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胎儿硬脑膜窦畸形。

Malformations of the fetal dural sinuses.

作者信息

McInnes Matthew, Fong Katherine, Grin Andrea, ter Brugge Karel, Blaser Susan, Halliday William, Shannon Patrick

机构信息

Department of Medical Imaging, The Ottawa Hospital-General Campus, Ottawa, Canada.

出版信息

Can J Neurol Sci. 2009 Jan;36(1):72-7. doi: 10.1017/s031716710000634x.

Abstract

BACKGROUND

Dural sinus malformation (DSM) is a term used to describe congenital vascular malformations characterized by massive dilation of one or more dural sinuses: these dilatations are typically associated with arteriovenous shunts. Such malformations can present antenatally but their early natural history and anatomy is poorly defined.

METHODS

We reviewed five years of autopsy experience and retrieved three primary vascular malformations of the fetal dural sinuses with ultrasound, magnetic resonance imaging (MRI) and post-mortem correlation.

RESULTS

Fetal ultrasound and MRI obtained between 19 and 23 weeks gestational age demonstrated in all cases dilation of the dural sinuses. In two cases vascular thromboses were present in either the dilated dural sinus (one of three) or the associated arteriovenous fistula (one of three). All cases were autopsied at 22-23 weeks gestational age. In one there was imaging and autopsy evidence of remodeling of the dural sinuses associated with a pial arteriovenous fistula. In two cases, no arteriovenous malformation was identified on initial imaging, but only became evident at autopsy. One case showed morphological overlap with vein of Galen aneurysmal malformation, with a midline arteriovenous shunt and vein of Galen ectasia. The other demonstrated a perisylvian dural arteriovenous fistula.

CONCLUSION

In utero thrombosis of feeding vascular malformations or of the dural sinus malformation may be prominent. The early in utero developmental trajectory of dural sinus malformation (DSM) is poorly defined and deserves further study.

摘要

背景

硬脑膜窦畸形(DSM)是一个用于描述先天性血管畸形的术语,其特征是一个或多个硬脑膜窦的大量扩张:这些扩张通常与动静脉分流有关。此类畸形可在产前出现,但其早期自然病史和解剖结构尚不明确。

方法

我们回顾了五年的尸检经验,并通过超声、磁共振成像(MRI)及尸检相关性检索出三例胎儿硬脑膜窦原发性血管畸形。

结果

在孕19至23周期间获得的胎儿超声和MRI显示,所有病例均有硬脑膜窦扩张。在两例病例中,扩张的硬脑膜窦(三例中的一例)或相关动静脉瘘(三例中的一例)存在血管血栓形成。所有病例均在孕22 - 23周时进行了尸检。其中一例有影像学和尸检证据表明硬脑膜窦重塑与软脑膜动静脉瘘有关。在两例病例中,初始影像学检查未发现动静脉畸形,但仅在尸检时才明显。一例显示与大脑大静脉瘤样畸形形态重叠,有中线动静脉分流和大脑大静脉扩张。另一例显示外侧裂周围硬脑膜动静脉瘘。

结论

供血血管畸形或硬脑膜窦畸形的宫内血栓形成可能较为突出。硬脑膜窦畸形(DSM)在子宫内的早期发育轨迹尚不明确,值得进一步研究。

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