BASAL GANGLIA LACUNES AND PARKINSONISM

Citation
R. Inzelberg et al., BASAL GANGLIA LACUNES AND PARKINSONISM, Neuroepidemiology, 13(3), 1994, pp. 108-112
Citations number
13
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
02515350
Volume
13
Issue
3
Year of publication
1994
Pages
108 - 112
Database
ISI
SICI code
0251-5350(1994)13:3<108:BGLAP>2.0.ZU;2-Y
Abstract
'Arteriosclerotic' parkinsonism is still a subject of debate. The aim of this study was to investigate whether parkinsonism associated with basal ganglia lacunes possesses peculiar clinical features and a clini cal course which enables its distinction from idiopathic Parkinson's d isease (IPD). 106 consecutive ambulatory patients with the clinical di agnosis of parkinsonism were referred for CT examination. Patients in whom isolated basal ganglia lacunes were found were interviewed and ex amined, and their clinical characteristics were compared to those of p atients suffering from IPD without lacunes (controls). In 20 patients, isolated basal ganglia lacunes were detected; all had risk factors fo r stroke (significantly more than controls) and 7 of them had had clin ically diagnosed strokes. The extrapyramidal disability evolved slowly in all. The clinical picture was indistinguishable from IPD in indivi dual patients. However, tremor was significantly less frequent in this group. Lower body parkinsonism was not observed. Extrapyramidal signs were frequently asymmetrical (55 %), with no consistent relationship to the side of the lacune. Asymmetrical pyramidal signs were present i n 30% of those with unilateral lacunes, always on the appropriate side . Only 1 patient was an L-dopa nonresponder. Patients with parkinsonis m associated with basal ganglia lacunes showed tremor less frequently than other IPD patients; otherwise, clinical features and course of th e disease were indistinguishable from IPD. In these cases, parkinsonis m and basal ganglia lacunes might have occurred independently of each other and tremor might have been prevented by ischemic events.