Progressive supranuclear palsy-like phenotype associated with bilateral hypoxic-ischemic striopallidal lesions

Mov Disord. 2005 Jun;20(6):755-7. doi: 10.1002/mds.20407.

Abstract

A progressive supranuclear palsy (PSP)-like syndrome due to vascular or anoxic brain insult is rare. We describe a 65-year-old man with a progressive PSP-like phenotype associated with hypoxic-ischemic bilateral striopallidal lesions, secondary to rupture of and subsequent surgery for a thoracic aortic aneurysm. After early extrapyramidal features, 10 months later he started to fall, and developed levator inhibition. A supranuclear gaze palsy for downgaze was documented 5.5 years after the insult.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Corpus Striatum / pathology*
  • Humans
  • Hypoxia-Ischemia, Brain / complications*
  • Hypoxia-Ischemia, Brain / pathology*
  • Magnetic Resonance Imaging
  • Male
  • Supranuclear Palsy, Progressive / complications*
  • Supranuclear Palsy, Progressive / pathology*