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Gestational Trophoblastic Disease. DI WEN M.D., Ph.D., Professor & Chairman Department Of Obstetrics & Gynecology Renji Hospital Affiliated to SJTU School of Medicine.

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gestational trophoblastic disease

Gestational Trophoblastic Disease

DI WEN M.D., Ph.D.,

Professor & Chairman

Department Of Obstetrics & Gynecology

Renji Hospital Affiliated to SJTU School of Medicine

GTD

introduction
introduction
  • Defination:
    • gestational trophoblastic disease (GTD) is a group of disease originated from placental villose trophoblastic cells, including hydatidiform mole, invasive mole, choriocarcinoma and a kind of less common trophoblastic cell tumor in placenta.
introduction3
introduction
  • Relations among the diseases:
    • Benign moleis considered to be abnormal formation of placenta accompanied by the special abnormal hereditary ;
    • Invasive moleresults from benign mole;
    • Choriocarcinoma and the trophoblastic cell tumor in placentamay result from benign mole, term pregnancy, abortion and ectopic pregnancy.
introduction5
Introduction
  • Defination:hydatidiform mole means that after pregnancy the placental trophoblastic cells proliferate abnormally, there is stromal edema, and forms vesicula which is like grape on its apparence.
  • Classification :hydatidiform mole is divided into complete and incomplete type
etiology
Etiology
  • the etiology is not clear
  • Etiology of complete hydatidiform mole

Epidemiology: the morbidity of hydatidiform mole is different in different area.

High risk factors:

1.nourishing status,social economy.

2.age:over 35 and 40 years old;below 20 years old.

3.hydatidiform mole history:if a patient has the history of 1 or 2 times hydatidiform mole,then the morbidity of the hydatidiform mole when pregnant again is 1% and 15~20% respectively.

Genetic factors:

1.enucleate egg fertilization: chromosome karyotype of complete mole is diploid ,90% is 46XX,10% is 46XY.

etiology8
Etiology
  • Etiology of incomplete hydatidiform mole
    • the morbidity of incomplete mole is much lower than that of the complete type, and it is not associated with age.
    • Genetic factors: chromosome karyotype of 90% incomplete mole is triploid. The most common chromosome karyotype is 69XXY,and then is 69XXX or 69XYY.
pathology
Pathology

