An Yoo E, Smet Elisabeth
Obstetrics and Gynecology, Westmead Hospital, Sydney, AUS.
Maternal and Fetal Medicine, Westmead Hospital, Sydney, AUS.
Cureus. 2025 Mar 28;17(3):e81377. doi: 10.7759/cureus.81377. eCollection 2025 Mar.
A case is presented of a 27-year-old woman who was referred to our Maternal Fetal Medicine Center following the detection of a multi-cystic placenta on a routine morphology scan. Ultrasound at our unit confirmed the presence of a diffusely cystic placenta and a well-grown and structurally normal fetus. The patient's placental growth factor (PlGF) level was found to be within normal limits. At 23 weeks, an enlarging hepatic cyst was identified in the fetus and was monitored through serial imaging. A multidisciplinary team was involved, including neonatal intensivists and pediatric surgeons. The patient underwent an emergency cesarean section at 30+4 weeks of gestation after presenting with preterm labor and concerns of fetal deterioration. She delivered a live-born female infant of normal birth weight. However, the neonate required immediate resuscitation with multiple blood product transfusions, likely due to complications from the known giant hepatic cysts. She was transferred to a quaternary neonatal unit for further management. Genetic testing excluded Beckwith-Wiedemann syndrome, which had been an antenatal differential. The neonate was discharged 2.5 months later after multiple drainages of her cysts, which were benign on fluid cytology. Our case highlights the complexity of placental mesenchymal dysplasia (PMD) and the importance of early multidisciplinary care to achieve the best possible outcome. The study also underlines the need for further research into the prognostic reliability of PlGF levels in PMD.
本文报告了一例27岁女性病例,该患者在常规形态学扫描中发现多囊胎盘后被转诊至我们的母胎医学中心。我们科室的超声检查证实存在弥漫性囊性胎盘以及一个生长良好且结构正常的胎儿。发现患者的胎盘生长因子(PlGF)水平在正常范围内。在孕23周时,胎儿被发现有一个不断增大的肝囊肿,并通过系列影像学检查进行监测。一个多学科团队参与其中,包括新生儿重症监护医生和小儿外科医生。该患者在出现早产且担心胎儿情况恶化后,于妊娠30 + 4周时接受了急诊剖宫产。她产下了一名出生体重正常的活产女婴。然而,由于已知的巨大肝囊肿引发的并发症,新生儿需要立即进行复苏并多次输注血液制品。她被转至四级新生儿病房进行进一步治疗。基因检测排除了曾作为产前鉴别诊断的贝克威思 - 维德曼综合征。在对囊肿进行多次引流(囊液细胞学检查显示为良性)后,新生儿在2.5个月后出院。我们的病例突出了胎盘间质性发育异常(PMD)的复杂性以及早期多学科护理对于实现最佳可能结局的重要性。该研究还强调了对PMD中PlGF水平预后可靠性进行进一步研究的必要性。