Suraj 23 H Mole
Suraj 23 H Mole
Hydatiform mole
Chromosomal composition:
Complete H.mole- 46XXY (single sperm fertilizes egg that has lost its chromosomes)
Partial H. mole – 69XXY (fertilization of a normal egg by two sperms)
Location: Uterus; rarely ovaries or fallopian tubes, chorionic villi are converted to mass of clear
vesicles that resemble bunch of grapes.
Risk factors:
Moles are more common in ages over 40, and prior moles makes you more likely to get
another mole.
Complete Mole (classic mole) (70%): This one involves the entire placenta. There will be no
fetus. The worthless trivia is that the karyotype is diploid. The pathogenesis is fertilization of an
egg that has lost its chromosomes (46, XX).
First Trimester US: Classically shows the uterus to be filled with an echogenic, solid, highly
vascular mass, often described as “snowstorm” in appearance.
May be difficult to diagnose in the first trimester
o may appear similar to a normal pregnancy or as an empty gestational sac
o <50% are diagnosed in the first trimester
Second Trimester US: Vesicles that make up the mole enlarge into individual cysts (2-30 mm)
and produce your “bunch of grapes” appearance.
Bilateral theca lutein cysts may also be seen on ultrasound.
CT: low resolution for assessment, hypoattenuating regions surrounding by enhancing
myometrium.
MRI: MRI may demonstrate a heterogeneous mass with cystic spaces distending the uterine
cavity. Fetal parts are notably absent.
Partial Mole (30%): This one involves only a portion of the placenta. You do have a fetus, but
it’s all jacked up (triploid in karyotype). The pathogenesis is fertilization of an ovum by two
sperm (69, XXY(70%)/XXX(27%)/XYY(3%)). It’s lethal to the fetus. Less likely to progress to
choriocarcinoma.
US: The placenta will be enlarged, and have areas of multiple, diffuse anechoic lesions , cystic
spaces. Well-formed but growth-retarded fetus, either dead or alive with hydropic degeneration of fetal parts
being frequently present. Theca Lutein cysts may be +. Most commonly bilateral and seen in the
second trimester.
Some partial moles can have sonographic appearances indistinguishable from those of the
common complete moles or missed abortions, although an echogenic rim around the sac, as
found in missed abortion or blighted ovum, is notably absent.
CT: CT evaluation is not usually performed given its low resolution for the uterine assessment.
CT may show an enlarged uterus with areas of low attenuation, or hypoattenuating foci
surrounded by highly enhanced areas in the myometrium.
MRI: MRI can be used to determine if there is an extension of molar tissue outside the uterus.
Treatment and prognosis: When a partial mole is suspected and there is a live fetus, counseling
and genetic tests looking for triploidy should be offered (chorionic villus
sampling or amniocentesis).
Suction and curettage are used for evacuation and close follow-up of serum hCG levels for 6
months.
Buzzwords: Enlarged uterus, markedly elevated B-hCG, hyperemesis , theca lutein cysts
Invasive Mole
This refers to invasion of molar tissue into the myometrium. You typically see it after the
treatment of a hydatidiform mole (about 10% of cases). US may show echogenic tissue in
the myometrium. However, MRI is way better at demonstrating muscle invasion. MRI is going
to demonstrate focal myometrial masses, dilated vessels, and areas of hemorrhage and
necrosis.
Choriocarcinoma
This is a very aggressive malignancy that forms only trophoblasts (no villous structure).
Spread locally (into the myometrium and parametrium) then to spread hematogenous to any site
in the body. Very vascular and bleeds. The classic clinical scenario is serum β-hCG levels that
rise in the 8 to 10 weeks following evacuation of molar pregnancy. On ultrasound,
choriocarcinoma (at any site) results in a highly echogenic solid mass. Treatment =
methotrexate.