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Amyloid-β (Aβ)-Related Cerebral Amyloid Angiopathy Causing Lobar Hemorrhage Decades after Childhood Neurosurgery

  • Jeremy F. Kellie
  • , Bruce C.V. Campbell
  • , Rosie Watson
  • , Adrian J. Praeger
  • , Girish Nair
  • , Anand Murugasu
  • , Christopher C. Rowe
  • , Colin L. Masters
  • , Steven Collins
  • , Catriona McLean
  • , Nawaf Yassi

Research output: Contribution to journalArticleOtherpeer-review

Abstract

Background: Recent reports raise the possibility of cerebral amyloid angiopathy (CAA) leading to intracerebral hemorrhage in young adults following childhood neurosurgery, suggesting transmission of amyloid-β (Aβ) through neurosurgical procedures including dura mater grafting. Parenchymal Aβ deposition, and to a lesser extent tau aggregation, similar to that seen in Alzheimer disease, have also been described. Methods: We conducted a database review of 634 consecutive intracerebral hemorrhage patients aged <65 years at a tertiary stroke center over 20 years to identify such patients. Results: We identified 3 patients aged in their thirties who presented with spontaneous lobar intracerebral hemorrhage, with imaging or neuropathology consistent with CAA, and a history of childhood neurosurgery. Two of these patients had undergone a dural repair using cadaveric dura mater (Lyodura). In addition to CAA, both patients had neuropathologically confirmed parenchymal Aβ and tau deposits, characteristic of Alzheimer disease. Conclusions: Our findings support the concept of neurosurgical Aβ transmission but suggest that such cases are rare in standard clinical practice.

Original languageEnglish
Pages (from-to)E369-E374
Number of pages6
JournalStroke
Volume53
Issue number8
DOIs
Publication statusPublished - 1 Aug 2022
Externally publishedYes

Keywords

  • Alzheimer disease
  • cerebral amyloid angiopathy
  • cerebral hemorrhage
  • Lyodura
  • neurosurgery

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