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Multiple giant placental chorioangioma: A case report
Atefe Hashemi1, Shaghayegh Moradi Alamdarloo1, Homeira Vafaei1
1Maternal-Fetal Medicine Research Center, Department of Obstetrics and Gynecology, School of Medicine Shiraz University of Medical Sciences Shiraz Iran.
Giant chorioangiomas are rare placental tumors that can cause serious fetal and maternal complications. Early detection and individualized management, including ultrasound monitoring, are vital for improving outcomes.
Area of Science:
- Obstetrics and Gynecology
- Fetal Medicine
- Pathology
Background:
- Chorioangiomas are benign placental tumors affecting ~1% of pregnancies.
- Giant chorioangiomas (>4cm) are rare but carry significant maternal and fetal risks.
Observation:
- A case of multiple giant chorioangiomas in a 23-year-old woman at 28 weeks gestation.
- Ultrasound revealed fetal anomalies including cleft lip/palate and cardiac/lung abnormalities.
- The neonate presented with hydrops fetalis and unfortunately passed away shortly after birth.
Findings:
- Giant chorioangiomas can lead to arteriovenous shunting, compromising fetal perfusion and causing cardiac failure.
- Diagnostic tools like Doppler ultrasound and MRI aid in distinguishing these tumors.
- Management requires a multidisciplinary approach tailored to gestational age and maternal-fetal status.
Implications:
- Timely, individualized treatment plans are crucial for managing fetal compromise and reducing mortality.
- Consistent ultrasound monitoring, Doppler flowmetry, and amniotic fluid assessment are key for conservative management.
- Further research is needed to elucidate chorioangioma mechanisms and establish comprehensive guidelines.
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