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- W2003173234 abstract "The purpose of this study was to provide a diagnostic and a prognostic variable that could easily be measured in the laboratory, and that would predict the need for future therapy of persistent gestational trophoblastic disease. There would no longer be a need to treat all cases of hydatidiform mole prophylactically, to improve the outcome in only about 20% predicted to develop malignant gestational trophoblastic tumors. Circulating β-human chorionic gonadotropin (β-hCG), progesterone, 17β-estradiol and inhibin levels were measured using standard radioimmunoassays in 60 patients with complete hydatidiform mole and in 20 normal pregnant women of a corresponding duration of pregnancy and having a maternal indication for therapeutic abortion. There were no significant statistical differences between the two groups as regards gravidity, parity and gestational age. There was a significant statistical difference between patients with a molar pregnancy who developed gestational trophoblastic tumors (GTT) and those who did not develop GTT as regards pre-evacuation and follow-up mean serum β-hCG, mean serum progesterone and mean serum 17β- estradiol levels. These findings together with the persistently elevated mean serum progesterone and mean serum 17β-estradiol levels at 6 weeks after evacuation in all cases who developed GTT suggested that progesterone as well as 17β-estradiol serum levels might be of prognostic value in cases of molar pregnancy. However, larger numbers of cases are required to correlate findings to β-hCG serum level. Although mean serum inhibin level was significantly higher in women with hydatidiform mole than in normal pregnant women, it lacks any prognostic value for detection of subsequent gestational trophoblastic tumors." @default.
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- W2003173234 date "2004-01-01" @default.
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- W2003173234 title "The prognostic value of serum inhibin, 17β-estradiol and progesterone in cases of hydatidiform mole" @default.
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- W2003173234 doi "https://doi.org/10.1080/09513590310001652991" @default.
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