Stroke, Vol 24, 132-137, Copyright © 1993 by American Heart Association
MH Huang, CC Huang, SJ Ryu and NS Chu
BACKGROUND: Bilateral hearing impairment is rare in vertebrobasilar
occlusive disease. SUMMARY OF COMMENT: Between 1986 and 1991, we
encountered seven patients (four men, three women; median age, 61 years;
range, 46-71 years) who had sudden bilateral hearing impairment among 503
patients with vertebrobasilar occlusive disease. The main initial
neurological symptoms were sudden bilateral hearing impairment, tinnitus,
and vertigo. Acute labyrinthitis or Meniere's disease was the initial
diagnosis until subsequent brain stem or cerebellar signs appeared. Brain
stem auditory evoked potentials were abnormal bilaterally in six patients
but had unilateral attenuation of the IV-V complex in the remaining one
patient. Computed tomographic scans in all six patients showed multiple
hypodense lesions in the brain stem and the cerebellum. Cerebral
angiography showed complete occlusion on both vertebral arteries in one
patient, occlusion on the left with small caliber on the right in another,
and severe stenosis on both sides in a third. There was no opacification of
internal auditory arteries in these three patients. The remaining patient
had arteriosclerotic changes with faint opacification of the bilateral
internal auditory arteries. Five patients had a poor prognosis, with
locked-in state in four and severe truncal ataxia in one. CONCLUSIONS: We
conclude that sudden bilateral hearing impairment in vertebrobasilar
occlusive disease is more common than previously recognized and that it may
indicate a grave prognosis.
ARTICLES
Sudden bilateral hearing impairment in vertebrobasilar occlusive disease
Department of Neurology, Chang Gung Memorial Hospital, Taipei, Taiwan, R.O.C.
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