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Essentials of Diagnosis
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General Considerations
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Gestational trophoblastic disease is a spectrum of disorders, including
Hydatidiform mole (partial and complete)
Invasive mole (local extension into the uterus or vagina)
Choriocarcinoma (malignancy often complicated by distant metastases)
Placental site trophoblastic tumor
Complete moles show no evidence of a fetus on ultrasonography; the majority are 46, XX with all chromosomes of paternal origin
Partial moles generally show evidence of an embryo or gestational sac; are triploid, slower-growing, and less symptomatic; and often present clinically as a missed abortion
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Highest rates of gestational trophoblastic neoplasia occur in Asians
Risk factors include prior spontaneous abortion, a history of mole, and age below 21 or above 35
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Differential Diagnosis
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High serum β-hCG subunit values
Can range from high normal to the millions
Levels are higher with complete moles than with partial moles
Can cause the release of thyroid hormone, and rarely, symptoms of hyperthyroidism will be present
Serum β-hCG values are more helpful in managing response to treatment than they are for diagnosis
Hematocrit, creatinine, blood type, liver chemistries, and thyroid function tests
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Preoperative diagnosis is made with ultrasonography
Placental vesicles can be easily seen on transvaginal ultrasound
Preoperative chest radiograph is required to evaluate for pulmonary metastases of trophoblast
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