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Severe cerebral amyloid angiopathy related inflammation (CAA-ri) associated with vaccination: Case report and literature review.
Tang, Michael; Kim, Jane; Lau, Kui Kai; Chan, Koon Ho.
Affiliation
  • Tang M; Division of Neurology, Department of Medicine, Queen Mary Hospital, Hong Kong Special Administrative Region; Division of Rehabilitation, Department of Medicine, Tung Wah Hospital, Hong Kong Special Administrative Region. Electronic address: michaeltang64@gmail.com.
  • Kim J; Department of Radiology and Biomedical Imaging, University of California, San Francisco, United States of America.
  • Lau KK; Division of Neurology, Department of Medicine, Queen Mary Hospital, Hong Kong Special Administrative Region.
  • Chan KH; Division of Neurology, Department of Medicine, Queen Mary Hospital, Hong Kong Special Administrative Region.
J Neuroimmunol ; 394: 578406, 2024 Jul 23.
Article in En | MEDLINE | ID: mdl-39094435
ABSTRACT
Cerebral amyloid angiopathy-related inflammation (CAA-ri) is a rapid but reversible autoimmune encephalopathy where spontaneous autoantibody reaction against amyloid beta deposited in cerebral blood vessels produces characteristic neuroinflammatory changes such as vasogenic edema and microhemorrhages on MRI. The term amyloid-related imaging abnormalities (ARIA) is sometimes used to describe these changes but are more often reserved for similar MRI signal abnormalities seen after administration of anti-amyloid immunotherapy, using treatment exposure as an antecedent. It is unclear if there is any biological basis for this dichotomized distinction. We report a case of severe CAA-ri after exposure to SARS-CoV-2 vaccine and performed a literature review of CAA-ri related to vaccination. CAA-ri precipitated by immunogenic triggers other than anti-amyloid therapy would lend support to the hypothesis that ARIA seen on MRI may represent the same disease underpinned by a shared anti-Aß autoantibody response irrespective of etiology. A thorough history should be taken before labelling CAA-ri as spontaneous.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Neuroimmunol Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Neuroimmunol Year: 2024 Document type: Article