Generic selectors
Exact matches only
Search in title
Search in content
Post Type Selectors
Search in posts
Search in pages
Filter by Categories
Book Review
Brief Report
Case Letter
Case Report
Case Series
Commentary
Current Issue
Editorial
Erratum
Guest Editorial
Images
Images in Neurology
Images in Neuroscience
Images in Neurosciences
Letter to Editor
Letter to the Editor
Letters to Editor
Letters to the Editor
Media and News
None
Notice of Retraction
Obituary
Original Article
Point of View
Position Paper
Review Article
Short Communication
Systematic Review
Systematic Review Article
Technical Note
Techniques in Neurosurgery
Generic selectors
Exact matches only
Search in title
Search in content
Post Type Selectors
Search in posts
Search in pages
Filter by Categories
Book Review
Brief Report
Case Letter
Case Report
Case Series
Commentary
Current Issue
Editorial
Erratum
Guest Editorial
Images
Images in Neurology
Images in Neuroscience
Images in Neurosciences
Letter to Editor
Letter to the Editor
Letters to Editor
Letters to the Editor
Media and News
None
Notice of Retraction
Obituary
Original Article
Point of View
Position Paper
Review Article
Short Communication
Systematic Review
Systematic Review Article
Technical Note
Techniques in Neurosurgery
Generic selectors
Exact matches only
Search in title
Search in content
Post Type Selectors
Search in posts
Search in pages
Filter by Categories
Book Review
Brief Report
Case Letter
Case Report
Case Series
Commentary
Current Issue
Editorial
Erratum
Guest Editorial
Images
Images in Neurology
Images in Neuroscience
Images in Neurosciences
Letter to Editor
Letter to the Editor
Letters to Editor
Letters to the Editor
Media and News
None
Notice of Retraction
Obituary
Original Article
Point of View
Position Paper
Review Article
Short Communication
Systematic Review
Systematic Review Article
Technical Note
Techniques in Neurosurgery
View/Download PDF

Translate this page into:

Letter to the Editor
11 (
2
); 357-358
doi:
10.1055/s-0040-1701552

An Uncommon Cause of Dysarthria in an Elderly Gentleman

Department of Neurology, Plymouth Hospital NHS Trust, Plymouth, United Kingdom
Address for correspondence Shakya Bhattacharjee, MRCP (UK) Department of Neurology, Plymouth Hospital NHS Trust Plymouth PL6 8DH United Kingdom bubai.shakya@gmail.com
Licence
This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
Disclaimer:
This article was originally published by Thieme Medical and Scientific Publishers Private Ltd. and was migrated to Scientific Scholar after the change of Publisher.

A 76-year-old gentleman presented with mild slurred speech. Five months earlier, he had vomiting and unsteady gait. Magnetic resonance imaging (MRI) head then showed hematoma of the dentate nucleus of the right cerebellum (Fig. 1, black arrow). Now the clinical examination revealed mild dysarthria, asymmetric palatal tremor predominantly involving the right palatal arch, and pharyngeal myoclonus (Video 1). The current MRI head showed hypertrophy of the contralateral inferior olivary nucleus of the medulla (Fig. 2, black arrow). He had symptomatic palatal tremor because of the contraction of the levator veli palatine muscle.1 We postulate that the pharyngeal myoclonus was due to the common vagal nerve supply. Hypertrophic olivary degeneration occurred secondary to a lesion in the Guillain–Mollaret triangle.2 The hallmark clinical feature of a lesion of the Guillain–Mollaret triangle is the palatal tremor. The unilateral palatal tremor happened due to the hypertrophic degeneration of the contralateral olivary nucleus.3 However, though bilateral symmetrical palatal tremor is common but an asymmetric bilateral tremor described in our patient was rarely reported in literature.

Fig. 1 Axial T2-weighted magnetic resonance imaging (MRI) sequence showing right cerebellar hemorrhage involving the dentate nucleus (black arrow) (dentate nucleus is a part of the Guillain–Mollaret triangle).

Fig. 1 Axial T2-weighted magnetic resonance imaging (MRI) sequence showing right cerebellar hemorrhage involving the dentate nucleus (black arrow) (dentate nucleus is a part of the Guillain–Mollaret triangle).

Fig. 2 Axial T1-weighted magnetic resonance imaging (MRI) sequence showing the hypertrophic olivary degeneration of the inferior olivary nucleus of the left hemimedullar (black arrow).

Fig. 2 Axial T1-weighted magnetic resonance imaging (MRI) sequence showing the hypertrophic olivary degeneration of the inferior olivary nucleus of the left hemimedullar (black arrow).

The palatal tremor can be essential or idiopathic and symptomatic. The essential palatal tremor occurs due to the contraction of the tensor veli palatine muscle, supplied by the trigeminal nerve.3 Often patients complain of an audible ear click. The MR head reveals no abnormalities in a patient with essential palatal tremor. Symptomatic palatal tremor occurs due to the contraction of the levator veli palatine, supplied by the vagus nerve. Many other clinical signs like Holme’s tremor, ocular tremor or flutter, or ataxia are found in patients with symptomatic palatal tremor.

Conflict of Interest

None declared.

Funding None.

References

  1. , , , . Symptomatic and essential palatal tremor. 2. Differences of palatal movements. Mov Disord. 1994;9(6):676-678.
    [Google Scholar]
  2. , , , . Hypertrophic olivary degeneration: the forgotten triangle of Guillain and Mollaret. Neurol India. 2009;57(4):507-509.
    [Google Scholar]
  3. , , . Unilateral symptomatic palatal tremor due to pontocerebellar infarction. Ann Indian Acad Neurol. 2011;14(3):219-221.
    [Google Scholar]

Fulltext Views
270

PDF downloads
117
View/Download PDF
Download Citations
BibTeX
RIS
Show Sections