Literature review and case report: Rare case of successful prenatal detection of Vein of Galen Malformation (VGAM)

IF 1.5 Q3 OBSTETRICS & GYNECOLOGY
Danijel Bursać , Jasminka Stipanović , Jasenka Zmijanac Partl , Dejana Lučić , Daria Hadžić , Diana Culej Bošnjak , Željko Duić
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引用次数: 0

Abstract

Vein of Galen aneurysmal malformation (VGAM) is a rare vascular anomaly originating during embryonic development, specifically between the 6th and 11th weeks of gestation. This malformation results from abnormal arteriovenous connections between primitive choroidal arteries and the median prosencephalic vein (MPV) of Markowski. Typically, the MPV regresses by the 11th week, but in VGAM, this regression is hindered, leading to persistent abnormal flow and the formation of arteriovenous shunts. We present a case of successful prenatal detection, as well as a comprehensive literature review that summarizes current knowledge, emphasizes the importance of prenatal detection, detailed imaging techniques, understanding clinical presentations, and outlines treatment options. Prenatal detection, crucial for early intervention, has become feasible through ultrasonography and MRI. Fetal MRI has emerged as the gold standard, offering detailed insights into arterial feeders, nidus presence, fistula position, venous drainage, and potential complications. The clinical presentation of VGAM varies with age, and neonates diagnosed in utero may exhibit signs of high-output cardiac failure. Early detection is critical for timely intervention, as untreated VGAMs often result in high mortality rates. Prognosis depends on the severity of heart failure, the number of arteriovenous shunts, and the presence of accompanying fetal abnormalities. Various imaging modalities, including CT angiography and digital subtraction angiography (DSA), aid in the assessment and treatment of VGAM. DSA remains the gold standard for evaluating angioarchitecture and guiding endovascular interventions. The optimal treatment for VGAM is transarterial embolization, offering significant improvements in prognosis. Surgical interventions are limited due to high morbidity and mortality. Management decisions should consider the balance between minimizing neurological damage and achieving maximum embolization effectiveness.

文献综述和病例报告:成功产前发现盖伦静脉畸形(VGAM)的罕见病例
盖伦静脉动脉瘤畸形(VGAM)是一种罕见的血管畸形,起源于胚胎发育时期,特别是妊娠第 6 到 11 周。这种畸形是原始脉络膜动脉与马科夫斯基前脑正中静脉(MPV)之间的动静脉连接异常所致。通常情况下,MPV 在第 11 周前会逐渐消退,但在 VGAM 中,这种消退会受到阻碍,导致持续的异常血流和动静脉分流的形成。我们介绍了一例成功产前检测的病例,以及一篇全面的文献综述,综述总结了当前的知识,强调了产前检测的重要性,详细介绍了成像技术,了解了临床表现,并概述了治疗方案。产前检测对早期干预至关重要,通过超声波和核磁共振成像进行产前检测已变得可行。胎儿核磁共振成像已成为黄金标准,可详细了解动脉供血、巢穴存在、瘘管位置、静脉引流和潜在并发症。VGAM 的临床表现因年龄而异,在宫内确诊的新生儿可能会表现出高输出心力衰竭的症状。早期发现对于及时干预至关重要,因为未经治疗的 VGAM 通常会导致很高的死亡率。预后取决于心衰的严重程度、动静脉分流的数量以及是否伴有胎儿畸形。包括 CT 血管造影和数字减影血管造影(DSA)在内的各种成像模式有助于 VGAM 的评估和治疗。DSA 仍是评估血管结构和指导血管内介入治疗的黄金标准。经动脉栓塞是治疗 VGAM 的最佳方法,可显著改善预后。由于发病率和死亡率较高,手术干预受到限制。管理决策应考虑最大限度减少神经损伤和实现最大栓塞效果之间的平衡。
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
CiteScore
2.20
自引率
0.00%
发文量
31
审稿时长
58 days
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