Cerebral amyloid angiopathy-associated lobar intracerebral haemorrhage
Found collapsed, reduced GCS, left sided weakness and facial droop
Loading Stack -
0 images remaining
Right frontal lobar haemorrhage involving cortex, subcortical white matter and periventricular white matter. There is subarachnoid but no intraventricular or subdural haemorrhage. The haematoma has multiple finger-like projections (see stack key images).
Significant mass effect from the haematoma and perihaematomal oedema resulting in effacement of the frontal horn of the right lateral ventricle.
Moderate periventricular low attenuation in keeping with small vessel change. Mild atrophy.
Found collapsed in nursing home 3 months after the initial presentation
Loading Stack -
0 images remaining
New large acute right frontal parenchymal haemorrhage with subarachnoid haemorrhage and finger-like projections.
Interval subacute left frontal parenchymal haemorrhage.
Gliosis in the inferior right frontal lobe at the site of the previuous parenchymal haemorrhage.
Large right frontal lobar haemorrhage with the involvement of the cortex, extension into the subarachnoid spaces. The haematoma contains multiple finger-like projections. Recurrent bifrontal haemorrhages, with subarachnoid haemorrhage and finger0like projections
Lobar intracerebral haemorrhage is frequently attributed to small vessel diseases (cerebral amyloid angiopathy or arteriolosclerosis). Differentiating lobar haemorrhage due to cerebral amyloid angiopathy and arteriolosclerosis is important due to differences in recurrent ICH and post-stroke dementia risk (higher with CAA-associated ICH).
The Edinburgh CT and genetic diagnostic criteria for lobar intracerebral haemorrhage associated with cerebral amyloid angiopathy use CT features (presence of subarachnoid haemorrhage, finger-like projections arising from the ICH) and APOE e4 genotype (if available) to classify a patient as high, intermediate or low risk of CAA-associated ICH. The initial CT shows subarachnoid haemorrhage and finger-like projections from the haematoma. The patient did not possess an APOE e4 allele. Therefore they are high risk for CAA-associated ICH on the Edinburgh CT and genetic diagnostic criteria for lobar intracerebral haemorrhage associated with cerebral amyloid angiopathy.
PATHOLOGY: Postmortem performed 3 months after the initial ICH showed an extensive right cerebral haematoma with older left and right frontal haemorrhages. There is subarachnoid haemorrhage. Immunohistochemistry showed extensive vascular amyloid depositions.
The overall appearances are consistent with cerebral amyloid angiopathy-associated haemorrhage.
- Pantoni L. Cerebral small vessel disease: from pathogenesis and clinical characteristics to therapeutic challenges. (2010) The Lancet. Neurology. 9 (7): 689-701. doi:10.1016/S1474-4422(10)70104-6 - Pubmed
- Samarasekera N, Fonville A, Lerpiniere C, Farrall AJ, Wardlaw JM, White PM, Smith C, Al-Shahi Salman R. Influence of intracerebral hemorrhage location on incidence, characteristics, and outcome: population-based study. (2015) Stroke. 46 (2): 361-8. doi:10.1161/STROKEAHA.114.007953 - Pubmed
- Rodrigues MA, Samarasekera N, Lerpiniere C, Humphreys C, McCarron MO, White PM, Nicoll JAR, Sudlow CLM, Cordonnier C, Wardlaw JM, Smith C, Al-Shahi Salman R. The Edinburgh CT and genetic diagnostic criteria for lobar intracerebral haemorrhage associated with cerebral amyloid angiopathy: model development and diagnostic test accuracy study. (2018) The Lancet. Neurology. 17 (3): 232-240. doi:10.1016/S1474-4422(18)30006-1 - Pubmed
- Samarasekera N, Smith C, Al-Shahi Salman R. The association between cerebral amyloid angiopathy and intracerebral haemorrhage: systematic review and meta-analysis. (2012) Journal of neurology, neurosurgery, and psychiatry. 83 (3): 275-81. doi:10.1136/jnnp-2011-300371 - Pubmed
- Charidimou A, Gang Q, Werring DJ. Sporadic cerebral amyloid angiopathy revisited: recent insights into pathophysiology and clinical spectrum. (2012) Journal of neurology, neurosurgery, and psychiatry. 83 (2): 124-37. doi:10.1136/jnnp-2011-301308 - Pubmed