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October 2000, Volume 26, Number 8, Pages 917-919
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Case Report
Rolandic encephalopathy and epilepsia partialis continua following bone marrow transplant
N L Antunes1,2, F Boulad1, V Prasad1, M Rosenblum3, E Lis4 and M Souweidane5

1Department of Pediatrics, Memorial Sloan-Kettering Cancer Center, New York, NY, USA

2Department of Neurology, Memorial Sloan-Kettering Cancer Center, New York, NY, USA

3Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, NY, USA

4Department of Radiology, Memorial Sloan-Kettering Cancer Center, New York, NY, USA

5Department of Neurosurgery, Memorial Sloan-Kettering Cancer Center, New York, NY, USA

Correspondence to: Dr N L Antunes, Department of Pediatrics, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, New York 10021, USA

Abstract

Epilepsia partialis continua (EPC) is a condition defined by prolonged focal myoclonus. Often resistant to therapy, EPC in children is frequently present in Rasmussen encephalitis, a form of chronic encephalitis of uncertain etiology. We discuss a child who developed bilateral EPC 5 months after a bone marrow transplant. Neuroimaging studies showed signal abnormalities on both sensory-motor areas. An extensive search failed to reveal the etiology of the disorder, but treatment with a broad-spectrum anti-viral agent was associated with resolution of the process. An unidentified infectious agent may be responsible for an encephalitis of the motor strip in immunosuppressed patients. Bone Marrow Transplantation (2000) 26, 917-919.

Keywords

epilepsia partialis continua; bone marrow transplant; encephalitis

Received 25 April 2000; accepted 24 July 2000
October 2000, Volume 26, Number 8, Pages 917-919
Table of contents    Previous  Abstract  Next   Full text  PDF
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