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Temporal lobe “plus” epilepsy associated with oligodendroglial hyperplasia (MOGHE)
Author(s) -
Garganis Kyriakos,
Kokkinos Vasileios,
Zountsas Basilios,
Dinopoulos Argirios,
Coras Roland,
Blümcke Ingmar
Publication year - 2019
Publication title -
acta neurologica scandinavica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.967
H-Index - 95
eISSN - 1600-0404
pISSN - 0001-6314
DOI - 10.1111/ane.13142
Subject(s) - temporal lobe , cortical dysplasia , epilepsy , epilepsy surgery , semiology , medicine , pathological , neuroimaging , hippocampal sclerosis , electroencephalography , psychology , pathology , neuroscience
Background Mild malformation of cortical dysplasia (mMCD) with oligodendroglial hyperplasia (MOGHE) is an epilepsy‐related pathologic entity highlighted in post‐surgical specimens of frontal lobe epilepsy (FLE) patients. Aims of the Study We present two temporal lobe epilepsy (TLE) cases with MOGHE and discuss clinical, neurophysiological, and neuroimaging features that may be indicative of surgical outcome. Methods We identified two cases with MOGHE out of 30 temporal lobe epilepsy (TLE) surgical patient cohort, whose pathological distribution spared the hippocampal structures. Results The TLE cases shared common features with the FLE series in terms of patient profiles, MRI findings and post‐surgical outcome. TLE plus seizure semiology combined with extratemporal scalp electroencephalographic (EEG) and electrocorticographic (ECoG) epileptiform elements at a distance from the imaging lesion were suggestive of an underlying multifocal pathology. Conclusions MOGHE pathology has to be considered in the decision‐making process for TLE epilepsy surgery when this constellation of features is met.