Abstract
Developmental venous anomaly (DVA), formally known as venous angioma, is a congenital anatomic variant of the venous drainage of the brain. Although they typically have a benign clinical course and a low symptomatic rate, thrombosis of a drainage vein may occur, leading to potentially debilitating complications. We report a unique case of spontaneous thrombosis of a posterior fossa developmental venous anomaly with cerebellar infarct in a 61-year-old man who presented with acute onset cerebellar ataxia. DVA thrombosis was well-depicted on CT and MR studies. Patient was put on anticoagulant therapy and complete recanalization was seen on follow-up imaging.
Original language | English (US) |
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Pages (from-to) | 427-430 |
Number of pages | 4 |
Journal | Emergency Radiology |
Volume | 21 |
Issue number | 4 |
DOIs | |
State | Published - Aug 2014 |
All Science Journal Classification (ASJC) codes
- Emergency Medicine
- Radiology Nuclear Medicine and imaging