Epilepsy & Behavior Reports (Jan 2024)

MRI detection of mild malformation of cortical development with oligodendroglial hyperplasia (MOGHE) on T1WI-CHESS

  • Elly Arizono,
  • Zen-ichi Tanei,
  • Keiya Iijima,
  • Yukio Kimura,
  • Yoko Shigemoto,
  • Hiroyuki Maki,
  • Midori Kusama,
  • Kumiko Murayama,
  • Masaki Iwasaki,
  • Takashi Saito,
  • Yuko Saito,
  • Kazuhiro Saito,
  • Noriko Sato

Journal volume & issue
Vol. 26
p. 100674

Abstract

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Mild malformation of cortical development with oligodendroglial hyperplasia (MOGHE) is a recently proposed epileptogenic entity that is difficult to detect on MRI. We present a case of MOGHE that was successfully detected on T1WI-chemical shift-selective saturation (CHESS) MRI. The clinical presentation, MRI including T1WI-CHESS, functional images, and pathology findings of a 14-year-old Japanese girl diagnosed with MOGHE are described. T1WI-CHESS revealed an abnormal high signal along the affected lesion, whereas the findings shown by the other MR sequences were less obvious; interictal fluorodeoxyglucose-positron emission tomography indicated slightly decreased accumulation in the lesion, and subtraction ictal single photon emission computed tomography co-registered to MRI showed an increased blood flow. Together these observations suggest that T1WI-CHESS may be a useful MR sequence for detecting the lesions in patients with MOGHE.

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