Recurrent hemichorea in an adolescent with systemic lupus erythematosus and previous ipsilateral cerebral infarction

Author:

Yu Ya‐Wen1ORCID,Chung Cheng‐Yu2,Chiou Yee‐Hsuan13,Fang Nai‐Wen45ORCID

Affiliation:

1. Division of Pediatric Allergy Immunology and Rheumatology, Department of Pediatrics Kaohsiung Veterans General Hospital Kaohsiung Taiwan

2. Division of Neurology, Department of Internal Medicine Kaohsiung Veterans General Hospital Kaohsiung Taiwan

3. Department of Medical Laboratory Science and Biotechnology Fooyin University Kaohsiung Taiwan

4. Division of Pediatric Nephrology, Department of Pediatrics Kaohsiung Veterans General Hospital Kaohsiung Taiwan

5. Department of Pediatrics Pingtung Veterans General Hospital Pingtung Taiwan

Abstract

AbstractSystemic lupus erythematosus (SLE) can present with movement disorders, among which chorea is closely associated with antiphospholipid (aPL) antibodies. Brain imaging results obtained in patients with chorea are generally inconsistent with the clinical manifestation of chorea; moreover, medical tests for hemichorea, which are expected to reveal distinct localization, may show negative findings. Herein, we present a case of a 15‐year‐old girl with SLE who had a history of left cerebral infarction; tests revealed elevated aPL levels, and she developed recurrent left hemichorea 2 years later. Brain magnetic resonance imaging (MRI) results revealed no acute lesions during each episode of involuntary movements, and an MRI perfusion scan failed to provide an explanation for the asymmetric presentation. Although various hypotheses have been proposed regarding the mechanism underlying the occurrence of chorea, some scenarios still remain unexplained. Further investigation on the pathophysiology of chorea in SLE may be warranted to clarify its prognosis.

Publisher

Wiley

Subject

Rheumatology

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