{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,15]],"date-time":"2026-01-15T22:08:22Z","timestamp":1768514902147,"version":"3.49.0"},"reference-count":9,"publisher":"BMJ","issue":"1","content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["BMJ Case Rep"],"accepted":{"date-parts":[[2018,12,20]]},"published-print":{"date-parts":[[2019,1]]},"abstract":"<jats:p>A 27-year-old multigravida woman was noted on routine growth scan at 27 weeks gestation to have a central placental hypoechoic area measuring 6.7\u00d76.0\u00d74.4\u2009cm. A subsequent magnetic resonance scan confirmed a solid mass in the placenta lying anteriorly; therefore, a preliminary diagnosis of giant placental chorioangioma was made. A repeat ultrasound scan at 30 weeks gestation indicated that the mass had increased, with the presence of polyhydramnios. The patient experienced reduced fetal movements at 31 weeks gestation. There was persistent fetal tachycardia at 33 weeks gestation, and consequently the neonate was delivered by emergency caesarean section. The placenta revealed a large chorioangioma. The neonate\u2019s birth weight was 2.85\u2009kg and non-immune hydrops fetalis was diagnosed. The neonate improved significantly in the neonatal intensive care unit and is currently well with no medical problems.<\/jats:p>","DOI":"10.1136\/bcr-2018-227828","type":"journal-article","created":{"date-parts":[[2019,1,30]],"date-time":"2019-01-30T23:09:15Z","timestamp":1548889755000},"page":"e227828","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":17,"title":["Placental chorioangioma associated with polyhydramnios and hydrops fetalis"],"prefix":"10.1136","volume":"12","author":[{"given":"Charlotte","family":"Willis","sequence":"first","affiliation":[{"name":"Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Siobhan","family":"Ferguson","sequence":"additional","affiliation":[{"name":"Women\u2019s Health, Royal Preston Hospital, Preston, UK"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fatimah","family":"Soydemir","sequence":"additional","affiliation":[{"name":"Women\u2019s Health, Royal Preston Hospital, Preston, UK"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[2019,1,29]]},"reference":[{"key":"2025082801455962000_12.1.e227828.1","doi-asserted-by":"crossref","first-page":"955","DOI":"10.2147\/IJWH.S72178","article-title":"Placental tumor (chorioangioma) as a cause of polyhydramnios: a case report","volume":"6","author":"Abdalla","year":"2014","journal-title":"Int J Womens Health"},{"key":"2025082801455962000_12.1.e227828.2","first-page":"30","article-title":"Placental chorioangioma: usual presentation and alternate treatment options","volume":"7","author":"Vaidyanathan","year":"2017","journal-title":"Journal of Case Reports"},{"key":"2025082801455962000_12.1.e227828.3","first-page":"170","article-title":"Chorioangiomas-new insights into a well-known problem. 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