Stroke, Vol 16, 514-517, Copyright © 1985 by American Heart Association
MN Murphy and AA Sima
A case of cerebral amyloid angiopathy associated with granulomatous
arteritis is presented with description of the microscopic,
immunocytochemical and ultrastructural features. The amyloid proved to be
of the AL-type, with failure to show reactivity with anti-AA, anti-
prealbumin and anti-albumin. Antisera against SAP and IgG (AF) did show
reactivity. Hence the immunologic characteristics of this amyloid differ
from those of other known conditions and may therefore represent a new form
of amyloid. The role of granulomatous arteritis in this case remains
speculative.
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