Maréchal-Ross Isabella Charlotte, Siva Sashi, Mizia Karen, Pulvers Jeremy Nicholas, Turton Isabella, Moghimi Ali
Department of Obstetrics & Gynaecology, Royal North Shore Hospital, Clinical Services Building, 1 Westbourne St, St Leonards 2065, NSW, Australia.
Department of Anatomical Pathology, NSW Health Pathology, Gosford Hospital, 75 Holden St, Gosford, NSW 2250, Australia.
Case Rep Womens Health. 2025 Apr 5;46:e00708. doi: 10.1016/j.crwh.2025.e00708. eCollection 2025 Jun.
Umbilical cord hemangiomas are rare benign vascular anomalies with limited documentation in the literature. Given their association with adverse perinatal outcomes, standardised criteria for reporting and monitoring are needed. This case report presents an instance of umbilical cord hemangioma and proposes a structured framework for future documentation. A comprehensive literature review using OVID Medline and Embase identified cases of umbilical cord hemangiomas, their clinical presentations, and maternal and neonatal outcomes. A case diagnosed in the third trimester is presented, detailing antenatal surveillance, histopathological findings, and perinatal outcomes. Key parameters were analysed in the context of the literature to inform standardised reporting criteria. A 36-year-old woman (G3P2) was diagnosed with an umbilical cord hemangioma at 29 + 3 weeks gestation following a routine growth scan. Serial ultrasound scans demonstrated lesion stability until 35 + 4 weeks, prompting increased fetal surveillance. Multidisciplinary consensus favoured expectant management, leading to an uncomplicated spontaneous vaginal delivery at 39 weeks. Histopathology confirmed a cord hemangioma composed of dilated, ectatic vascular channels lined by endothelial cells. This case contributes to the growing body of evidence on umbilical cord hemangiomas by providing detailed clinical, ultrasound, and histopathological findings. Successful expectant management and favourable perinatal outcomes highlight the role of serial ultrasound surveillance. Given the rarity and potential risks of these lesions, standardised reporting is essential to improve understanding and to guide management. By proposing a set of standardised reporting criteria, this case report serves as a step toward enhancing data consistency and informing management strategies.
脐带血管瘤是一种罕见的良性血管异常,文献记载有限。鉴于其与围产期不良结局相关,需要有标准化的报告和监测标准。本病例报告展示了一例脐带血管瘤,并提出了一个用于未来记录的结构化框架。通过使用OVID Medline和Embase进行全面的文献综述,确定了脐带血管瘤的病例、临床表现以及母婴结局。本文呈现了一例在孕晚期诊断出的病例,详细介绍了产前监测、组织病理学检查结果以及围产期结局。在文献背景下分析关键参数,以制定标准化的报告标准。一名36岁女性(孕3产2)在孕29 + 3周进行常规生长扫描后被诊断为脐带血管瘤。系列超声扫描显示病变直至孕35 + 4周保持稳定,因此加强了胎儿监测。多学科共识倾向于期待治疗,最终在孕39周实现了无并发症的自然阴道分娩。组织病理学检查证实为脐带血管瘤,由内皮细胞衬里的扩张、迂曲血管通道组成。本病例通过提供详细的临床、超声和组织病理学检查结果,为有关脐带血管瘤的证据积累做出了贡献。成功的期待治疗和良好的围产期结局凸显了系列超声监测的作用。鉴于这些病变的罕见性和潜在风险,标准化报告对于增进理解和指导治疗至关重要。通过提出一套标准化报告标准,本病例报告朝着提高数据一致性和为管理策略提供依据迈出了一步。