Volume 3, Issue 1 pp. 62-63
VISUAL DIAGNOSIS
Open Access

Explosive-Onset Epilepsia Partialis Continua and Chorea

Peter F. Sarnacki

Corresponding Author

Peter F. Sarnacki

Neurological Institute, Cleveland Clinic Foundation, Cleveland, Ohio, USA

Correspondence: Peter F. Sarnacki ([email protected])

Contribution: Conceptualization, ​Investigation, Writing - original draft, Methodology, Visualization, Writing - review & editing, Formal analysis, Project administration, Data curation

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Gary Hsich

Gary Hsich

Neurological Institute, Cleveland Clinic Foundation, Cleveland, Ohio, USA

Contribution: ​Investigation, Visualization, Supervision, Writing - review & editing

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Aaron Abrams

Aaron Abrams

Neurological Institute, Cleveland Clinic Foundation, Cleveland, Ohio, USA

Contribution: Conceptualization, Writing - review & editing, Visualization, Supervision

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Sumit Parikh

Sumit Parikh

Neurological Institute, Cleveland Clinic Foundation, Cleveland, Ohio, USA

Contribution: Conceptualization, Writing - review & editing, Visualization, Supervision

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First published: 20 February 2025

This 2-year-old neurodevelopmentally normal boy presented with abrupt onset of multiple leg clonic seizures with retained awareness (Video 1). Video-electroencephalography confirmed epileptic spikes and ictal onset arising from the vertex region, with an otherwise normal background. Initially controlled with levetiracetam, the seizures evolved to right leg epilepsia partialis continua (EPC). Two weeks later, he developed a hyperkinetic movement disorder reminiscent of chorea-ballismus. One week later, he exhibited developmental regression with encephalopathy, mutism, and insomnia. Anti-N-methyl-d-aspartate receptor (anti-NMDAR) antibody was positive in serum and cerebrospinal fluid, and oligoclonal bands were present. He received intravenous high-dose steroids and intravenous immune globulin and had incremental improvement. By 9 weeks from presentation he had made a remarkable recovery with almost complete symptom resolution.

A 2-year old boy with anti-NMDAR encephalitis presenting with leg clonic seizures (part 1) and later chorea-ballismus (part 2, 3).

The vast majority (95%) of children with anti-NMDAR encephalitis will develop a movement disorder, most commonly orofacial-lingual dyskinesias, but these may manifest broadly as chorea, athetosis, ballismus, dystonia, stereotypies, opisthotonus, oculogyric crisis, or bradykinesia [1]. Compared with adults, EPC and movement disorders occur more often as the initial presenting manifestation in children [2]. A diagnosis of anti-NMDAR encephalitis should be considered in young children with new-onset movement disorders and seizures (in particular, EPC), even in the absence of classically associated psychiatric or cognitive symptoms.

Author Contributions

Peter F. Sarnacki: conceptualization, investigation, writing–original draft, methodology, visualization, writing–review and editing, formal analysis, project administration, data curation. Gary Hsich: investigation, visualization, supervision, writing–review and editing. Aaron Abrams: conceptualization, writing–review and editing, visualization, supervision. Sumit Parikh: conceptualization, writing–review and editing, visualization, supervision.

Conflicts of Interest

The authors declare no conflicts of interest.

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