Endovascular treatment of an arteriovenous malformation associated with a double origin of the posterior inferior cerebellar artery
- ,
- Giancarlo Saal-Zapata,
- Joselyn De La Cruz
- Universidad de San Martin de Porres,
- Hospital Guillermo Almenara Irigoyen
Publication Information
Output type
Original language
EnglishPages from-to (Number of pages)
Pages 492-496 (5 pages)Journal (Volume, Issue Number)
Pediatric Neurosurgery (Volume 56, Issue 5)Publication milestones
- Published - 01/09/2021
Publication status
ISSN
1016-2291Publication IDs
- Scopus: 85111632024
- PubMed: 34237747
Abstract
Introduction: A double origin of the posterior inferior cerebellar artery (DOPICA) is a rare anatomical variant. Posterior fossa arteriovenous malformations (AVMs), especially cerebellar AVMs, are also not common. Consequently, the association of a DOPICA with a cerebellar AVM is even rare. Case Presentation: We present a rare case of a pediatric cerebellar AVM supplied by a branch of a DOPICA which was treated endovascularly with NBCA. Total obliteration was achieved in the immediate controls and at 1-year follow-up. Conclusion: Navigation through tortuous and long branches from a DOPICA is technically feasible. Although NBCA cure rates are relatively low, when the microcatheter can no longer navigate through the feeding artery, a correct dilution of NBCA with lipiodol can provide adequate penetration of this embolic agent, to obliterate the AVM nidus completely.
