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GESTATIONAL
TROPHOBLASTIC DISEASE
MALIGNANT GESTATIONAL
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PREMALIGNANTNEOPLASIA
CONDITIONS
1.PARTIAL
VILLOUS
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INTERMEDIATE TROPHOBLASTMOLE
TROPHOBLAST
2.COMPLETE
PLACENTAL SITE TROPHOBLASTIC
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MOLE1.INVASIVE MOLE
TUMOUR
(PSTT)
2.CHORIOCARCINOMA
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EPITHELIOID TROPHOBLASTICTUMOUR
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#MALIGNANTGESTATIONALTROPHOBLASTICDISEASEorPERSITENTGESTATIONAL
TROPHOBLASTICDISEASE
Incidence is about 1 in 5000
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pregnancies in oriental countries50%-molar pregnancy
25% after abortion and ectopic
pregnancy and a few after normal
pregnancy
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Non metastatic (locally invasive}lesions-15%
Metastatic lesions -4% after molar
evacuation
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INVASIVEMOLES(80%)
POSTMOLAR
PREGNANCY
CHORIOCARCI
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GTNNOMAS(20%)
NON MOLAR
Almost always a
PREGNANCY
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CHORIOCARCINOMA
Persistent GTN is evidenced by the persistance of
trophoblastic activity following evacuation of
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molar pregnancy1
2
3
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After molar evacuation beta Hcg
become normal in about 7-9 weeks.
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GTN should be suspected in a women of
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reproductive age group presenting withmetastatic disease from an unknown primary
invasive mole
.
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CHORIADENOMA DESTRUENS
EXTENSIVE TISSUE INVASION BY
TROPHOBLAST AND WHOLE VILLI
PENETRATION IS DEEP INTO
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MYOMETRIUMSOMETIMES WITH THEINVOLVMENT OF THE PERITONEUM
ADJACENT PARAMETRIUM OR VAGINAL
VAULT.
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DIAGNOSIS
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CHORIOCARCINOMA
Carcinoma of the CHORIONIC
EPITHELIUM
Follows term pregnancy or miscarriage.
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Only third of cases follow a molar gestationChoriocarcinoma are commonly accompanied
by ovarian theca-lutein cysts.
PRIMARY SITE ANYWHERE IN UTERUS
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GROSS
MICROSCOPY
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HISTORYOFMOLARPREGNANCY/TERMPREGNANCY/ABORTION/ECTOPICPREGNANCY
A
hbenSyaomltrmhaluterinebleeding,Persitentill
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ptomspertain gtometastasielsewher1.Hemoptysi(lung-75%)
2
h.Feadtaurcheso,cfInvtraulsicroan.ciaolsmpaaceocupyinglesion-
3.Vaginalmetastasi(50%)
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4.MetastasialsocurtoVulva-iregularandat imesbriskhemorhage
Liver?epigastricpain,jaundice
Signs-patientlooksill,pallorofvaryingdegre
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BIMANUAL1.CHEST XRAY
EXAMINATION
2.PELVIC
SUBINVOLUTION
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SONOGRAPHY(toOF UTERUS
differentiate from
normal pregnancy
PURPLISH RED
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3.DIAGNOSTICNODULES IN THE
UTERINE CURETTAGE
LOWER THIRD OF
ANTERIOR
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4EXCISION BIOPSY OFVAGINAL WALL
VAGINAL NODULES
5.CT SCAN OR MRI OF
BRAINL,LIVER
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Histopathological diagnosis
on doing curettage for
irregular bleeding.
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Rapidly increasing levels ofserum beta hcg.
1.Chest x ray showing widespread metastatic lesions
2.Autopsy specimen with multiple hemorragic hepatic metastasis
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PLACENTAL SITE TROPHOBLASTIC
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Incidence-
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15-20% OF<1% of
PATIENTS
COMPOSED MAINLY OF
patients with
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DEVELOPGTN
METASTASIS
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*TREATMENT by hystrectomy ispreferred.
(locally invasive tumours are
ressistant to hystrectomy)
*For higher risk stage 1 and later
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stages,adjuvant multidrugchemotherapy is given.
*Arise from
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Primary treatment is hysterectomy becausethis tumor is relatively resistant to
chemotherapy.
Metastatic disease is common, and
combination chemotherapy is employed
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BETA
BIOPSY IS NOT
HCG
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USUALLYREQUIRED
SCORE
0
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12
4
AGE
<40
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> or =to-
-
40
ANTICEDENT
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MOLEAbortion
Term
-
PREGNANCY
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Interval after index<4
4-6
7-12
>12
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pregnancy(mo)Pretreatment serum beta <1000
1000-
10000- >or
hcg(mIU /mL)
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10,00010000 =to100000
0
Largest tumor
<3cm
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3-4cm>or=5 -
size(including uterus)
cm
Site of metastasis
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-Spleen,
GI
Liver, brain
kidney
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Number of metastasis-
1-4
5-8
8
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Previous failed-
-
1
> or=2
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chemotherapy drugsSTAGE 1
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DISEASE CONFINED TO THE UTERUSSTAGE 2
GTN EXTENDS OUTSIDE THE UTERUS BUT
LIMITED TO THE GENITAL STRUCTURES
(ADENEXA,VAGINA,BROAD LIGAMENT)
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STAGE 3GTN EXTENDS TO THE LUNGS WITH OR
WITHOUT GENITALTRACT INVOLVMENT
STAGE 4
ALL OTHER METASTATIC SITES
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