Epilepsy and Behavior Case Reports (Jan 2017)

Functional hemispherotomy in Rasmussen syndrome in the absence of classic MRI findings

  • Yasunori Nagahama,
  • Charuta Joshi,
  • Brian Dlouhy,
  • Angela Y. Wu,
  • Taylor J. Abel,
  • Gary Baumbach,
  • Hiroto Kawasaki

DOI
https://doi.org/10.1016/j.ebcr.2016.11.003
Journal volume & issue
Vol. 7, no. C
pp. 24 – 27

Abstract

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A 7-year-old previously healthy girl presented with a left-sided focal seizure without impaired consciousness and subsequently developed epilepsia partialis continua. Initial MRI was normal, and the subsequent images only showed a focal T2/FLAIR hyperintense area without cortical atrophy. She was diagnosed with Rasmussen syndrome by pathology and promptly treated with functional hemispherotomy. Rasmussen syndrome is a rare progressive neurological disorder, the only definitive cure for which is hemispheric disconnection. The disease presents a management dilemma, especially early in disease course without characteristic neuroimaging features. A high index of suspicion, multidisciplinary approach, and clear timely communication with the family are critical.

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