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MRI
FINDINGS IN CERVICAL DYSTONIA
Drake
D. Duane, M.D.
Arizona
Dystonia Institute/Arizona State University
Scottsdale/Tempe,
Arizona
MRI
abnormalities in cervical dystonia seem uncommon and their relationship
with the disorder unclear (Molhol and Factor. Movement Disorders.
1991;6:274-275). Retrospectively, of 212 cervical dystonia (CD)
patients evaluated per protocol between 1/88 and 1/92, 59 had head
MRI studies. Abnormalities judged by at least two evaluators as
beyond expectancy for age occurred in 28 (47%). The 21 F/10 M with
normal imaging were younger, had shorter duration of symptoms before
study and lower frequency of hypertension than the 19F/9M with abnormalities
(Mean 45Y Range (21-71) versus 54Y (26-78); 4.lY (.5-33) versus
8.2Y (.5-31); 19% versus 29%).
The
two groups were compared as to: chin direction; CD type; multichannel
EMG pattern (38 patients); extranuchal dystonic sites; neuro and
cognitive exam; mood; eye color; history of perinatal stress, migraine,
trauma, CNS infection or endocrinopathy; serologic autoimmune/endocrine
studies; response to Botox treatment; family history movement disorder.
Abnormalities
were: two with large left basal ganglia infarcts; 20 with white
matter (WM) hyperintensity--isolated left hemisphere 13, isolated
right hemisphere two (commonly internal capsule, mid- or frontal
centrum), right pontomedullary junction one; two empty sella (neither
solitary findings); one marked generalized ventricular dilatation;
four asymmetric ventricular dilatation; six age-inappropriate cortical
atrophy--one asymmetric; one isolated Arnold Chiari type 1. MRI
abnormality increased the likelihood of chin right, extranuchal
dystonic site, asymmetric neuro exam, lack of improvement with Botox
treatment.
3F/2M
had solitary focal WM T2 lesions found both < three years from
onset and before age 50. Of these five patients: four had dark eyes,
history of trauma and isolated CD; two elevated autoimmune antibody
titres; none a family hx of movement disorder. These findings suggest
further heterogeneity in the etiology, factors which may influence
the expression and/or treatment response of focal dystonia.
Poster
presentation, October 18, 1992, American Neurological Association
Pro-conference Symposia on Etiology, Pathogenesis and Prevention
of Parkinson Disease and Hyporkinetic Movement Disorders, Sponsored
by the Movement Disorder Society, Toronto, Ontario, Canada.
Duane
DD. MRI findings in cervical dystonia. Movement Disorders, Vll:
300, 1992.
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