Cerebral amyloid angiopathy with multifocal lobar haemorrhages
80 years old normotensive patient with right sided weakness and disturbed level of consciousness.
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Multiple left occipital as well as parietal and high posterior frontal haemorrhagic mass lesions are seen with the largest is about 3.5 X 2.5 cm. They demonstrate predominately hyperintense T1 and T2 signal with iso- to hypointense core. The lesions show blooming in GRE sequence. They show no evident post-contrast enhancement. They are surrounded by perifocal vasogenic brain oedema with some compression of the occipital horn and trigone of the left lateral ventricle. A tiny few millimeteric lesion with GRE blooming is seen in the right parietal lobe.
Mild dilatation of the ventricular system with patchy T2/FLAIR hyperintense foci at the periventricular and deep white matter.
Widened extra-axial CSF spaces; no extra-axial collection.
Normal sellar region and posterior fossa.
Mild atherosclerotic changes of the cerebral arteries with mild irregularity. Otherwise normal signal and caliber of the cerebral arteries with no occluded segment or significant stenosis.
No aneurysmal dilatation or A-V malformation.
Attenuated right vertebral artery, otherwise, normal vertebro-basilar system.
Bilateral; predominately left cerebral subacute haemorrhagic, non enhancing mass lesions; these lobar hemorrhages are suggestive of amyloid angiopathy; lack of enhancement makes haemorrhagic metastatic deposits much less likely possibility. Consider amyloid angiopathy in normotensive elderly patients with multifocal non-enhancing lobar hemorrhage.
Atrophic brain changes with periventricular arteriosclerotic leucoencephalopathy. Mild atherosclerotic changes of the cerebral arteries, with no other significant abnormality.