| Literature DB >> 29276561 |
Meghan Romba1, Yujie Wang1, Shu-Ching Hu1, Sandeep Khot1.
Abstract
Dystonia as a manifestation of neuropsychiatric lupus erythematosus (NPSLE) is uncommon. We report a 25-year-old woman who experienced progressive confusion, reduced speech, and difficulty opening her mouth approximately 2 weeks after development of a facial rash. Brain imaging showed bilateral, symmetric signal abnormalities within the basal ganglia and subcortical white matter. Despite treatment with high-dose steroids, she continued to have difficulty speaking with evidence of jaw dystonia on examination. Jaw dystonia rapidly improved with the initiation of levodopa. Repeat evaluation 3 months later exhibited the absence of jaw dystonia and near resolution of the imaging abnormalities. Our patient demonstrated a unique presentation with jaw dystonia refractory to traditional treatment for NPSLE. Such a presentation likely represents a severe variant of NPSLE requiring both immunosuppressive and symptomatic therapies.Entities:
Keywords: clinical specialty; dystonic disorders; imaging techniques; movement disorders; neuroimmunology; parkinsonian disorders
Year: 2017 PMID: 29276561 PMCID: PMC5734500 DOI: 10.1177/1941874417698323
Source DB: PubMed Journal: Neurohospitalist ISSN: 1941-8744