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Updated: Jul 22, 2025

Accurate and Simple Evaluation of Vascular Anastomoses in Monochorionic Placenta using Colored Dye
Published on: September 5, 2011
Large Chorioangioma in Triplets: An Uncommon Occurrence
Avin Kounsal1, Divya Saini2, Vivek Podder3
1Department of Diagnostic Radiology and Nuclear Medicine, Rush University Medical Center, Chicago, USA.
A rare placental tumor, angiomatous chorioangioma, complicated a triplet pregnancy, leading to preterm delivery and stillbirth. This case highlights the severe risks associated with large chorioangiomas in multiples.
Area of Science:
- Obstetrics and Gynecology
- Maternal-Fetal Medicine
- Pathology
Background:
- A 25-year-old primigravida at 26 weeks gestation presented for routine antenatal care.
- No prior history of pregnancy-induced hypertension (PIH) or edema was noted.
Observation:
- Physical examination revealed pallor and microcytic hypochromic anemia.
- Elevated beta-human chorionic gonadotropin (HCG) and alpha-fetoprotein (AFP) levels were detected.
- Ultrasound showed triplets with intertwining membranes, and the placenta had a large, hypoechoic mass with a central feeding vessel.
Findings:
- The anomaly scan showed no fetal abnormalities.
- Color Doppler confirmed a pulsatile feeding vessel within the placental mass.
- The patient delivered spontaneously at 28 weeks gestation; all three fetuses were stillborn.
Implications:
- Histopathological diagnosis confirmed angiomatous chorioangioma.
- Large chorioangiomas represent a grave complication in multiple gestations.
- This case underscores the importance of vigilant monitoring in high-risk pregnancies.
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