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Published on: November 20, 2015
Intracerebral haemorrhage and cerebral amyloid angiopathy: CT features with pathological correlation
J H Miller1, J M Wardlaw, G A Lammie
1Department of Radiology, University of Edinburgh, Western General Hospital, Scotland, UK.
Insights
Computed tomography (CT) scans can reveal specific features of intracerebral hemorrhage linked to cerebral amyloid angiopathy (CAA). Recognizing these CT findings may improve in-life diagnosis of CAA, a condition often under-recognized.
Area of Science:
- Neurology
- Radiology
- Pathology
Background:
- Cerebral amyloid angiopathy (CAA) is a common cause of spontaneous intracerebral hemorrhage, particularly in the elderly.
- Accurate in-life diagnosis of CAA is challenging, often relying on post-mortem confirmation.
Purpose of the Study:
- To identify and review computed tomography (CT) features associated with pathologically confirmed cerebral amyloid angiopathy (CAA).
- To enhance the recognition of CAA during life through characteristic CT findings in patients with intracerebral hemorrhage.
Main Methods:
- Prospective collection of clinical and brain imaging records from patients with intracerebral hemorrhage and confirmed CAA post-mortem.
- Review of brain CT scans to identify common features of hemorrhage and brain pathology in affected individuals.
Main Results:
- Seven patients (aged 60-86) were studied over 30 months.
- CT findings included large, lobar hemorrhages extending to the cortex, subarachnoid space, or ventricles.
- Hemorrhages were often multiple and recurrent; blood density tended to sediment posteriorly.
Conclusions:
- Specific CT features of intracerebral hemorrhage can suggest underlying cerebral amyloid angiopathy (CAA).
- CAA associated with intracerebral hemorrhage may be under-recognized in clinical practice.
- Consideration of these CT findings could improve the in-life diagnosis of CAA.
Aims:
To review the computed tomography (CT) features of intracerebral haemorrhage pathologically proven to be associated with cerebral amyloid angiopathy in order to facilitate recognition of the presence of cerebral amyloid angiopathy in life.
Methods:
We prospectively collected the clinical and brain imaging records of patients dying following an intracerebral haemorrhage who underwent a post-mortem examination and were found to have cerebral amyloid angiopathy. We reviewed the brain imaging to highlight features of the haemorrhage and of the rest of the brain common to these cases.
Results:
Seven patients aged 60-86 years were examined over a 30-month period. On CT, the notable features were that the haemorrhages appeared large, lobar, often extended through the cortex to the subarachnoid space or into the ventricles, and were multiple and recurrent in patients who survived the initial bleed. The high density (blood) within the haematoma tended to sediment posteriorly.
Conclusions:
There are features on CT of cerebral amyloid angiopathy associated with spontaneous intracerebral haemorrhage which should raise the possibility of this underlying diagnosis. We suspect this condition is under-recognized in life, and should perhaps be considered more widely.
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