[Type I neurofibromatosis and megadolichobasilar artery]

Nervenarzt. 2007 Oct;78(10):1195-9. doi: 10.1007/s00115-007-2263-7.
[Article in German]

Abstract

Intracranial vascular malformations are rare but tend to appear more frequently than usual in patients with type I neurofibromatosis (NFI). Aneurysms of the basilar artery have been described four times so far. We report two cases of 51- and 62-year-old patients with type I neurofibromatosis who showed long fusiform dilation of the basilar artery. Clinically both patients presented with locked-in syndrome and died 15 and 11 days after admission. The diagnosis was confirmed by autopsy. These are the first published cases of locked-in syndrome following thrombosis of a megadolichobasilar artery in association with neurofibromatosis I. Our results show that cerebral vascular malformations are found more frequently than random chance would predict in patients with NF I.

Publication types

  • Case Reports
  • English Abstract
  • Review

MeSH terms

  • Basilar Artery / pathology
  • Brain Stem Infarctions / diagnosis
  • Brain Stem Infarctions / genetics
  • Cerebral Angiography
  • Chromosome Aberrations
  • Fatal Outcome
  • Humans
  • Intracranial Aneurysm / diagnosis*
  • Intracranial Aneurysm / genetics
  • Magnetic Resonance Angiography
  • Male
  • Middle Aged
  • Neurofibromatosis 1 / diagnosis*
  • Neurofibromatosis 1 / genetics
  • Neurologic Examination
  • Pons / pathology
  • Tomography, X-Ray Computed
  • Vertebrobasilar Insufficiency / diagnosis*
  • Vertebrobasilar Insufficiency / genetics