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

Author:

Kellie Jeremy F.1ORCID,Campbell Bruce C.V.1ORCID,Watson Rosie23,Praeger Adrian J.4ORCID,Nair Girish4,Murugasu Anand5,Rowe Christopher C.6,Masters Colin L.7ORCID,Collins Steven27ORCID,McLean Catriona8ORCID,Yassi Nawaf13ORCID

Affiliation:

1. Departments of Medicine and Neurology, Melbourne Brain Centre at The Royal Melbourne Hospital, University of Melbourne, Australia (J.F.K., B.C.V.C., N.Y.).

2. Department of Medicine, The Royal Melbourne Hospital, University of Melbourne, Australia (R.W., S.C.).

3. Population Health and Immunity Division, The Walter and Eliza Hall Institute of Medical Research, Australia (R.W., N.Y.).

4. Department of Neurosurgery (A.J.P., G.N.), The Royal Melbourne Hospital, Australia.

5. Department of Pathology (A.M.), The Royal Melbourne Hospital, Australia.

6. Department of Molecular Imaging and Therapy, Austin Health, Australia (C.C.R.).

7. The Florey Institute of Neuroscience and Mental Health, Australia (C.L.M., S.C.).

8. Department of Anatomical Pathology, The Alfred Hospital, Australia (C.M.).

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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Advanced and Specialized Nursing,Cardiology and Cardiovascular Medicine,Neurology (clinical)

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