Orlando Nicholas A, Mumford Kelsey, Toscano Marika, Johnson Jeremy, Gomez Erin N
Department of Radiology, Johns Hopkins University School of Medicine, 733 N Broadway, Baltimore, MD 21205, USA.
Department of Gynecology and Obstetrics, Johns Hopkins University School of Medicine, 600 North Wolfe St, Phipps 2nd floor, Baltimore, MD 21287, USA.
Radiol Case Rep. 2025 Jun 13;20(9):4373-4380. doi: 10.1016/j.radcr.2025.05.045. eCollection 2025 Sep.
Preeclampsia (PEC) spectrum disorders, including HELLP syndrome, are significant causes of maternal morbidity and mortality, affecting 2%-8% of pregnancies. While clinical signs and symptoms are pathognomonic, imaging can play a crucial role in diagnosis. We present a case of a 25-year-old primigravida at 27 weeks 4 days gestation who presented with severe upper abdominal pain and mild hypertension without other initial signs of PEC. Initial evaluation revealed early-onset fetal growth restriction with elevated umbilical artery Doppler ratios. Due to uncontrolled pain despite multimodal management, MRI was performed, revealing multiple T2 hypointense, T1 hyperintense lesions with diffusion restriction, suggesting multifocal intraplacental hematomas or villous infarcts. These findings prompted increased fetal surveillance and closer monitoring for PEC progression. Subsequently, the patient developed laboratory abnormalities consistent with PEC with severe features, including thrombocytopenia and elevated liver enzymes. Following antenatal corticosteroids and magnesium prophylaxis, she underwent urgent cesarean delivery at 28 weeks due to concerning fetal status. Histopathologic analysis confirmed features of maternal vascular malperfusion with multiple infarcts. The patient's laboratory values normalized postpartum, and she was normotensive at 6-week follow-up. This case highlights the potential role of MRI in identifying placental pathology that may precede clinical manifestations of PEC spectrum disorders, potentially allowing for earlier intervention and improved outcomes.
子痫前期(PEC)谱系障碍,包括HELLP综合征,是孕产妇发病和死亡的重要原因,影响2%-8%的妊娠。虽然临床体征和症状具有特征性,但影像学在诊断中可发挥关键作用。我们报告一例25岁初产妇,孕27周4天,出现严重上腹痛和轻度高血压,无PEC的其他初始体征。初步评估显示早期胎儿生长受限,脐动脉多普勒比值升高。尽管采取了多模式管理,但疼痛仍无法控制,遂进行了MRI检查,发现多个T2低信号、T1高信号病变,伴有弥散受限,提示多灶性胎盘内血肿或绒毛梗死。这些发现促使加强胎儿监测,并密切监测PEC的进展。随后,患者出现了与重度PEC一致的实验室异常,包括血小板减少和肝酶升高。在产前使用糖皮质激素和预防性使用镁剂后,由于胎儿状况令人担忧,她在孕28周时接受了紧急剖宫产。组织病理学分析证实了母体血管灌注不良伴多发梗死的特征。患者产后实验室检查值恢复正常,6周随访时血压正常。该病例突出了MRI在识别可能先于PEC谱系障碍临床表现的胎盘病理方面的潜在作用,可能有助于早期干预并改善结局。