doi: 10.3174/ajnr.A1255
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
American Journal of Neuroradiology 30:111-112, January 2009
© 2009 American Society of Neuroradiology
Case Report
INTERVENTIONAL
De Novo Cerebral Arteriovenous Malformation: Case Report and Literature Review
a Department of Radiology, Children's Hospital Medical Center, Cincinnati, Ohio
b Department of Radiology, University of Cincinnati College of Medicine, Cincinnati, Ohio
c The Neuroscience Institute, Cincinnati, Ohio
Please address correspondence to James L. Leach, MD, Cincinnati Children's Hospital Medical Center, 3333 Burnet Ave, Cincinnati, OH 45249; e-mail: james.leach{at}cchmc.org
SUMMARY: We describe a rare case of a de novo cerebral arteriovenous malformation (AVM) in a 9-year-old girl. MR imaging at 6 years of age demonstrated band heterotopia. Follow-up MR imaging 3 years later demonstrated a new 3.5-cm AVM in the left parietol-occipital region, confirmed by conventional angiography. This report, along with limited previous reports, suggests that AVMs can be acquired lesions and that AVM development is a dynamic process extending into the postnatal period.
This article has been cited by other articles:
![]() |
C A Potter, J Armstrong-Wells, H J Fullerton, W L Young, R T Higashida, C F Dowd, V V Halbach, and S W Hetts Neonatal giant pial arteriovenous malformation: genesis or rapid enlargement in the third trimester JNIS, December 1, 2009; 1(2): 151 - 153. [Abstract] [Full Text] [PDF] |
||||
