Book contents
- Frontmatter
- Contents
- List of contributors
- List of abbreviations
- Preface
- Section 1 Bilateral Predominantly Symmetric Abnormalities
- Section 2 Sellar, Perisellar and Midline Lesions
- 38 Rathke's Cleft Cyst
- 39 Pituitary Microadenoma
- 40 Lymphocytic Hypophysitis
- 41 Pituitary Macroadenoma
- 42 Ectopic Posterior Pituitary Lobe
- 43 Langerhans Cell Histiocytosis
- 44 Craniopharyngioma
- 45 Hypothalamic Hamartoma
- 46 Optic Glioma
- 47 Perisellar Meningioma
- 48 Hemangioma of the Cavernous Sinus
- 49 Tolosa–Hunt Syndrome
- 50 Carotid-Cavernous Sinus Fistula
- 51 Perisellar Aneurysm
- 52 Chordoma
- 53 Chondrosarcoma
- 54 Colloid Cyst
- 55 Aqueductal Stenosis
- 56 Progressive Supranuclear Palsy (PSP)
- 57 Joubert Syndrome
- 58 Rhombencephalosynapsis
- 59 Multiple System Atrophy (MSA)
- 60 Maple Syrup Urine Disease (MSUD)
- 61 Chiari 2 Malformation
- 62 Tectal Glioma
- 63 Brainstem Glioma
- 64 Duret Hemorrhage
- 65 Hypertrophic Olivary Degeneration
- 66 Osmotic Myelinolysis
- 67 Germinoma
- 68 Pineoblastoma
- 69 Pineal Cyst
- 70 Vein of Galen Aneurysmal Malformation (VGAM)
- 71 Corpus Callosum Dysgenesis
- 72 Septo-Optic Dysplasia
- 73 Holoprosencephaly
- 74 Atretic Parietal Encephalocele
- 75 Dermoid Cyst
- 76 Lipoma
- Section 3 Parenchymal Defects or Abnormal Volume
- Section 4 Abnormalities Without Significant Mass Effect
- Section 5 Primarily Extra-Axial Focal Space-Occupying Lesions
- Section 6 Primarily Intra-Axial Masses
- Section 7 Intracranial Calcifications
- Index
- References
70 - Vein of Galen Aneurysmal Malformation (VGAM)
from Section 2 - Sellar, Perisellar and Midline Lesions
Published online by Cambridge University Press: 05 August 2013
- Frontmatter
- Contents
- List of contributors
- List of abbreviations
- Preface
- Section 1 Bilateral Predominantly Symmetric Abnormalities
- Section 2 Sellar, Perisellar and Midline Lesions
- 38 Rathke's Cleft Cyst
- 39 Pituitary Microadenoma
- 40 Lymphocytic Hypophysitis
- 41 Pituitary Macroadenoma
- 42 Ectopic Posterior Pituitary Lobe
- 43 Langerhans Cell Histiocytosis
- 44 Craniopharyngioma
- 45 Hypothalamic Hamartoma
- 46 Optic Glioma
- 47 Perisellar Meningioma
- 48 Hemangioma of the Cavernous Sinus
- 49 Tolosa–Hunt Syndrome
- 50 Carotid-Cavernous Sinus Fistula
- 51 Perisellar Aneurysm
- 52 Chordoma
- 53 Chondrosarcoma
- 54 Colloid Cyst
- 55 Aqueductal Stenosis
- 56 Progressive Supranuclear Palsy (PSP)
- 57 Joubert Syndrome
- 58 Rhombencephalosynapsis
- 59 Multiple System Atrophy (MSA)
- 60 Maple Syrup Urine Disease (MSUD)
- 61 Chiari 2 Malformation
- 62 Tectal Glioma
- 63 Brainstem Glioma
- 64 Duret Hemorrhage
- 65 Hypertrophic Olivary Degeneration
- 66 Osmotic Myelinolysis
- 67 Germinoma
- 68 Pineoblastoma
- 69 Pineal Cyst
- 70 Vein of Galen Aneurysmal Malformation (VGAM)
- 71 Corpus Callosum Dysgenesis
- 72 Septo-Optic Dysplasia
- 73 Holoprosencephaly
- 74 Atretic Parietal Encephalocele
- 75 Dermoid Cyst
- 76 Lipoma
- Section 3 Parenchymal Defects or Abnormal Volume
- Section 4 Abnormalities Without Significant Mass Effect
- Section 5 Primarily Extra-Axial Focal Space-Occupying Lesions
- Section 6 Primarily Intra-Axial Masses
- Section 7 Intracranial Calcifications
- Index
- References
Summary
Specific Imaging Findings
Prenatal ultrasound in vein of Galen aneurysmal malformation (VGAM) shows a midline cystic structure in the region of the quadrigeminal plate with intraluminal flow. Prenatal MRI shows the dilated pouch and draining sinus, hypointense on all imaging sequences due to flow phenomena. On postnatal MRI a dilated rounded to ovoid or tubular venous ampulla in the region of the quadrigeminal cistern and velum interpositum is again hypointense on all sequences, of variable, usually quite large dimensions. The arterial feeders are seen as multiple small flow-voids surrounding the ampulla; on MRA they appear to converge to the VGAM, whereas distal flow in the main cerebral arteries is not well seen. The draining vein is a persistent falcine sinus (instead of the nondeveloped straight sinus). Relative stenosis of the outflowing vein is often seen at the tentorial hiatus just below the callosal splenium. Patency of the draining vein and sinuses, especially at the sigmoid–jugular junction, must be assessed. The brain parenchyma should be carefully scrutinized for signs of injury including encephalomalacia, atrophy, subcortical calcifications, and ventriculomegaly. Herniation of cerebellar tonsils may be a consequence of venous hypertension. Catheter angiography elucidates the anatomy and pathophysiology of VGAM, but should be reserved for endovascular treatment.
Pertinent Clinical Information
Neonates with VGAM present with congestive cardiac failure – tachycardia, respiratory distress and cyanosis. During early infancy, macrocrania may appear as a consequence of maturational delay of the dural sinuses and granulations, or due to cerebral aqueduct compression by the dilated pouch, leading to hydrocephalus and intracranial hypertension. Older children usually present with chronic headache and hydrocephalus or seizures. Treatment is by transarterial embolization, and the optimal therapeutic window at 4–5 months of age has shown the best efficacy in controlling the malformation and allowing the brain to normally mature and develop. Earlier treatment carries a higher risk of failure and comorbidity; it may be contemplated in rapidly progressive cases with unresponsive heart failure. Severe diffuse brain injury is a contraindication for endovascular treatment. Spontaneous VGAM thrombosis has been described in rare cases.
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- Information
- Brain Imaging with MRI and CTAn Image Pattern Approach, pp. 143 - 144Publisher: Cambridge University PressPrint publication year: 2012