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Review
. 2024 Mar 26:22:100306.
doi: 10.1016/j.eurox.2024.100306. eCollection 2024 Jun.

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

Affiliations
Review

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

Danijel Bursać et al. Eur J Obstet Gynecol Reprod Biol X. .

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.

Keywords: Colour Doppler; MR angiography; Prenatal diagnosis; VGAM; Vein of Galen malformation.

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Conflict of interest statement

none.

Figures

Fig. 1
Fig. 1
Colour Doppler ultrasound of transtalamic section thorugh given malformation.
Fig. 2
Fig. 2
Magnetic resonance imaging (transversal section) of transtalamic section thorugh given malformation.
Figure 3
Figure 3
Magnetic resonance imaging (sagital section) of transtalamic section thorugh given malformation.

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