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8B22.3 Isolated cerebral amyloid angiopathy

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Cerebral amyloid angiopathy is characterised by the progressive accumulation of amyloid protein in the walls of small-to-medium-sized arteries and arterioles predominantly located in the leptomeningeal space, the cortex, and, to a lesser extent, also in the capillaries and veins.

synonyms

• Isolated cerebral amyloid angiopathy
• CAA - [cerebral amyloid angiopathy]
• cerebrum amyloid angiopathy
• congophilic angiopathy
• Familial dementia, British type
• Familial dementia, Danish type
• Hereditary amyloid precursor protein angiopathy
• Hereditary cerebral haemorrhage with amyloidosis, Dutch type
• Hereditary cerebral haemorrhage with amyloidosis, Icelandic type
• Hereditary cystatin C amyloid angiopathy
• Sporadic amyloid angiopathy

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