Evidence map›Paper›PMID 42699933›Full record

ArticleInternational journal of surgery case reports2026

Combination of stereo-electroencephalography and electrocorticography to manage mild malformation of cortical development with oligodendroglial hyperplasia and epilepsy (MOGHE): a case report.

Farzad Sina, Vahid Heidari, Helia Hemasian, Ali Zare Mehrjardi, Mahmoud Khaleghi Mehr, Armin Ariaei

Abstract readCase Reports
In one paragraph

Article in International journal of surgery case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Farzad SinaNeurology Department, Firoozgar Hospital, Iran University of Medical Sciences, Tehran, Iran.
Vahid HeidariNeurosurgery Department, Firoozgar Hospital, Iran University of Medical Sciences, Tehran, Iran.
Helia HemasianNeurology Department, Firoozgar Hospital, Iran University of Medical Sciences, Tehran, Iran.
Ali Zare MehrjardiDepartment of Pathology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Mahmoud Khaleghi MehrNeurosurgery Department, Firoozgar Hospital, Iran University of Medical Sciences, Tehran, Iran.
Armin AriaeiFiroozgar Clinical Research Development Center (FCRDC), Department of Neurology, Firoozgar University-affiliated Hospital, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Mild malformation of cortical dysplasia with oligodendroglial hyperplasia and epilepsy (MOGHE) is a rare form of cortical malformation pathologically characterized by oligodendroglial proliferation and hypomyelination. Case presentation: Herein, we describe a 25-year-old patient with MOGHE in the right temporal lobe who has suffered from refractory epilepsy since 4 months of age, highlighting a remarkably delayed diagnosis. Magnetic resonance imaging (MRI) suggested cortical thickening and an abnormally low gyrification index in the frontotemporal region. A positron emission tomography (PET) scan reported right mesial temporal hypometabolism. The EEG findings revealed bilateral paroxysms of high-amplitude slow spike-waves with a frequency of 2.5-3 per second in the awake state and 1-1.5 per second in sleep, with a normal posterior dominant rhythm. The SEEG depicted involvement of the middle and inferior frontal gyri, temporal pole, medial temporal, and orbitofrontal regions, reflecting more extensive epileptogenic areas. Epilepsy surgery was performed to resect the right temporal lobe and portions of the frontal lobe. Pathology confirmed the presence of glial hyperplasia and abnormal neural migration. After 14 months, only occasional minor focal seizures were observed. Discussion: Temporal MOGHE lesions have previously been reported; however, in those cases, ictal patterns were limited to the lesion because of early diagnosis. In our case, delayed diagnosis resulted in the development of epileptogenic areas. Conclusion: In patients with delayed diagnosis, brain areas with a high epileptogenic index may be discordant with the locations of MRI hallmarks of MOGHE. It is hypothesized that a larger resection may help decrease seizure frequency. However, additional large-sample studies are needed to confirm this.

Indexed as

cortical malformationepilepsyoligodendroglial hyperplasiasurgery

Identifiers

PMID42699933
PMCPMC13544837

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.