Multiple Giant Placental Chorioangioma: A Case Report

• DOI: 10.22541/au.171654996.64086434/v1
• Publication Date: 2024-05-24T11:26:06Z
• Authors: Atefe Hashemi; Shaghayegh Moradi...; Homeira Vafaei; Hamide Barzegar; Firoozeh Jafari; Sara Haseli; Elahe Abbaspour
• Keywords: placental chorioangioma; Medicine (General); R; Case Report; giant chorioangioma; Doppler ultrasound; 03 medical and health sciences; R5-920; 0302 clinical medicine; placental tumor; case report; Medicine

Introduction Chorioangioma is a benign vascular tumor of the placenta that occurs in approximately 1% pregnancies1. The majority cases are small and asymptomatic, with symptoms appearing only 0.01%–0.03% instances2. Giant chorioangiomas, defined as tumors larger than 4 cm, remarkably rare, prevalence ranging from 1:9,000 to 1:50,000 3. While many chorioangiomas detected during postnatal examination placental histology, large associated significant maternal fetal complications. These include preterm labor, intrauterine growth restriction (IUGR), pre-eclampsia, polyhydramnios well hydrops fetalis, disseminated intravascular coagulation (DIC), mortality 4–6.Despite advancements therapeutic approaches, perinatal rates remain high, estimated be more 30%7. Therefore, it essential highlight importance timely identification, comprehensive prenatal monitoring, appropriate interventions prevent morbidity mortality8. In this report, we present case involving multiple giant 23-year-old woman, which were complications ultimately resulted neonate's death due fetalis. This emphasizes complexity condition underscores necessity for multidisciplinary approach evaluating counseling patients intricate anomalies. study has been reported line CARE criteria9.