Stroke, Vol 23, 1360-1363, Copyright © 1992 by American Heart Association
W Steinke, TK Tatemichi, JP Mohr, A Massaro, I Prohovnik and RA Solomon
BACKGROUND AND PURPOSE: Caudate hemorrhage usually results from
hypertension, rupture of arteriovenous malformation or aneurysm, or rarely,
moyamoya disease. Moyamoya-like changes related to severe atherosclerotic
occlusive disease, usually causing ischemic stroke, have been reported.
CASE DESCRIPTION: A 51-year-old normotensive patient was admitted with
headache due to a left caudate hematoma with ventricular extension. There
was a history of smoking, leg claudication, elevated cholesterol, and
coronary artery disease. Angiography demonstrated complete extracranial
carotid occlusion on the left and atherosclerotic stenosis at the
bifurcation on the right, with supraophthalmic occlusion distally. At the
base of the brain, bilateral moyamoya-like vessels, presumed to be
secondary to atherosclerotic occlusion, were evident, but neither aneurysm
nor arteriovenous malformation was present. Cerebral blood flow and
transcranial Doppler studies indicated severely impaired cerebral perfusion
that improved after bilateral extracranial-to-intracranial bypass surgery.
CONCLUSIONS: Atherosclerotic occlusive carotid disease with moyamoya- like
changes may be a rare cause of caudate hemorrhage. A decrease in moyamoya
vessels with bypass surgery may reduce the risk of recurrent hemorrhage.
ARTICLES
Caudate hemorrhage with moyamoya-like vasculopathy from atherosclerotic disease
Department of Neurology, College of Physicians and Surgeons, Columbia University, New York.
This article has been cited by other articles:
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D. Chiu, P. Shedden, P. Bratina, and J. C. Grotta Clinical Features of Moyamoya Disease in the United States Stroke, July 1, 1998; 29(7): 1347 - 1351. [Abstract] [Full Text] [PDF] |
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