PURPOSE: To study MR patterns of venous sinus occlusive disease and to
relate them to the underlying pathophysiology by comparing the appear
ance and pathophysiologic features of venous sinus occlusive disease w
ith those of arterial ischemic disease. METHODS: The clinical data and
MR examinations of 26 patients with venous sinus occlusive disease we
re retrospectively reviewed with special attention to mass effect, hem
orrhage, and T2-weighted image abnormalities as well as to abnormal pa
renchymal, venous, or arterial enhancement after intravenous gadopente
tate dimeglumine administration. Follow-up studies when available were
evaluated for atrophy, infarction, chronic mass effect, and hemorrhag
e. RESULTS: Mass effect was present in 25 of 26 patients. Eleven of th
e 26 had mass effect without abnormal signal on T2-weighted images. Fi
fteen patients had abnormal signal on T2-weighted images, but this was
much less extensive than the degree of brain swelling in all cases. N
o patient showed abnormal parenchymal or arterial enhancement. Abnorma
l venous enhancement was seen in 10 of 13 patients who had contrast-en
hanced studies. Intraparenchymal hemorrhage was seen in nine patients
with high signal on T2-weighted images predominantly peripheral to the
hematoma in eight. Three overall MR patterns were observed in acute s
inus thrombosis: 1) mass effect without associated abnormal signal on
T2-weighted images, 2) mass effect with associated abnormal signal on
T2-weighted images and/or ventricular dilatation that may be reversibl
e, and 3) intraparenchymal hematoma with surrounding edema. CONCLUSION
: MR findings of venous sinus occlusive disease are different from tho
se of arterial ischemia and may reflect different underlying pathophys
iology. In venous sinus occlusive disease, the breakdown of the blood-
brain barrier (vasogenic edema and abnormal parenchymal enhancement) d
oes not always occur, and brain swelling can persist up to 2 years wit
h or without abnormal signal on T2-weighted images. Abnormal signal on
T2-weighted images may be reversible and does not always indicate inf
arction.