Stroke, Vol 18, 342-351, Copyright © 1987 by American Heart Association
LD DeWitt, JP Kistler, DC Miller, EP Richardson Jr and FS Buonanno
True, three-dimensional proton nuclear magnetic resonance imaging at 0.147
tesla was performed postmortem on 2 patients embodying various stroke
syndromes, including chronic (4 and 15 years) infarction, subacute (within
1 week) bland infarction, acute (2 days) hemorrhagic infarction, and
hematoma secondary to ruptured aneurysm. A third patient, with subcortical
arteriosclerotic encephalopathy, so-called Binswanger's disease, was
examined antemortem using a 0.6 tesla scanner. Nuclear magnetic resonance
images were reconstructed at levels matching the pathologic specimens.
Qualitative and, when available, quantitative comparisons between the
results of nuclear magnetic resonance imaging and pathology were carried
out. Areas of qualitatively prolonged T1 and T2 relaxation times on nuclear
magnetic resonance imaging were more extensive than the corresponding areas
of chronic infarction noted pathologically and were determined to be
infarcts plus the adjacent areas of Wallerian degeneration. Hemorrhagic
infarction, without evidence of blood on computed tomography, was found to
have mildly prolonged T1 and T2 relaxation times, between those of normal
brain and chronic infarction; a 10-day-old hematoma had a very short T1,
slightly shorter than that of white matter, and a mildly prolonged T2, with
values between those of white and gray matter. Subcortical arteriosclerotic
encephalopathy was found to have areas of prolonged T1 and T2 relaxation
times involving almost the entire white matter of the corona radiata.
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NMR-neuropathologic correlation in stroke
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