinations• Weekly determination to nondetectable β-hCG leve

l• Monthly determination for at least 1 year

– Oral contraceptives

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Case of hydatidiform mole• 25 years old, G1P0A0, admitted to hospital at Aug.3-200

9 because of “Cessation of menstruation for 10 weeks, abnormal uterine bleeding for one week”.

• History: The LMP of the patient was May.25-2009. She was diagnosed “early pregnancy” at 6 weeks. She complained of small amount of uterine bleeding for week. Furthermore, she felt nausea and vomiting from 2 days before.

• Physical examination: T 36.5 BP 150/110mmHg (BB℃P120/70mmHg) R 20/min P 92/min. Normal signs of lung and heart. Both lower limbs had pitting edema. Gynecological conditions: Uterine fundus at the level of umbilcus. 6-cm adnexal masses were palpated at both side of uterus.

• Assistant examinations: HGB 90g/L;

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Case of hydatidiform mole

• Diagnosis

1 hydatidiform mole

2 Preeclampsia

3 Anemia

• Assistant examinationsβ-hCG ultrasound

• TREATMENTEvacuation

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MALIGNANT GESTATIONAL TROPHOBLASTIC

NEOPLASIA

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• Reference

http://www.china-obgyn.net/lecture/Index.html

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MALIGNANT GESTATIONAL TROPHOBLASTIC NEOPLASIA

• PATHOLOGY– Invasive mole

• Hydatidiform mole that invades the myometrium or adjacent structure

• Microscopic findings are the same as in hydatidiform

– Choriocarcinoma• Pure epithelial tumor composed of syncytiotropho-blastic and

cytotrophoblastic cell• Sheets or foci of trophoblasts, hemorrhage and necrosis• No villi

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Invasive mole

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Microscopic findings in invasive mole

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Uterus of choriocarcinoma

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Trophoblasts of choriocarcinoma

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MALIGNANT GESTATIONAL TROPHOBLASTIC NEOPLASIA

• DIAGNOSIS – history– Pelvic examination

• Enlarged uterus • Ovarian enlargment

– X-ray– CT– Serum hCG– Hematologic counts– Hepatic and renal function

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vaginal metastasis of choriocarcinoma

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MALIGNANT GESTATIONAL TROPHOBLASTIC NEOPLASIA

• TREATMENT – Nonmetastatic Gestational Trophoblastic Disease

• Single-agent chemotherapy– Medicine

» Methotrexate» Dactinomycin

– Course and interval– Treatment cycles– Followup

» β-hCG , blood count, liver and renal function

• Combined chemotherapy and hysterectomy

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MALIGNANT GESTATIONAL TROPHOBLASTIC NEOPLASIA

– Metastatic Gestational Trophoblastic Disease • Chemotherapy

– Single-agent– Multiple-agent

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MALIGNANT GESTATIONAL TROPHOBLASTIC NEOPLASIA

• CLINICAL CLASSIFICATION OF MALIGNANT GESTATIONAL TROPHOBLASTIC DISEASES

1. National Cancer Institute

2. World Health Organization– Low risk – Medium risk– High risk

3. Revised FIGO

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MALIGNANT GESTATIONAL TROPHOBLASTIC NEOPLASIA

Categorization of gestational trophoblastic neoplasia(National Cancer Instit

ute)A. Nonmetastatic disease: No evidence of disease outside uterus.B. Metastatic disease: Any disease outside uterus.

1. Good-prognosis metastatic disease- a. Short duration(< 4 months) b. Serum β-hCG < 40,000 mIU/ml c. No metastasis to brain or liver. d. No significant prior chemotherapy

2. Poor-prognosis metastatic disease- a. Long duration(> 4 months) b. Serum β-hCG > 40,000 mIU/ml c. Metastasis to brain or liver. d. Unsuccessful prior chemotherapy e. Gestational trophoblastic neoplasia following term pregnancy

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MALIGNANT GESTATIONAL TROPHOBLASTIC NEOPLASIA

• A Good-prognosis patients– Single-agent chemotherapy– Remission

• B Poor-prognosis patients– Combined chemotherapy

• Patients with poor-prognosis risk factors

• Revised FIGO ⅢC and Ⅳ• WHO scores > 7

– Regimens• MAC• CHAMOCA• EMA/CO

– Remission

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PLACENTAL-SITE TROPHOBLASTIC TUMOR

(PSTT)

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PLACENTAL-SITE TROPHOBLASTIC TUMOR(PSTT)

• PSTT occur with any type of pregnancy• derived from the intermediate trophoblasts• Invade myometrium and lymphatics• Treatment

– Hysterectomy– Partial uterine resection– Chemotherapy for metastatic cases

• EP-EMA• EMA/CO• Adverse outcomes

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Thank you