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British Journal of Radiology (2006) 79, e140-e144
© 2006 British Institute of Radiology
doi: 10.1259/bjr/44174031

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Case report

Spontaneous thrombosis of congenital cerebral arteriovenous malformation complicated by subdural collection: in utero detection with disappearance in infancy

B DeCesare, MD 2 M F Omojola, MB, FRCPC 1 E F Fogarty, MD 1 J C Brown, MD 1 and C Taylon, MD 3

Department of 1Radiology 2Creighton University Medical School3Department of Surgery, Creighton University Medical Center, Omaha, Nebraska, USA

Correspondence: Matthew F Omojola, MB, FRCPC, Associate Professor, Vice Chairman, Director of Neuroradiology, Department of Radiology, Creighton University Medical Center, 601 North 30th Street, Omaha, NE 68131, USA. E-mail: momojola{at}creighton.edu.

We report a case of congenital left temporal lobe arteriovenous malformation (AVM) detected by cranial ultrasound in utero and confirmed immediately after birth by cranial Doppler ultrasound and cranial MRI. The AVM disappeared on follow-up cranial MRI 4 months later. A small left frontal subdural collection was present on these follow-up MR images, which subsequently resolved by the 7 month MRI study. The cause of the spontaneous thrombosis of the AVM is uncertain. The frontal subdural collection may be secondary to volume loss. This case documents the perinatal presence of AVM. The baby was neurologically intact before, during and after the thrombosis of the AVM.




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J. Stevens, J.L. Leach, T. Abruzzo, and B.V. Jones
De Novo Cerebral Arteriovenous Malformation: Case Report and Literature Review
AJNR Am. J. Neuroradiol., January 1, 2009; 30(1): 111 - 112.
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