Radiofrequency thermal ablation of giant placental chorioangioma complicated with fetal hydrops: a case report and successful outcome

IF 0.1 Q4 OBSTETRICS & GYNECOLOGY
Jack Hamer, Leo Gurney, Shireen Meher, Robert Negrine, V. Hodgetts Morton, Tamas Marton, R. K. Morris
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Abstract

Chorioangiomas are the most frequently occurring type of benign tumour of the placenta. However, large chorioangiomas greater than 4 cm are rare and can be more frequently associated with serious complications such as: polyhydramnios, hydrops fetalis, fetal anaemia, intrauterine growth restriction, preterm birth, and an increased risk of perinatal mortality. Importantly timely prenatal diagnosis with close surveillance alongside potential intrauterine intervention can prove impactful on pregnancy outcome and fetal survival. We present a case of a 36-year-old female referred to our tertiary fetal medicine unit at 28 weeks’ gestation with a large chorioangioma measuring 9.4×8.8×5.5 cm and ultrasonographic evidence of severe fetal anaemia and fetal hydrops. The patient underwent an intrauterine transfusion and in utero surgical therapy with radiofrequency ablation (RFA). Immediately following the procedure, the fetus sustained a period of bradycardia, followed by asystole. Delivery was expedited via emergency caesarean section. Careful planning and rapid delivery after fetal intervention within the most appropriate surgical setting mitigated risks for the baby and resulted in a positive outcome. The baby was discharged from the neonatal unit on day 84 of life. Large placental chorioangiomas are a rare occurrence, however, when associated with fetal complications present a high incidence of adverse perinatal outcomes. In utero interventions require careful planning and surgical expertise to ensure improved fetal and neonatal outcomes. To the best of our knowledge this case is the first recorded instance of a successful postnatal outcome following RFA for a large placental chorioangioma, whereby the fetus was complicated by fetal hydrops.
巨大胎盘绒毛血管瘤并发胎儿水肿的射频热消融术:病例报告和成功结果
绒毛膜血管瘤是最常见的胎盘良性肿瘤。然而,大于 4 厘米的巨大绒毛膜血管瘤并不多见,而且更常见于严重的并发症,如:多胎畸形、胎儿水肿、胎儿贫血、胎儿宫内生长受限、早产以及围产期死亡风险增加。重要的是,及时的产前诊断、密切的产前监护以及潜在的宫内干预可对妊娠结局和胎儿存活产生影响。 我们介绍了一例 36 岁女性在妊娠 28 周时因巨大脉络膜血管瘤(9.4×8.8×5.5 厘米)和严重胎儿贫血及胎儿水肿的超声波证据而转诊至我们的三级胎儿医学科的病例。患者接受了宫内输血和宫内射频消融术(RFA)手术治疗。手术结束后,胎儿立即出现心动过缓,随后又出现心跳骤停。通过紧急剖腹产加快了分娩。在最合适的手术环境中对胎儿进行干预后,精心策划和快速分娩降低了婴儿的风险,并取得了良好的结果。婴儿在出生后第 84 天从新生儿科出院。 胎盘大面积脉络血管瘤是一种罕见病,但如果伴有胎儿并发症,则围产期不良结局的发生率很高。宫内干预需要周密的计划和专业的手术知识,以确保改善胎儿和新生儿的预后。据我们所知,该病例是第一例因胎儿水肿而并发胎盘巨大绒毛血管瘤的射频消融术后产后成功的病例。
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来源期刊
Case Reports in Perinatal Medicine
Case Reports in Perinatal Medicine OBSTETRICS & GYNECOLOGY-
自引率
0.00%
发文量
37
期刊介绍: Case Reports in Perinatal Medicine is a double-blind peer-reviewed journal. The objective of the new journal is very similar to that of JPM. In addition to evidence-based studies, practitioners in clinical practice esteem especially exemplary reports of cases that reveal specific manifestations of diseases, its progress or its treatment. We consider case reports and series to be brief reports describing an isolated clinical case or a small number of cases. They may describe new or uncommon diagnoses, unusual outcomes or prognosis, new or infrequently used therapies and side effects of therapy not usually discovered in clinical trials. They represent the basic concept of experiences for studies on representative groups for further evidence-based research. The potential roles of case reports and case series are: Recognition and description of new diseases Detection of drug side effects (adverse or beneficial) Study of mechanisms of disease Medical education and audit Recognition of rare manifestations of disease.
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