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History
• 21 years G3 P1 M1
• Normal vaginal delivery 10 months ago
• Depo-Provera after delivery, now abnormal menses
• Feels and looks healthy
Examination
• Normal observations
• Normal general and systemic examination
• Gynecological examination: Bulky uterus
Management
• Referred for pelvic ultrasound as first line investigation

Differential
diagnosis
1. Invasive mole
2. Choriocarcinoma
Other
investigations
• Beta-HCG
• CXR
• Brain CT
• Liver functions and liver scan
The
patient was managed by the clinicians as a young patient with choriocarcinoma
CHORIOCARCINOMA
Gestational
trophoblastic neoplasia represents a spectrum of diseases of which
choriocarcinoma known to be one of the most malignant neoplasms affecting women.
This epithelial tumor is composed of highly anaplastic strands of interlacing
syncytiotrophoblastic and cytotrophoplasic elements.
Classification
of gestational trophoblastic neoplasms:
1. Histopathologic:
• Molar pregnancy (hydatidiform mole)
• Infiltrating molar pregnancy (chorioadenoma destruens)
• Choriocarcinoma
2. Clinical:
• Benign
• Malignant
3. Morphological:
• Complete mole
• Incomplete mole
Incidence
• Common in Asia 1:85 pregnancies
• Taiwan 1:120
• South-Africa 1:2000
• Increased risk in the age groups younger than 20 years and older than 40 years
and a history of previous miscarriage or molar pregnancy
Ultrasound
diagnosis
Gray
scale imaging:
Making
the diagnosis hydatidiform mole is important because after the mole has been
evacuated from the uterus these women must have careful follow-up to exclude
subsequent development of choriocarcinoma. The classic ultrasound
appearance of a hydatiform mole will result in multiple small sonolucent areas
which correspond to the "grape-like" vesicles that one sees on gross
pathologic examination. When the products of conception undergo further
hydropic change and proliferation with neo-vascularization a chorio-carcinoma
develops. On ultrasound the tissue becomes more hyperechoic with less
sonolucent areas. Refer to images.
Colour
doppler:
Typically
displays a colour-coded "hot" area representing pre-existing and
newly formed vessels. All of these vessels show high-velocity, low-impedance
blood flow signals. Colour Doppler flow imaging and pulsed Doppler
can be used to evaluate chemotherapeutic results
Interesting
fact!
Choriocarcinoma
tissue does not contain any HLA anti-bodies( like sperms) which may explain way
it is so highly malignant - the body does not recognize it as foreign.
References:
-
Kurjack
A, Kupesic S. An Atlas of transvaginal Colour doppler(2nd edition)
.The Parthenon Publishing Group ,2000;75 -8
-
Jauniaux
E, Gavriil P, Nicolaides K. Ultrasonographic assessment of early
pregnancy complications. In Jurkovic d,Jauniaux,eds. Ultrasound and
Early Pregnancy. Carnforth, UK: Parthenon Publishing,1996:53-64
-
Berkowittz
RS, Golstein DP, Bernstein MR. Evolving concepts of molar pregnancy. J
Reprod Med 1991;36:40 - 4
-
Aoki
S,Hata H, Hata K, et al .Doppler colour flow mapping on an invasive mole. Gynecol
Obstet Invest 1989;27:52 -4
-
HsiehFJ
,Wu CC,Lee CN,et al. Vascular patterns of gestationla trophoblastic tumors
by colour Doppler ultrasound. Cancer 1994;74:2361-5
-
Lindholm
H, Radestad A ,Flam F. Hysteroscopy provides proof of trophoblastic tumors
in the three in cases with negative colour Doppler images. Ultrasound
Obstet Gynecol 1997;9:59 -61.
-
Goldstein
RS, Timor-trich IE. Ultrasound in Gynecology(1st edition). Churchhill
Livingstone Inc,1995:163 -4
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