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DOI: 10.1055/s-0041-1736180
Crossed Cerebellar Diaschisis in EEG Negative Epilepsia Partialis Continua
Funding None.
Case
A 15-year-old girl, with right centroparietal focal epilepsy, presented with new onset continuous, multifocal, jerking movements of her right-sided limbs and neck (contralateral to her known epileptic focus), without electroencephalography (EEG) correlate initially. The movements were medically intractable. Magnetic resonance imaging (MRI) showed T2/fluid-attenuated inversion recovery (FLAIR) hyperintensities and restricted diffusion in the left precentral gyrus, left thalamus, and right superior cerebellum ([Fig. 1]). Whole exome sequencing revealed she was homozygous for a pathogenic variant in the POLG gene (c.1399G > A; p.A467T). POLG mutations are the most common cause of inherited mitochondrial disorders.[1] Later in the course of the admission, clear epileptiform discharges were seen arising from the left hemisphere. Seizures, including epilepsia partialis continua (EPC), are the initial clinical manifestation in 50% of cases.[1] Crossed cerebellar diaschisis (CCD), as seen in this patient with EPC, was likely a result of excessive and prolonged excitatory synaptic activity via a corticothalamic-cerebellar pathway.[2] [3] CCD has rarely been described in children, but has been previously described in children with stroke, seizures, Rasmussen's encephalitis, and hemiplegic migraine.[4] This case highlights that EEG can be unrevealing in some cases of EPC.
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Ethical Approval
The authors confirm that ethical standards have been maintained in accordance with the Declaration of Helsinki and the standards of the journal.
Author Contributions
T.L.: design and conceptualization of manuscript, drafting and revision of manuscript. S.P.: drafting and revision of manuscript.
Publication History
Received: 11 February 2021
Accepted: 26 August 2021
Article published online:
21 October 2021
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References
- 1 Rahman S, Copeland WC. POLG-related disorders and their neurological manifestations. Nat Rev Neurol 2019; 15 (01) 40-52
- 2 Graffeo CS, Snyder KA, Nasr DM, Murphy ME, Carr CM, Hocker SE. Prognostic and mechanistic factors characterizing seizure-associated crossed cerebellar diaschisis. Neurocrit Care 2016; 24 (02) 258-263
- 3 Bailly P, Bazire A, Prat G, Ben Salem D. Crossed Cerebellar Diaschisis in Status Epilepticus. Vol. 46. Paris, France: Presse Medicale; 2017
- 4 Poretti A, Boltshauser E. Crossed cerebro-cerebellar diaschisis. Neuropediatrics 2012; 43 (02) 53-54