Stroke, Vol 23, 903-907, Copyright © 1992 by American Heart Association
J Schwitter, R Agosti, P Ott, A Kalman and W Waespe
BACKGROUND AND PURPOSE: Recently, a rare syndrome that involves uniformly
the brain, inner ear, and retina in previously healthy young women has been
described. Brain biopsies and ophthalmologic examinations disclosed small
infarcts as a pathoanatomical substrate of the disease. In previous
reports, an autoimmune disorder or a coagulopathy have been suggested as
possible etiologies. CASE DESCRIPTIONS: Both patients (aged 22 and 20
years) had brain involvement with neurological and neuropsychological
deficits. Multifocal small hyperintensities were shown in magnetic
resonance imaging of the brain. Findings of cerebrospinal fluid examination
and electroencephalography were pathological in case 1 and of cerebral
angiography in case 2. Both patients had a neurosensory hearing loss and
multiple retinal branch arteriolar occlusions. Both women were on
fenfluramine before onset of the disease. In case 1, attacks recurred
during a follow-up of 34 months. At onset of the disease the 5-
hydroxyindoleacetic acid and homovanillic acid levels of the cerebrospinal
fluid were reduced; 13 months later the 5- hydroxyindoleacetic acid level
was still reduced and the homovanillic acid level was low-normal. In case
2, with the longest follow-up of 13 years, the disease was active during
only the initial 2 1/4 years. During this period a combination of oral
anticoagulant and antiplatelet agents was ineffective. CONCLUSIONS: Our
findings could not support current etiologic hypotheses. Whether changes in
5-hydroxyindoleacetic acid and homovanillic acid levels in the
cerebrospinal fluid and/or fenfluramine intake play a role in the
pathogenesis of the disease remains to be elucidated.
ARTICLES
Small infarctions of cochlear, retinal, and encephalic tissue in young women
Department of Internal Medicine, University Hospital Zurich, Switzerland.
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