MedElevator
Войти в исследования Taiwanese journal of obstetrics & gynecology · 2025
Complete mole with co-existing fetus: a rare case report of full-term delivery with favorable maternal and fetal outcomes.
Клинический случайСтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Liuqin Hu, Na Wang, Huimin Zhang, Shaoying Li, Yinong Xie, Zhiguang Yuan, Min Chen, Yingtao Li, Zhihua Li, Dunjin Chen
Аннотация
OBJECTIVE: To explore the obstetric and oncological outcomes of CHMCF and to give a beneficial reference for the individualized management of the disease and the timing of pregnancy termination.
CASE REPORT: A 25-year-old primipara was diagnosed with CHMCF at 17 weeks of gestation by prenatal ultrasound. Magnetic resonance imaging, genetics and consanguinity identification testing were performed. There were no serious pregnancy complications. At 38 weeks of gestation, a small-for-gestational-age fetus was delivered by cesarean section, and there was no obvious abnormality in postpartum follow-up.
CONCLUSION: CHMCF belongs to paternal diploid twin pregnancy. Ultrasound and magnetic resonance imaging are important methods for early diagnosis. When the fetal karyotype is normal and there is no obvious pregnancy complication, it is feasible to continue pregnancy, and the incidence of GTN is not significantly increased compared with the termination of pregnancy.
CASE REPORT: A 25-year-old primipara was diagnosed with CHMCF at 17 weeks of gestation by prenatal ultrasound. Magnetic resonance imaging, genetics and consanguinity identification testing were performed. There were no serious pregnancy complications. At 38 weeks of gestation, a small-for-gestational-age fetus was delivered by cesarean section, and there was no obvious abnormality in postpartum follow-up.
CONCLUSION: CHMCF belongs to paternal diploid twin pregnancy. Ultrasound and magnetic resonance imaging are important methods for early diagnosis. When the fetal karyotype is normal and there is no obvious pregnancy complication, it is feasible to continue pregnancy, and the incidence of GTN is not significantly increased compared with the termination of pregnancy.