Department of Radiology, Boston Children's Hospital, Boston, Massachusetts, USA.
Advanced Fetal Care Center, Boston Children's Hospital, Boston, Massachusetts, USA.
J Neurointerv Surg. 2018 May;10(5):471-475. doi: 10.1136/neurintsurg-2017-013343. Epub 2017 Sep 30.
Torcular dural sinus malformations (tDSMs) are described as slow flow dural arteriovenous fistulae with frequently poor outcomes in the neuroangiographic literature, but other etiologies have been proposed in the obstetric literature, where outcomes have been more favorable.
To review tDSMs reported in the literature of multiple specialties for features that support a common etiology, and to identify key prognostic factors, with an emphasis on tDSM trajectory highlighted in part I.
Analysis of imaging features and clinical outcome for 77 prenatal and 22 postnatal tDSMs reported in 37 papers from the literature.
In addition to large venous lakes, 36% of prenatal and 96% of postnatal tDSMs had evidence of arterialization, where specifically assessed. For fetal cases, where there was an observable natural history, 97% underwent a spontaneous decrease-13% after an initial increase and only 1 case with subsequent enlargement after a decrease. Prenatal cases had 83% survival (62% with a favorable outcome) whereas postnatal cases had 59% survival (29% favorable). In addition to a postnatal diagnosis, unfavorable features included ventriculomegaly, parenchymal injury, arterialization, and need for intervention. Favorable features included decreasing tDSM size, presence of clot, and increasing clot percentage.
Neonatal and fetal tDSMs have overlapping imaging appearances, suggesting a common etiology, where neonatal tDSMs represent those rare fetal tDSMs that do not undergo spontaneous regression and have a propensity for worse outcomes. Decrease in tDSM size is a critical observation when managing a tDSM because it is generally irreversible and associated with a favorable outcome.
在神经血管造影文献中,Torcular 硬脑膜窦畸形(tDSM)被描述为缓慢血流硬脑膜动静脉瘘,通常预后较差,但在产科文献中提出了其他病因,其预后更为有利。
回顾文献中多学科报道的 tDSM 的特征,以支持共同病因,并确定关键的预后因素,重点是第一部分强调的 tDSM 轨迹。
分析 37 篇文献中报道的 77 例产前和 22 例产后 tDSM 的影像学特征和临床转归。
除了大的静脉湖外,36%的产前 tDSM 和 96%的产后 tDSM 有动脉化的证据,具体评估。对于有可观察自然史的胎儿病例,97%的病例自发性减少-13%在最初增加后,只有 1 例在减少后增大。产前病例存活率为 83%(62%预后良好),而产后病例存活率为 59%(29%预后良好)。除了产后诊断外,不良特征包括脑室扩大、实质损伤、动脉化和需要干预。有利特征包括 tDSM 大小减小、有血栓形成和血栓百分比增加。
新生儿和胎儿 tDSM 的影像学表现重叠,提示病因相同,其中新生儿 tDSM 代表那些罕见的胎儿 tDSM,不会自发消退,且预后较差。tDSM 大小减小是管理 tDSM 的关键观察,因为它通常是不可逆的,并与良好的预后相关。