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新生儿因母体抗磷脂抗体经胎盘转移继发心内血栓形成——病例报告及文献复习

Neonatal intracardiac thrombosis secondary to transplacental transfer of maternal antiphospholipid antibodies-a case report and review of the literature.

作者信息

Girgulis Katherine, Skeith Leslie, Fruitman Deborah, Barber Megan, Soliman Nancy, Johnson Nicole, Steele Macgregor

机构信息

Section of Pediatric Hematology, Alberta Children's Hospital, University of Calgary, Calgary, Alberta, Canada.

Division of Hematology and Hematological Malignancies, University of Calgary, Calgary, Alberta, Canada.

出版信息

Res Pract Thromb Haemost. 2025 May 21;9(4):102895. doi: 10.1016/j.rpth.2025.102895. eCollection 2025 May.

Abstract

BACKGROUND

Maternal antiphospholipid immunoglobulin (Ig) G antibodies can cross the placenta, placing neonates at uncertain risk for thrombosis. There are no previous reports of neonatal intracardiac thrombosis (ICT) in the context of anticardiolipin antibodies (aCL).

KEY CLINICAL QUESTION

What were the clinical manifestations, management, and outcomes for a mother and her child with ICT secondary to presumed transplacental transfer of aCL?

CLINICAL APPROACH

A 2-week-old female presented with reduced feeding and was found to be poorly perfused with significant lactic acidosis. A mobile mass was noted near the left atrial appendage on the echocardiogram and confirmed on cardiac magnetic resonance imaging. Magnetic resonance imaging of the brain was normal, with no evidence of stroke. The aCL IgG titers returned highly positive for the infant (115.3 IgG phospholipid (GPL)-Unit [U]/mL) and mother (>160 GPL-U/mL; >99th percentile local reference is ≥20 GPL-U/mL). There were no other overt risk factors for thrombosis. The infant received 6 months of enoxaparin until aCL normalized. There remains a small calcified thrombus adherent to the left atrial wall. At 2 years old, the child remains healthy with no cardiac, neurologic, nor thrombotic sequelae.

CONCLUSION

This is the first report of neonatal ICT presumed secondary to maternal aCL. The outcome was favorable with anticoagulation management. Further research is needed in the area of transplacental antiphospholipid antibody transfer, identification of neonates at risk, and optimal clinical management.

摘要

背景

母体抗磷脂免疫球蛋白(Ig)G抗体可穿过胎盘,使新生儿面临不确定的血栓形成风险。此前尚无关于抗心磷脂抗体(aCL)背景下新生儿心内血栓形成(ICT)的报道。

关键临床问题

因推测aCL经胎盘转移继发ICT的母婴的临床表现、治疗及结局如何?

临床方法

一名2周大的女婴出现喂养减少,检查发现灌注不良并伴有严重乳酸酸中毒。超声心动图显示左心耳附近有一活动团块,心脏磁共振成像予以证实。脑部磁共振成像正常,无中风迹象。婴儿的aCL IgG滴度呈强阳性(115.3 IgG磷脂(GPL)单位[U]/mL),母亲的滴度也很高(>160 GPL-U/mL;当地参考值第99百分位数为≥20 GPL-U/mL)。无其他明显的血栓形成危险因素。婴儿接受了6个月的依诺肝素治疗,直至aCL恢复正常。左心房壁仍有一小片钙化血栓附着。患儿2岁时仍健康,无心脏、神经或血栓形成后遗症。

结论

这是首例推测继发于母体aCL的新生儿ICT报告。抗凝治疗后结局良好。在经胎盘抗磷脂抗体转移、识别有风险的新生儿以及优化临床管理领域,还需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26e9/12173728/6afe8d79ba6d/gr1.jpg

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