Abstract
Pial arteriovenous fistulas (pAVF) of the posterior fossa are rare and may present with symptoms secondary to mass effect, venous hypertension or hemorrhage, among others. A case is presented of a previously healthy 2-year-old boy with neurological deficit arising from pAVF of the posteroinferior cerebellar artery. The pAVF was successfully treated with endovascular occlusion.
| Original language | English |
|---|---|
| Pages (from-to) | 233-236 |
| Number of pages | 4 |
| Journal | Journal of NeuroInterventional Surgery |
| Volume | 3 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - Sept 2011 |
| Externally published | Yes |
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