Gestational Trophoblastic Disease Flashcards

1
Q

Gestational Trophoblastic Disease

A

From abnormal proliferation of placental = trophoblastic tissue (unique - fetal origin)

Malignant versions very chemosensitive (really curable; can preserve fertility)

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2
Q

Gestational Trophoblastic Disease tumor marker

A

Make hCG (tumor marker; for dx & following progression)

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3
Q

Potential consequences of Gestational Trophoblastic Disease

A

Remember hCG has common alpha subunit with LH/FSH/TSH

Can result in theca lutein cysts, hyperthyroidism, early PEC, hyperemesis

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4
Q

Benign GTD = “molar pregnancies” = “hyatidiform moles”

A

Highest in Asian women esp Japan (1/500!); extreme age, prior GTD; nullips are big risk factors too

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5
Q

Diagnosis of benign GTD

A

Dx: sx as described above, bleeding + early PEC, hyperthyroidism, etc.
PE: Uterus S>D; may see grape like clusters at os, palpate big theca lutein cysts
Pelvic U/S: “snowstorm” pattern
Definitive dx: pathologic examination

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6
Q

Complete / Classic Mole (90%) genetics

A

46,XX (all paternal)

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7
Q

Partial / Incomplete Mole (10%) genetics

A

69,XXY (extra paternal set)

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8
Q

Complete / Classic Mole pathology

A

No coexistent fetus / fetal RBC

Hydropic (swollen, ‘grape like’) villi

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9
Q

Partial / Incomplete Mole pathology

A

Coexistent fetus / RBC

No hydropic villi

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10
Q

Complete / Classic Mole presentation

A

No embryo
Presents with abnormal vaginal bleeding
Classic sx (hyperemiesis gravidarum, early PEC, hyperthyroidism, anemia, really big uterus S»D) common
Theca lutein cysts in 25%
hCG really high (>100,000), takes 14 wks to normalize

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11
Q

Partial / Incomplete Mole presentation

A
Yes embryo
Presents like missed Ab
Classic sx rare
Uterus S=D
Rare theca lutein cysts
hCG slightly elevated, takes 8 wks to normalize
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12
Q

Complete / Classic Mole malignant potential

A

15-25% nonmetastatic malignancy

4% metastatic malignancy

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13
Q

Partial / Incomplete Mole malignant potential

A

2-4% nonmetastatic

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14
Q

Treatment of benign GTD

A

IMMEDIATE D&C followed by IV oxytocin
Get baseline hCG first; Rh status to see if RhoGAM needed, CXR optional(?)
May need antiHTN meds if preeclamptic
May need beta blockers (propranolol) if thyroid storm
May do hysterectomy if done childbearing

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15
Q

Prognosis of benign GTD

A

95-100% cure rate
15-25% persistent disease
Follow up closely with serial hCGs until negative x 3 consecutive weeks, then monthly
Prevent pregnancy during the followup (otherwise can’t monitor hCG) with OCPs!!

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16
Q

Types of malignant GTD

A

Persistent / invasive moles (75%)
Choriocarcinoma (25%)
PSTT (really rare) = placental site trophoblastic tumors

17
Q

Persistent / invasive moles (75%)

A

Arise after evacuation of molar pregnancy: hydropic villi / tropoblasts invade myomet.
Rarely metastasize; can regress spontaneously

18
Q

Persistent / invasive moles diagnosis

A

Dx: plateauing / rising hCG after tx for molar pregnancy, can have uterine bleeding

19
Q

Persistent / invasive moles treatment

A

Tx: single agent chemo (MTX / actinomycin D) if low risk, multiagent if high risk

20
Q

Choriocarcinoma(25%)

A

Pure epithelial tumor; sheets of anaplastic cytotrophoblasts without villi.

21
Q

Presentation of choriocarcinoma

A

Malignant, necrotizing, arises weeks/years after pregnancy
Often metastatic, can spread hematogenously (lungs / vagina / pelvis / brain / liver / GI)
Present with late postpartum bleeding or irregular bleeding years later
Mets to lungs → cough, resp distress, hemoptysis

22
Q

Diagnosis of choriocarcinoma

A

Only a positive beta-HCG in a reproductive-aged woman who has a history of a recent pregnancy (term, miscarriage, termination, mole) is necessary to establish the diagnosis

(Tissue diagnosis is the standard in establishing a diagnosis of most all malignancies, with the exception of choriocarcinoma.)

23
Q

Work up for choriocarcinoma

A

Get hCG, CBC/coags, pelvic U/S (doppler → really vascular), CXR/chest CT for lungs, abd/pelvic CT or MRI to look for mets as well

24
Q

Treatment for choriocarcinoma

A

Tx: single agent chemo / multiagent chemo depending on prognosis

25
Q

PSTT (really rare) = placental site trophoblastic tumors

A

Arise from placental implantation site; no villi, intermediate trophoblasts proliferating
Persistent irregular vaginal bleeding + big uterus
Chronic low levels of hCG (no syncitiotrophoblasts proliferating)

26
Q

Treatment of PSTT

A

Treat with hysterectomy → multiagent chemo 1 week later to prevent recurrence

27
Q

Malignant GTD

A

Metastatic if beyond uterus; bad prognosis if metastatic and bHCG > 40,000, duration > 4mo, mets to brain or liver, chemo failure, GTD after a term pregnancy
Staging not clinically useful
Really chemosensitive - NO ROLE FOR SURGERY unless high risk or PSTT
Follow bHCG