Hostname: page-component-586b7cd67f-l7hp2 Total loading time: 0 Render date: 2024-11-25T06:51:40.989Z Has data issue: false hasContentIssue false
  • English
  • Français

A Case of Adult Onset Tic Disorder Following Carbon Monoxide Intoxication

Published online by Cambridge University Press:  16 February 2016

Sang-Bae Ko ,
Tae-Beom Ahn ,
Jong-Min Kim ,
Yosik Kim  and
Beom S. Jeon
Sang-Bae Ko
Affiliation:
Department of Neurology, and Clinical Research Institute, Seoul National University Hospital, BK-21, Seoul
Tae-Beom Ahn
Affiliation:
Department of Neurology, and Clinical Research Institute, Seoul National University Hospital, BK-21, Seoul
Jong-Min Kim
Affiliation:
Department of Neurology, and Clinical Research Institute, Seoul National University Hospital, BK-21, Seoul
Yosik Kim
Affiliation:
Department of Neurology, Wonkwang University, Iksan, Korea
Beom S. Jeon*
Affiliation:
Neuroscience Research Institute of SNUMRC, Seoul
*
Department of Neurology, Seoul National University Hospital, Yongon-dong 28, Chongno-gu, 110-744, Seoul, Korea
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Background:

Adult onset tic disorders are usually secondary in origin. We report a case of adult onset tic disorder following carbon monoxide (CO) intoxication with typical magnetic resonance imaging features.

Case Report:

A 36-year-old woman developed temporarily suppressible patterned movements on her face, neck, and shoulder associated with sensory discomfort after CO poisoning. Magnetic resonance images showed bilateral symmetric cavitary changes in the globus pallidus. Clonazepam relieved much of her symptoms.

Conclusion:

Our patient developed a mono-symptomatic tic disorder following CO intoxication. This further supports that altered outflow signals from the basal ganglia, especially the globus pallidus, may contribute to the development of tic disorders.

Type
Case Report
Information
Canadian Journal of Neurological Sciences , Volume 31 , Issue 2 , May 2004 , pp. 268 - 270
Copyright
Copyright © The Canadian Journal of Neurological 2004

References

1.Roger, MK. Tourette’s syndrome. In: Ray, LW, William, CK, (Eds). Movement Disorders; Neurologic Principles and Practice. New York: McGraw-Hill 1997: 569–575.Google Scholar
2.Jankovic, J. Phenomenology and classification of tics. Neurol Clin 1997;15:267–275.CrossRefGoogle ScholarPubMed
3.Sylvain, C, Blair, F. Adult onset tic disorders. J Neurol Neurosurg Psychiatry 2000;68:738–743.Google Scholar
4.Yochelson, MR, David, RG. New-onset tic disorder following acute hemorrhage of an arteriovenous malformation. J Child Neurol 2000;15:769–771.CrossRefGoogle ScholarPubMed
5.Alegre, S, Chacon, J, Redondo, L, Navarro-Busto, C, Solana, B. Post-traumatic tics. Rev Neurol 1996;24:1280–1282.Google ScholarPubMed
6.Kumar, R, Lang, AE. Tourette syndrome. Secondary tic disorders. Neurologic Clin 1997;15:309–331.CrossRefGoogle ScholarPubMed
7.Pulst, SM, Walshe, TM, Romero, JA. Carbon monoxide poisoning with features of Gilles de la Tourette’s syndrome. Arch Neurol 1983;40:443–444.CrossRefGoogle ScholarPubMed
8.Klawans, HL, Stein, RW, Tanner, CM, Goetz, CG. Apure parkinsonian syndrome following acute carbon monoxide intoxication. Arch Neurol 1982;39:302–304.CrossRefGoogle Scholar
9.Davous, P, Rondot, P, Marion, MH, Gueguen, B. Severe chorea after acute carbon monoxide poisoning. J Neurol Neurosurg Psychiatry 1986;49:206–208.CrossRefGoogle ScholarPubMed
10.Schwarz, A, Hennerici, M, Wegener, OH. Delayed choreoathetosis following acute carbon monoxide poisoning. Neurology 1985;35:98–99.CrossRefGoogle Scholar
11.Choi, IS. Carbon monoxide poisoning: systemic manifestation and complication. J Korean Med Sci 2001;16:253–261.CrossRefGoogle Scholar
12.Mesiwala, AH, Loeser, JD. Bilateral globus pallidus infarction secondary to disulfiram ingestion. Pediatr Neurosurg 2001;34:224.CrossRefGoogle ScholarPubMed
13.van Wassenaer-van Hall, HN, van den Heuvel, AG, Algra, A, Hoogenraad, TU, Mali, WP. Wilson disease: findings at MR imaging and CTof the brain with clinical correlation. Radiology 1996;198:531–536.CrossRefGoogle Scholar
14.Martinez, BA, Arcas, J, Roche, MC, et al. Bilateral hypodensity of the basal ganglia. Clinico-evolutionary correlation in children. Rev Neurol 2001;33:101–111.Google Scholar
15.Abosch, A, Lozano, A. Stereotactic neurosurgery for movement disorders. Can J Neurol Sci 2003;30(Suppl 1):S72–S82.CrossRefGoogle ScholarPubMed
16.Kessler, C, Schwechheimer, K, Reuther, R, Born, JA. Hallervorden-Spatz syndrome restricted to the pallidal nuclei. J Neurol 1984;231:112–116.CrossRefGoogle Scholar
17.Peterson, BS, Riddle, MA, Cohen, DJ, et al. Reduced basal ganglia volumes in To urette’s syndrome using three-dimensional reconstruction techniques from magnetic resonance images. Neurology 1993;43:941–949.CrossRefGoogle ScholarPubMed
18.Singer, H, Reiss, A, Brown, J, et al. Volumetric MRI changes in basal ganglia of children with To urette’s syndrome. Neurology 1993;43:950–956.CrossRefGoogle ScholarPubMed
19.Eidelberg, D, Moeller, JR, Antonini, A, et al. The metabolic anatomy of Tourette’s syndrome. Neurology 1997;48:927–934.CrossRefGoogle ScholarPubMed
20.Peterson, BS. Neuroimaging studies of Tourette syndrome: a decade of progress. In: Cohen, DJ, Jankovic, J, Goetz, CG, (Eds). Tourette Syndrome. Advances in Neurology Vol 85. Philadelphia: Lippincott Williams & Wilkins, 2001;179–196.Google Scholar
21.Demirkol, A, Erdem, H, Inan, L, Yigit, A, Guney, M. Bilateral globus pallidus lesions in a patient with Tourette syndome and related disorders. Biol Psychiatry 1999:15:863–867.CrossRefGoogle Scholar