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Progressive subcortical calcifications secondary to venous hypertension in an intracranial dural arteriovenous fistula
Affiliation:1. Department of Neurology, Kaohsiung Chang Gung Memorial Hospital and College of Medicine, Chang Gung University, Kaohsiung City, Taiwan;2. Department of Clinical Forensic Medicine, Kaohsiung Medical University Hospital and College of Medicine, Kaohsiung Medical University, Kaohsiung City, Taiwan;1. Department of Radiology, The Royal Melbourne Hospital, Parkville, VIC, Australia;2. Department of Radiology, The University of Melbourne, Parkville, VIC, Australia;3. Department of Cancer Imaging, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia;4. Monash Imaging, Monash Health, Clayton, VIC, Australia;1. Division of Pediatric Surgery, University of Mississippi Medical Center, 2500 North State Street, Jackson, MS 39216, USA;2. Division of Pediatric Pathology, University of Mississippi Medical Center, 2500 North State Street, Jackson, MS 39216, USA;3. Division of Pediatric Radiology, University of Mississippi Medical Center, 2500 North State Street, Jackson, MS 39216, USA;4. Division of Pediatric Gastroenterology, University of Mississippi Medical Center, 2500 North State Street, Jackson, MS 39216, USA
Abstract:Intracranial dural arteriovenous fistulas (dAVF) are acquired lesions, with the most commonly reported findings on CT haemorrhage or focal oedema. We describe a case of progressive subcortical calcification on CT secondary to venous hypertension from a high grade dAVF.
Keywords:Dural arteriovenous fistula  Subcortical calcification  Cortical venous reflux
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