Fetal dural sinus malformation: A case report and discussion of the literature

Q3 Medicine
Jacqueline Jones, James Christie, Sarah Woodbury, Karen Mizia
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引用次数: 0

Abstract

Introduction

Fetal dural sinus malformation is a rare but important finding during pregnancy as it has the potential for significant complications.

Methods

Here we present a case of fetal dural sinus malformation and review the current literature relevant to this condition.

Results

We present the case of a 33-year-old woman who had fetal dural sinus malformation containing thrombus diagnosed at morphology ultrasound and confirmed on fetal magnetic resonance imaging (MRI). Serial ultrasounds demonstrated the sinus to reduce significantly in size over the course of the pregnancy. The woman delivered a healthy, term baby and there was no evidence of any neurological compromise in the early neonatal period.

Discussion

This case is in keeping with a recent systematic review, which identified 78 previous cases of fetal dural sinus thrombosis and reported good outcomes in most cases.

Conclusion

It therefore appears reasonable, in most cases of isolated dural sinus malformation, to monitor the progress of the lesion and continue managing the pregnancy as usual.

Abstract Image

胎儿硬脑膜窦畸形1例报告及文献讨论
胎儿硬脑膜窦畸形是一种罕见但重要的发现,在怀孕期间,因为它有潜在的显著并发症。方法本文报告1例胎儿硬脑膜窦畸形,并回顾相关文献。结果我们提出一个病例33岁的妇女谁有胎儿硬脑膜窦畸形含血栓诊断超声形态和胎儿磁共振成像(MRI)证实。连续超声显示窦在怀孕过程中明显缩小。这名妇女生下了一个健康的足月婴儿,在新生儿早期没有任何神经损伤的迹象。本病例与最近的一项系统综述一致,该综述确定了78例胎儿硬脑膜窦血栓形成,并报告了大多数病例的良好预后。结论孤立性硬脑膜窦畸形多数病例应监测病变进展,继续正常妊娠管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Australasian Journal of Ultrasound in Medicine
Australasian Journal of Ultrasound in Medicine Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
1.90
自引率
0.00%
发文量
40
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