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Gestational trophoblastic disease I: epidemiology, pathology, clinical presentation and diagnosis of gestational trophoblastic disease, and management of hydatidiform mole

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Gestational trophoblastic disease includes hydatidiform mole (complete and partial) and gestational trophoblastic neoplasia (invasive mole, choriocarcinoma, placental site trophoblastic tumor, and epithelioid trophoblastic tumor). The epidemiology, pathology, clinical presentation, and diagnosis of each of these trophoblastic disease variants are discussed. Particular emphasis is given to management of hydatidiform mole, including evacuation, twin mole/normal fetus pregnancy, prophylactic chemotherapy, and follow-up.

Section snippets

Epidemiology

The incidence and etiologic factors contributing to the development of GTD have been difficult to characterize. The problems in accumulating reliable epidemiologic data can be attributed to a number of factors, such as inconsistencies in case definitions, inability to adequately characterize the population at risk, no centralized databases, lack of well-chosen control groups against which to compare possible risk factors, and rarity of the diseases.4

Epidemiologic studies have reported wide

Pathology

Molar pregnancies and gestational trophoblastic neoplasms all take their origin from the placental trophoblast. Normal trophoblast is composed of cytotrophoblast, syncytiotrophoblast, and intermediate trophoblast. Syncytiotrophoblast invades the endometrial stroma with implantation of the blastocyst and is the cell type that produces human chorionic gonadotropin (hCG). Cytotrophoblast functions to supply the syncytium with cells in addition to forming outpouchings that become the chorionic

Complete hydatidiform mole

Complete hydatidiform mole most commonly presents with vaginal bleeding, usually occurring at 6-16 weeks of gestation in 80-90% of cases. The other classic clinical signs and symptoms, such as uterine enlargement greater than expected for gestational dates (28%), hyperemesis (8%), and pregnancy-induced hypertension in the first or second trimester (1%), occur less frequently in recent years because of earlier diagnosis as a result of widespread use of ultrasonography and accurate tests for hCG.

Ultrasonography

Ultrasonography plays a critical role in the diagnosis of both complete and partial mole, and it has virtually replaced all other means of preoperative diagnosis.38, 43, 44, 45 Because the chorionic villi of complete moles exhibit diffuse hydropic swelling, a characteristic vesicular ultrasonographic pattern can be observed, consisting of multiples echoes (holes) within the placental mass and usually no fetus (Figure 6). Ultrasonography may also facilitate the early diagnosis of a partial mole

Treatment

Once the diagnosis of molar pregnancy is suspected by history, physical examination, hCG levels, and ultrasound findings, the patient should be evaluated for the presence of medical complications (anemia, preeclampsia, hyperthyroidism) by way of vital signs and laboratory tests, such as complete blood cell counts, basic chemistry, hepatic and thyroid panels, urinalysis, and chest x-ray. The preoperative evaluation should also include blood type and crossmatch, serum hCG level, and

Follow-up after molar evacuation

Follow-up after evacuation of a hydatidiform mole is essential to detect trophoblastic sequelae (invasive mole or choriocarcinoma), which develop in approximately 15-20% with complete mole and 1-5% with partial mole.59, 70, 71, 72, 73, 74 Clinical findings of prompt uterine involution, ovarian cyst regression, and cessation of bleeding are all reassuring signs, however, definitive follow-up requires serial serum quantitative hCG measurements every 1-2 weeks until 3 consecutive tests show normal

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