Stroke, Vol 16, 1030-1038, Copyright © 1985 by American Heart Association
LR Caplan, CK Zarins and M Hemmati
Though the syndrome of carotid artery dissection is well known,
"spontaneous" vertebral artery dissection is rarely recognized. We now
report clinical and radiologic findings in five patients with presumed
vertebral dissection, one pathologically confirmed. Mean age was 35.2 years
(range 27-41). Two were men; three women. None had hypertension, vascular
disease, or trauma. Headache and neck or occipital pain was prominent in
all, often preceding other symptoms. Four of five patients had unilateral
partial alteral medullary syndromes, in one accompanied by medial medullary
signs. One patient had a cerebellar infarct. Angiography in four patients
showed severe irregular stenosis of the distal extracranial vertebral
artery (three bilaterally). A fifth patient with irregular stenosis above
the vertebral origin had verified extensive dissection in the resected
segment. No patient developed late ischemia. Repeat angiography in three
showed healing. We conclude that spontaneous vertebral artery dissection,
though rare, has recognizable clinical and radiologic features.
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Spontaneous dissection of the extracranial vertebral arteries
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