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) |
|---|---|
| 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
Fingerprint
Dive into the research topics of 'Spontaneous thrombosis of developmental venous anomaly (DVA) with venous infarct and acute cerebellar ataxia'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver