Case report - Asterixis Post High Frequency Focused-Ultrasound Thalamotomy.


Journal

Tremor and other hyperkinetic movements (New York, N.Y.)
ISSN: 2160-8288
Titre abrégé: Tremor Other Hyperkinet Mov (N Y)
Pays: England
ID NLM: 101569493

Informations de publication

Date de publication:
2022
Historique:
received: 21 07 2022
accepted: 18 08 2022
entrez: 19 9 2022
pubmed: 20 9 2022
medline: 21 9 2022
Statut: epublish

Résumé

High frequency focused ultrasound is used for treatment of essential tremor. Side effects associated with the procedure may resolve over time. We report a case of negative myoclonus, which has not been reported with this procedure. A 73-year-old left-handed man underwent focused ultrasound thalamotomy for treatment of essential tremor. Immediately post procedure he was noted to have negative myoclonus in the treated limb. This side effect resolved over the course of 6 months. Although asterixis has been associated with thalamic infarcts in the past, this has not yet been reported in the literature with MRgFUS procedure and is a novel observation. Occupational and physical therapy may be considered to address this side effect. It is important to counsel patients about the rare occurrence of this complication of therapy but also its potential for complete resolution over time.

Sections du résumé

Background
High frequency focused ultrasound is used for treatment of essential tremor. Side effects associated with the procedure may resolve over time. We report a case of negative myoclonus, which has not been reported with this procedure.
Case report
A 73-year-old left-handed man underwent focused ultrasound thalamotomy for treatment of essential tremor. Immediately post procedure he was noted to have negative myoclonus in the treated limb. This side effect resolved over the course of 6 months.
Discussion
Although asterixis has been associated with thalamic infarcts in the past, this has not yet been reported in the literature with MRgFUS procedure and is a novel observation. Occupational and physical therapy may be considered to address this side effect. It is important to counsel patients about the rare occurrence of this complication of therapy but also its potential for complete resolution over time.

Identifiants

pubmed: 36119969
doi: 10.5334/tohm.718
pmc: PMC9438457
doi:

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

26

Informations de copyright

Copyright: © 2022 The Author(s).

Déclaration de conflit d'intérêts

The authors have no competing interests to declare.

Références

Mov Disord. 2012 Oct;27(12):1567-9
pubmed: 23032792
Front Neurol. 2022 Feb 18;13:743649
pubmed: 35250802
Neurology. 2001 Feb 27;56(4):533-6
pubmed: 11222802
J Neurosurg. 2019 May 03;132(6):1785-1791
pubmed: 31051458
Case Rep Neurol Med. 2018 Jan 18;2018:3946380
pubmed: 29593921

Auteurs

Ashley Mears (A)

Rockefeller Neuroscience Institute, Morgantown, WV, US.
Department of Neurosurgery, West Virginia University, Morgantown, WV, US.

Ali R Rezai (AR)

Rockefeller Neuroscience Institute, Morgantown, WV, US.
Department of Neurosurgery, West Virginia University, Morgantown, WV, US.

Richa Tripathi (R)

Rockefeller Neuroscience Institute, Morgantown, WV, US.
Department of Neurology, West Virginia University, Morgantown, WV, US.
West Virginia Clinical and Translational Science Institute, West Virginia University, Morgantown, WV, US.

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Classifications MeSH