Prealbumin type cerebral amyloid angiopathy in familial amyloid polyneuropathy

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Amyloid and Amyloidosis 1990

Abstract

Immunocytochemical and electron-microscopic studies were performed on the central nervous system(CNS) in 10 cases with type I familial amyloid polyneuropathy. All cases showed CNS amyloid deposits, mainly on the leptomeningeal vessels and pia-arachnoid membranes, with arteries and arterioles in subarachnoidal space being the predominant site of cerebral amyloid accumulation. All of these amyloid deposits were specifically immunolabeled by an anti-human prealbumin antibody. However, there were no prealbumin deposits in the brain parenchyma. It is concluded that CNS prealbumin-type amyloid deposition with cerebral amyloid angiopathy is a common pathological finding in this disease.

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© 1991 Springer Science+Business Media Dordrecht

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Ushiyama, M., Ikeda, Si., Yanagisawa, N. (1991). Prealbumin type cerebral amyloid angiopathy in familial amyloid polyneuropathy. In: Natvig, J.B., et al. Amyloid and Amyloidosis 1990. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-3284-8_164

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  • DOI: https://doi.org/10.1007/978-94-011-3284-8_164

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-5450-8

  • Online ISBN: 978-94-011-3284-8

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