Cerebral amyloid angiopathy
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Cerebral amyloid angiopathy | |
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Synonyms | CAA |
Pronounce | N/A |
Specialty | N/A |
Symptoms | Headache, seizures, stroke, dementia |
Complications | Intracerebral hemorrhage, cognitive impairment |
Onset | Typically in older adults |
Duration | Chronic |
Types | N/A |
Causes | Deposition of amyloid beta in the walls of the blood vessels of the central nervous system |
Risks | Age, genetic factors, hypertension |
Diagnosis | MRI, CT scan, biopsy |
Differential diagnosis | Alzheimer's disease, vascular dementia, primary angiitis of the central nervous system |
Prevention | N/A |
Treatment | Supportive care, antihypertensive therapy, anticoagulation (with caution) |
Medication | N/A |
Prognosis | Variable, depends on severity and complications |
Frequency | Common in the elderly |
Deaths | N/A |
Cerebral amyloid angiopathy (CAA) is a neurological condition characterized by the accumulation of amyloid proteins in the walls of the blood vessels in the brain. This condition is often associated with Alzheimer's disease and other neurodegenerative disorders.
Etiology[edit | edit source]
The exact cause of CAA is unknown. However, it is believed to be related to the abnormal processing of amyloid precursor protein (APP), which leads to the accumulation of amyloid proteins in the brain's blood vessels. This process is similar to the one observed in Alzheimer's disease, where amyloid plaques accumulate in the brain tissue.
Pathophysiology[edit | edit source]
In CAA, amyloid proteins accumulate in the walls of the small to medium-sized blood vessels in the brain, leading to vessel wall thickening and reduced blood flow. This can result in microbleeds, microinfarcts, and, in severe cases, intracerebral hemorrhage. The most commonly involved protein is amyloid beta, the same protein involved in the formation of amyloid plaques in Alzheimer's disease.
Clinical Presentation[edit | edit source]
The clinical presentation of CAA can vary widely. Some individuals may remain asymptomatic, while others may present with cognitive impairment, dementia, stroke, or intracerebral hemorrhage. The risk of developing symptoms increases with age.
Diagnosis[edit | edit source]
Diagnosis of CAA is often challenging due to its nonspecific symptoms and the lack of definitive diagnostic tests. It is often diagnosed based on clinical presentation, neuroimaging findings, and, in some cases, brain biopsy. The Boston criteria is commonly used to diagnose CAA.
Treatment[edit | edit source]
There is currently no cure for CAA. Treatment is primarily focused on managing symptoms and preventing complications, such as stroke and intracerebral hemorrhage. This may involve the use of antihypertensive medications, anticoagulants, and statins.
Prognosis[edit | edit source]
The prognosis of CAA varies depending on the severity of the condition and the presence of complications. In severe cases, CAA can lead to significant disability and death.
See Also[edit | edit source]
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Contributors: Prab R. Tumpati, MD