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Endovascular treatment of a pial arteriovenous fistula of a posteroinferior cerebellar artery with a double origin
  1. Leopoldo Guimaraens1,
  2. Alfredo Casasco2,
  3. Teresa Sola1,
  4. Hugo Cuellar3,
  5. Salvador Miralbes4,
  6. Francisco Jose Cambra5
  1. 1Department of Therapeutic Neuroangiography, Hospital General de Cataluña, Sant Cugat del Valles, Spain
  2. 2Department of Terapia Endovascular y Percutanea, Clínica Nuestra Señora del Rosario, Madrid, Spain
  3. 3Department of Neurosurgery, Louisiana State University Health Sciences Center, Shreveport, Louisiana, USA
  4. 4Department of Interventional Neuroradiology, Hospital Son Dureta, Palma de Mallorca, Spain
  5. 5Department of Pediatric Intensive Care Unit, Hospital Sant Joan de Deu, Barcelona, Spain
  1. Correspondence to Dr L Guimaraens, Department of Therapeutic Neuroangiography, Hospital General de Cataluña, C/Pedro i Pons, 1, 08195 Sant Cugat del Valles, Spain; guimaraens{at}mimsl.es

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.

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Footnotes

  • Competing interests None.

  • Patient consent Obtained.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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