Gestational Trophoblastic Disease Flashcards
Gestational Trophoblastic Disease
From abnormal proliferation of placental = trophoblastic tissue (unique - fetal origin)
Malignant versions very chemosensitive (really curable; can preserve fertility)
Gestational Trophoblastic Disease tumor marker
Make hCG (tumor marker; for dx & following progression)
Potential consequences of Gestational Trophoblastic Disease
Remember hCG has common alpha subunit with LH/FSH/TSH
Can result in theca lutein cysts, hyperthyroidism, early PEC, hyperemesis
Benign GTD = “molar pregnancies” = “hyatidiform moles”
Highest in Asian women esp Japan (1/500!); extreme age, prior GTD; nullips are big risk factors too
Diagnosis of benign GTD
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
Complete / Classic Mole (90%) genetics
46,XX (all paternal)
Partial / Incomplete Mole (10%) genetics
69,XXY (extra paternal set)
Complete / Classic Mole pathology
No coexistent fetus / fetal RBC
Hydropic (swollen, ‘grape like’) villi
Partial / Incomplete Mole pathology
Coexistent fetus / RBC
No hydropic villi
Complete / Classic Mole presentation
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
Partial / Incomplete Mole presentation
Yes embryo Presents like missed Ab Classic sx rare Uterus S=D Rare theca lutein cysts hCG slightly elevated, takes 8 wks to normalize
Complete / Classic Mole malignant potential
15-25% nonmetastatic malignancy
4% metastatic malignancy
Partial / Incomplete Mole malignant potential
2-4% nonmetastatic
Treatment of benign GTD
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
Prognosis of benign GTD
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!!
Types of malignant GTD
Persistent / invasive moles (75%)
Choriocarcinoma (25%)
PSTT (really rare) = placental site trophoblastic tumors
Persistent / invasive moles (75%)
Arise after evacuation of molar pregnancy: hydropic villi / tropoblasts invade myomet.
Rarely metastasize; can regress spontaneously
Persistent / invasive moles diagnosis
Dx: plateauing / rising hCG after tx for molar pregnancy, can have uterine bleeding
Persistent / invasive moles treatment
Tx: single agent chemo (MTX / actinomycin D) if low risk, multiagent if high risk
Choriocarcinoma(25%)
Pure epithelial tumor; sheets of anaplastic cytotrophoblasts without villi.
Presentation of choriocarcinoma
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
Diagnosis of choriocarcinoma
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.)
Work up for choriocarcinoma
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
Treatment for choriocarcinoma
Tx: single agent chemo / multiagent chemo depending on prognosis
PSTT (really rare) = placental site trophoblastic tumors
Arise from placental implantation site; no villi, intermediate trophoblasts proliferating
Persistent irregular vaginal bleeding + big uterus
Chronic low levels of hCG (no syncitiotrophoblasts proliferating)
Treatment of PSTT
Treat with hysterectomy → multiagent chemo 1 week later to prevent recurrence
Malignant GTD
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