Jm. Provenzale et al., Quantitative assessment of diffusion abnormalities in posterior reversibleencephalopathy syndrome, AM J NEUROR, 22(8), 2001, pp. 1455-1461
Citations number
14
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Neurosciences & Behavoir
BACKGROUND AND PURPOSE: Previous studies have shown that lesions in posteri
or reversible encephalopathy syndrome are often isointense on diffusion-wei
ghted MR images. We hypothesized that 1) apparent diffusion coefficient (AD
C) maps using various thresholds would show larger abnormalities in posteri
or white matter (WM) and 2) isointense appearance of lesions on isotropic d
iffusion-weighted images results from a balance of T2 prolongation effects
and diffusibility effects.
METHODS: T2-weighted MR images from 11 patients were reviewed. Hyperintense
lesions were located in both anterior and posterior WM in eight patients a
nd solely in posterior WM in three patients. The ADC maps were produced by
use of ADC values greater than or equal to 3 SD and greater than or equal t
o 10 SD above the mean value of normal WM. Lesions on diffusion-weighted im
ages were classified as isointense or hypointense. ADC values within lesion
s (ADC(L)) were compared with those of normal WM (ADC(N)), and compared for
isointense lesions and hypointense lesions.
RESULTS: The distribution of lesions with ADC values greater than or equal
to 3 SD was essentially identical to that on T2-weighted images. Regions wi
th ADC values greater than or equal to 10 SD were found in both anterior WM
and posterior WM in two patients and solely in posterior WM in nine patien
ts. On diffusion-weighted images, lesions appeared isointense in seven pati
ents and hypointense in four patients. Mean ADC(L)/ADC(N) for all lesions w
as 1.81; for hypointense lesions, 2.30.
CONCLUSION. Vasogenic edema was more severe in posterior WM. Isointense les
ions result from a balance of T2 effects and increased water diffusibility.
Hypointense lesions have higher ADC values, which are not balanced by T2 e
ffects.