Paroxysmal kinesigenic dyskinesia-like phenotype in multiple sclerosis

Mult Scler. 2017 Nov;23(13):1795-1797. doi: 10.1177/1352458517702535. Epub 2017 Apr 11.

Abstract

In April 2015, a 20-year-old woman with multiple sclerosis (MS) presented with acute onset of repetitive abnormal postures and choreatic movements of the right arm, precipitated by voluntary movements (online video 1 and 2). Brain magnetic resonance imaging (MRI) showed a new active MS lesion involving the basal ganglia on the left side (Figure 1(a)). Intravenous steroid treatment resulted in rapid regression of this paroxysmal kinesigenic dyskinesia (PKD)-like hyperkinetic movement disorder. The patient became asymptomatic within 3 months. PKD is characterized by recurrent uni- or bilateral choreoathetosis and usually represents an autosomal dominant inherited disorder caused by PRRT2 gene mutations. As in the present case, a PKD-like phenotype may be associated with MS relapses in presumably genetic negative cases.

Keywords: MRI; Multiple sclerosis; basal ganglia; movement disorder.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Basal Ganglia / diagnostic imaging
  • Basal Ganglia / pathology*
  • Dyskinesias / diagnostic imaging
  • Dyskinesias / drug therapy
  • Dyskinesias / etiology*
  • Dyskinesias / physiopathology*
  • Female
  • Humans
  • Multiple Sclerosis / complications*
  • Phenotype
  • Steroids / pharmacology
  • Young Adult

Substances

  • Steroids