Volume 56, Issue 8 pp. e104-e109
Brief Communication

Epilepsia partialis continua responsive to neocortical electrical stimulation

Antonio Valentin

Corresponding Author

Antonio Valentin

Department of Clinical Neurophysiology, King's College Hospital, London, United Kingdom

Department of Human Physiology, Faculty of Medicine, University Complutense, Madrid, Spain

Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology & Neuroscience (IoPPN), King's College London, London, United Kingdom

Address correspondence to Antonio Valentin, Department of Clinical Neurophysiology, King's College Hospital, Denmark Hill, London, U.K. E-mail: [email protected]Search for more papers by this author
Ismail Ughratdar

Ismail Ughratdar

Department of Neurosurgery, King's College Hospital, London, United Kingdom

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Beverly Cheserem

Beverly Cheserem

Department of Neurosurgery, King's College Hospital, London, United Kingdom

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Robert Morris

Robert Morris

Department of Neurosurgery, Addenbrookes Hospital, Cambridge, United Kingdom

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Richard Selway

Richard Selway

Department of Neurosurgery, King's College Hospital, London, United Kingdom

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Gonzalo Alarcon

Gonzalo Alarcon

Department of Clinical Neurophysiology, King's College Hospital, London, United Kingdom

Department of Human Physiology, Faculty of Medicine, University Complutense, Madrid, Spain

Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology & Neuroscience (IoPPN), King's College London, London, United Kingdom

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First published: 15 July 2015
Citations: 38

Summary

Epilepsia partialis continua (EPC), defined as a syndrome of continuous focal jerking, is a rare form of focal status epilepticus that usually affects a distal limb, and when prolonged, can produce long-lasting deficits in limb function. Substantial electrophysiologic evidence links the origin of EPC to the motor cortex; thus surgical resection carries the risk of significant handicap. We present two patients with focal, drug-resistant EPC, who were admitted for intracranial video-electroencephalography monitoring to elucidate the location of the epileptogenic focus and identification of eloquent motor cortex with functional mapping. In both cases, the focus resided at or near eloquent motor cortex and therefore precluded resective surgery. Chronic cortical stimulation delivered through subdural strips at the seizure focus (continuous stimulation at 60–130 Hz, 2–3 mA) resulted in >90% reduction in seizures and abolition of the EPC after a follow-up of 22 months in both patients. Following permanent implantation of cortical stimulators, no adverse effects were noted. EPC restarted when intensity was reduced or batteries depleted. Battery replacement restored previous improvement. This two-case report opens up avenues for the treatment of this debilitating condition.

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