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Pearls & Oy-sters: Arteriovenous Malformation With Sinus Thrombosis and Thalamic Hemorrhage: Unusual Cause of Parkinsonism and Dementia.

Authors :
Armenteros PR
Kapetanovic S
Lopez SG
Vazquez-Lorenzo E
Mendez LA
Gomez Muga JJ
Morales Deza ES
Iriarte ME
Garcia-Monco JC
Source :
Neurology [Neurology] 2022 Mar 29; Vol. 98 (13), pp. 550-553. Date of Electronic Publication: 2022 Feb 04.
Publication Year :
2022

Abstract

Deep cerebral venous thrombosis is an uncommon condition, which usually produces headache, altered consciousness, and ocular movement abnormality. Parkinsonism occasionally occurs when there is basal ganglia involvement. We report a case of a 78-year-old man who presented with a rapidly progressive parkinsonism with poor response to dopaminergic therapy. The patient had bilateral and symmetrical hypokinesia, rigidity, and marked gait impairment with festination. Brain MRI showed bilateral thalamic hyperintensity on T2-weighted and FLAIR sequences, with right thalamic and intraventricular hemorrhage due to straight sinus thrombosis. Angiography revealed an arteriovenous malformation in the quadrigeminal cistern with afferent supply from the posterior cerebral arteries, as well as partial thrombosis of the vein of Galen and half of the straight sinus. No predisposing factor for thrombosis was found. Given the location and size of the malformation, and the substantial amount of thalamic and intraventricular hemorrhage, conservative management was decided, with slow but progressive gait improvement. The presence of deep cerebral venous thrombosis should be suspected in cases of rapidly progressive parkinsonism with cognitive decline. As in this case, thrombosis may be secondary to a deep arteriovenous malformation, a very rare occurrence that may require specific therapy.<br /> (© 2022 American Academy of Neurology.)

Details

Language :
English
ISSN :
1526-632X
Volume :
98
Issue :
13
Database :
MEDLINE
Journal :
Neurology
Publication Type :
Academic Journal
Accession number :
35121672
Full Text :
https://doi.org/10.1212/WNL.0000000000200016