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. 2016 Sep 19;139(12):3151–3162. doi: 10.1093/brain/aww229

Figure 5.

Figure 5

Exploratory ultra-high resolution ex vivo MRI. Ultra-high resolution ex vivo magnetic resonance images of a sampled brain area from Case 2 reveal striking detail of CAA-related pathology. Top row: Here we show three representative microbleeds that were identified on the ultra-high resolution T2*-weighted ex vivo magnetic resonance image (voxel size 75 µm3), of which the larger one (broken arrow) was also visible at the corresponding high resolution T2*-weighted ex vivo magnetic resonance image (voxel size 200 µm3) (A). This microbleed corresponded to a recent microhaemorrhage on haematoxylin and eosin, characterized by a focal accumulation of intact erythrocytes (broken arrow; B). The hypointense lesions (arrows) that were not rated as microbleeds at high-resolution T2*-weighted ex vivo MRI, proved to be vasculopathies on haematoxylin and eosin, without parenchymal tissue injury (arrows; B, enlarged in C and D). The vasculopathy in C resembles an occluded vessel containing fibrin deposits. The vasculopathy in D resembles a microaneurysm. Bottom row: Here we show a microinfarct that was identified on microscopic examination of the serial histological sections taken from this sample (F), and retrospectively could be identified as a hyperintense lesion on the corresponding ultra-high resolution T2-weighted ex vivo magnetic resonance image (voxel size 100 µm3) (E), whereas it escaped detection at high-resolution T2-weighted ex vivo MRI (voxel size 300 µm3). Note the vessel at the centre of this microinfarct (broken arrow in F), which can be distinguished on the scan (hypointense structure within the hyperintense lesion in E).