Intraplacental choriocarcinoma is rare, and occasionally results in massive feto-maternal hemorrhage. We describe a case of an intraplacental choriocarcinoma diagnosed postpartum after a preterm cesarean delivery of a severely anemic newborn. The microscopic examination showed that clusters of malignant trophoblasts arose from residual normal chorionic villi and infi ltrated into the intervillous spaces, confirmed as intraplacental choriocarcinoma. Fetomaternal hemorrhage is a rare complication of choriocarcinoma but its presence should always warrant detailed examination of placenta, mother, and infant.Keywords: Fetomaternal hemorrhage; Fetal distress; Intraplacental choriocarcinoma CASE REPORT Received: 2011. 8.18. Revised: 2011. 9.21. Accepted: 2011 Gestational trophoblastic disease encompasses a spectrum of interrelated tumors, including the hydatidiform moles, either partial or complete, to the more malignant forms, the invasive mole, the placental site and epithelioid trophoblastic tumors and choriocarcinoma [1]. Intraplacental choriocarcinoma, defi ned as choriocarcinoma in the placenta, is a rare variant of gestational choriocarcinoma accounting for no more than approximately 0.04% of gestational trophoblastic disease [2]. Older than 35 years or very young age of mother can be risk factors of gestational trophoblastic disease [3]. As fetomaternal hemorrhage can cause fetal distress and death, the possibility of intraplacental choriocarcinoma should be considered in these cases [4]. In this report, we present a case of an incidental intraplacental choriocarcinoma that was discovered when the placenta was examined in order to identify the cause of a newborn's anemia.
Case ReportA 27-year-old woman, gravida 1, was referred to our institution for evaluation of fetal cardiomegaly and ascites at 31+4 weeks' gestation. Her past history was uneventful, and the results of antenatal laboratory tests and examinations were normal. The mother presented with decreased fetal movement from around 31 weeks of gestation. A transabdominal ultrasound scan with 3.5-5 MHz trasducers (Accuvix XQ, Medison, Seoul, Korea) revealed a severely dilatated heart, skin edema, pleural effusion and ascites, suggesting fetal hydrops. Cardiotocography was severely pathologic, showing a repeatitive late decerelation and decreased variability (Fig. 1). Emergency cesarean delivery was performed because of fetal hydrops and fetal distress. At delivery, the newborn baby weighed 2,020 g and had Apgar scores of 3 at 1 minute and 5 at 5 minutes. The baby was immediately intubated due to weak respiratory movement and was mechanically ventilated in the neonatal intensive care unit. He was markedly anemic and edematous. Initial chest X-ray showed a total white out pattern on the both lung fi elds. After admission, the baby's condition deteriorated