Galen Veni anevrizmal malformasyonu nadir görülen konjenital bir malformasyondur. Tüm damarsal malformasyonların %1’ini oluşturmakla birlikte çocukluk çağında bu oran %30’a ulaşmaktadır. Yenidoğan döneminde genellikle yüksek debili kalp yetmezliği ile bulgu verir. Daha az oranda kitle etkisiyle ilerleyici nörolojik bozukluklara ve hidrosefaliye yol açabilir. Erken yenidoğan döneminde bulgu verdiğinde ölüm oranları yüksektir. Tedavi multidisipliner yaklaşım gerektirir. Günümüzdeki tedavi seçeneği endovasküler embolizasyon olup özellikle erken dönemde yapılırsa hayat kurtarıcı olabilir. Yazıda doğumdan hemen sonra kalp yetmezliği bulguları ile kliniğimizde tanı alan bir yenidoğan olgu sunuldu.
The vein of Galen aneurysmal malformation is rare congenital vascular malformation. Abnormalities of the vein of Galen account for 1% of all vascular arteriovenous malformations and around 30% of all vascular malformations in the pediatric population. It usually manifests in the newborn period with high-output cardiac failure. It can also cause mass effect leading to progressive neurological impairment and can result in hydrocephalus. The death rate is higher in those who present early in the neonatal period. The management of this condition requires a multidisciplinary approach. The current treatment of choice is endovascular embolization and can be life-saving, especially when used in the early period. The management of this condition requires a multidisciplinary approach. We report a female newborn with a vein of Galen aneurysmal malformation who presented with cardiac failure immediately after birth
Other ID | JA79BG53TU |
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Journal Section | Research Article |
Authors | |
Publication Date | December 1, 2016 |
Submission Date | December 1, 2016 |
Published in Issue | Year 2016 Volume: 10 Issue: 4 |
The publication language of Turkish Journal of Pediatric Disease is English.
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