Vein of Galen arteriovenous malformation mimicking coarctation of the aorta

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Vein of Galen malformation.

DESCRIPTION An 8-month-old baby boy presented to the paediatrics outpatient department with a complaint of enlargement of head size. General and cardiovascular examinations, as well as routine biochemical analysis were within normal limits. There was no evidence of skin lesions to suggest capillary malformation neither there was any limb hypertrophy, also there was no history of skin lesions, l...

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Intracranial Pial Arteriovenous Fistula Mimicking a Vein of Galen Aneurysm with Hydrocephalus Managed with Endovascular Method: Case Report

Background and Importance: Intracranial pial arteriovenous fistula is a recently described matter as a rare vascular malformation occurring in children. It is usually located in the subpial space in the intracranial cavity with a high-flow shunt. Case Presentation: Authors report on a 2-year-old child with intracranial pial arteriovenous fistula and progressive enlargement of he...

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Arteriovenous malformations involving the vein of Galen.

The vein of Galen is the largest of the deep cerebral veins formed posterior to the pineal body by confluence of the two internal cerebral veins. It curves sharply upward around the splenium of the corpus collosum and drains the deep medially located veins of the diencephalon, basal ganglia, and mid brain. Dilatation of the vein of Galen results from the force of arterial blood either directly ...

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Cerebral damage in neonates resulting from arteriovenous malformation of the vein of Galen.

Seven neonates with arteriovenous malformation of the vein of Galen are described. Six presented with cyanotic heart failure. Two cases had antenatal cerebral infarction, five periventricular leukomalacia, and three recent haemorrhagic infarction. Cerebral damage due to the malformation suggests that surgical correction of the arteriovenous malformation offers little to neonates, though after t...

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ژورنال

عنوان ژورنال: Journal of Ultrasound

سال: 2014

ISSN: 1876-7931

DOI: 10.1007/s40477-014-0080-y