Rasmussen’s Encephalitis- Rare Epileptic Encephalopathy: A Case Report

Authors

  • Gopen Kumar Kundu Department of Paediatric Neurology, BSMMU, Dhaka
  • Rumana Islam Department of Paediatric Neurology, BSMMU, Dhaka, Bangladesh
  • SK. Serjina Anwar Department of Paediatric Neurology, BSMMU, Dhaka, Bangladesh

DOI:

https://doi.org/10.3329/bjn.v37i1.87142

Keywords:

Rasmussens encephalitis (RE), epilepsy, cortical atrophy

Abstract

Rasmussens encephalitis is a chronic progressive neurological disorder of childhood. It is a rare inflammatory disease, characterized by intractable focal epilepsy, progressive hemiplegia, cognitive deterioration, unilateral inflammation of the cerebral cortex. Median age of onset is 6 year. Our case is a 7 year old boy presented in the department of Paediatric Neurology of BSMMU with the complaints of weakness of the right side of the body, focal onset seizure, cognitive declination and difficulty of speech. In addition to classical clinical presentation of Rasmussens encephalitis, MRI brain showed hemispheric atrophy of one cerebral hemisphere.

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Published

2026-01-15

How to Cite

Kundu, G. K., Rumana Islam, & SK. Serjina Anwar. (2026). Rasmussen’s Encephalitis- Rare Epileptic Encephalopathy: A Case Report. Bangladesh Journal of Neuroscience, 37(1), 44–47. https://doi.org/10.3329/bjn.v37i1.87142

Issue

Section

Case Reports

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