Complete mole incomplete mole

Embryotic or fetal tissue -+

Villus stromal edema diffuseed localized

Trophoblastic hyperplasia diffuseed localized

Villus outline regular irregular

Villus stromal blood vessel -+

Karyotype diploid triploid or tetraploid

slide11

Partial mole

Complete mole

slide12

Partial mole

Complete mole

clinical manifestation
Clinical manifestation
  • complete mole:
    • vaginal bleeding after amenorrhea
    • uterus is abnormally enlarged and become soft
    • hyperthyroidism
    • theca lutein ovarian cyst
    • gestational vomitting and PIH
    • Hyperthyroidism
clinical manifestation15
Clinical manifestation
  • partial mole:
    • may have the major symptoms of complete mole but it is slightly manifested. no luteinizing cyst. The histologic examination of curettage sample may confirm the diagnosis.
prognosis
Prognosis
  • complete mole has the latent risk of local invasion or telemetastasis
  • The high-risk factors includes
    • β-HCG>100000IU/L
    • uterine size is obviously larger than that with the same gestational time.
    • the luteinizing cyst is >6cm
    • If >40 years old,the risk of invasion and metastasis may be 37%, If >50 years old,the risk of invasion and metastasis may be 56%.
    • repeated mole:the morbidity of invasion and metastasis increase 3~4 times
diagnosis
Diagnosis
  • HCG measurement
  • ultrasound examination
  • detecting the fetal heart beat by ultrasound Doppler
differential diagnosis
Differential diagnosis
  • abortion
  • twin pregnancy
  • polyhydramnios
management
Management
  • emptying uterine cavity
    • once the diagnosis is confirmed the uterine cavity should be emptied as soon as possible
  • Hysterectomy
    • over 40 years old with high-risk factors
    • uterine size is over 14 gestational weeks
  • management of luteinizing cyst
management21
Management
  • preventive chemotherapy
    • over 40 years old
    • the β-HCG is over 100kIU/L before emptying mole
    • the HCG regresion curve is not progressively declined
    • uterus is obviously larger than the size of the amenorrhea
    • luteinizing cyst is >6cm
    • there is still over hyperplasia of trophoblastic cells in the second curettage
    • no follow up conditions
follow up
Follow up
  • HCG qw till normal
  • QW X 3m
  • Q2W X 3m
  • QM X 6m
  • Q6M X 2y
introduction24
introduction
  • Definition: Invasive molemeans the hydatidiform mole invade the uterine myometrium or metastasize to extrauterine tissue.
  • Biologic behavior: invasive mole villus may invade myometrium or blood vessels or both, at beginning it spread locally,invade myometrium, sometimes penetrate the uterine wall and spread to the broad ligament or abdominal cavity.
pathology25
Pathology
  • Macro examination: different size of viscula in myometrium,there may be or may not be primary focus in uterine cavity.when the invasion is near serosal layer……
  • Microexamination:villose structure and trophoblastic cells proliferation and differentiation deficiency.villose and trophoblastic cells can be found in most patients,and causevascular wall necrosis and bleeding
clinical manifestation26
Clinical manifestation
  • irregular vaginal bleeding
  • uterine subinvolution
  • theca lutein cyst does not disappear after emptying uterus
  • abdominal pain
  • metastatic focus manifestation
diagnosis27
Diagnosis
  • history and clinical manifestation
  • successive measurement of HCG
  • ultrasound examination
  • X-ray and CT
  • histologic diagnosis
introduction29
Introduction
  • Choriocarcinoma is a highly malignant tumor,it can metastasize to the whole body through blood circulation , damage tissues and organs,cause bleeding and necrosis.
  • The most common metastatic site is lung ,then vagina,brain and liver
  • 50%gestational choriocarcinoma result from hydatidiform mole (generally occurs over 1 year after emptying the mole),the rate of occurrence after abortion or term delivery is 25% and 25% respectively, seldom occurs after ectopic pregnancy
pathology30
Pathology
  • macroexamination: most choriocarcinoma occurs in uterus, the tumor diameter 2-10cm, its color, section, cancer embolus is often found in parauterine veins,ovarian luteinizing cystmay be formed
  • histologic examination: under microscope the hyperplastic cytotrophoblastic cells and syntrophoblastic cells invade the myometrium and blood vessels accompanied by the bleeding and necrosis, so the cancer cells can notbe found in the center
clinical manifestation32
Clinical manifestation
  • Vaginal bleeding
  • Pain
  • Uterine enlargement
  • Mass
diagnosis33
Diagnosis
  • Clinical Features
  • Ultrasonography
  • Human Chorionic Gonadotrophin
  • CT
  • X-ray
  • Pathology
differential diagnosis34
Differential diagnosis
  • Hydatidiform mole
  • Invasive mole
  • Placental site trophoblastic tumors
  • Rudimental placenta
metastases
Metastases
  • Lung
  • Vagina
  • Brain
  • Liver
anatomic staging
anatomic staging
  • Stage I disease confined to uterus
  • Stage II gestational trophoblastic tumor extending outside uterus but limited to genital structures (adnexa, vagina, broad ligament)
  • Stage III gestational trophoblastic disease extending to lungs with or without known genital tract involvement
  • Stage IV all other metastatic sites
management38
Management
  • Chemotherapy
  • Surgery
follow up39
Follow up
  • QM X 1 y
  • Q3M X 2 y
  • QY X 2y
  • Q2Y
slide40

Thanks for Your Attention

DI WEN M.D., Ph.D.

Professor & Chairman

Department of Obstetrics & Gynecology

Renji Hospital Affiliated to SJTU School of Medicine

GTD