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Table of Contents    
CASE REPORT
Year : 2019  |  Volume : 67  |  Issue : 4  |  Page : 1093-1096

Drug Refractory Epilepsy – A Series of Lesions with Triple Pathology


1 Department of Neurosurgery, Cardioneurosciences Centre, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India
2 Department of Neuropathology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India
3 Department of Neurology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India

Date of Web Publication10-Sep-2019

Correspondence Address:
Dr. Poodepedi Sarat Chandra
Department of Neurosurgery, Room No. 720, Cardioneurosciences Centre, All India Institute of Medical Sciences, Ansari Nagar, New Delhi - 110 029
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0028-3886.266289

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 » Abstract 


The associations between gangliogliomas, dysembryoplastic neuroepithelial tumors (DNETs), and cortical dysplasias remain debatable. We report five cases of drug refractory epilepsy with temporal lobe lesions. On resection, histopathological examination showed distinctive areas of gangliogliomas and DNETs with cortical dysplasia. The coexistence of the above three lesions as distinct entities in a single lesion is virtually unknown. This points to the presence of a possible etiological relationship among them. Finally, we also delve into a plausible hypothesis for such a pathogenesis.


Keywords: Cortical dysplasia, dysembryoplastic neuroepithelial tumors, gangliogliomas, triple pathology
Key Message: Gangliogliomas and Dysembryoplastic neuroepithelial tumors may be an acquired variant of cortical dysplasias. Good presurgical evaluation and complete resection using intraoperative electrocorticography is highly rewarding.


How to cite this article:
Tandon V, Chandra PS, Singla R, Bajaj J, Kakkar A, Sharma MC, Mahapatra AK, Tripathi M. Drug Refractory Epilepsy – A Series of Lesions with Triple Pathology. Neurol India 2019;67:1093-6

How to cite this URL:
Tandon V, Chandra PS, Singla R, Bajaj J, Kakkar A, Sharma MC, Mahapatra AK, Tripathi M. Drug Refractory Epilepsy – A Series of Lesions with Triple Pathology. Neurol India [serial online] 2019 [cited 2019 Nov 12];67:1093-6. Available from: http://www.neurologyindia.com/text.asp?2019/67/4/1093/266289




Daumas-Duport et al. first described dysembryoplastic neuroepithelial tumors (DNETs) in 1988.[1] These are considered benign tumors of developmental malformations and consist of a mixture of glial cell components. Gangliogliomas are low-grade tumors comprising atypical ganglion or neuronal cells and an atypical glial cell component. Cortical dysplasias can result from (i) abnormal proliferation of undifferentiated cells in the neuroepithelium; (ii) migration abnormality of neuroblasts; and (iii) anomaly of cell differentiation. Blümcke et al.[2] classified focal cortical dysplasias (FCDs) in 2011 and defined the category 3b which includes FCDs associated with tumors such as DNETs and gangliomas. These were termed as acquired processes, rather than double pathologies. Many authors have also found such associations,[3] including few reports of triple pathology like hippocampal sclerosis, FCD, and tumors.[4]

In an extensive search, we did not find any reports of coexisting FCD, a gangliogliomas, and a DNETs in a single patient. In this series, we highlight five cases where these three pathological entities coexisted in a single epileptogenic focal lesion of the temporal lobe. Their coexistence strengthens the acquired process concept. We also present our management strategy for these lesions along with a review of world literature on cases with a similar constellation of pathologies.


 » Materials and Methods Top


This study is a retrospective review of all patients with drug refractive epilepsy who have undergone surgery at our institute between January 2000 and December 2015. Cases were reviewed to confirm a diagnosis of DNETs and gangliogliomas, using criteria outlined by the World Health Organization classification of tumors.[5] Of the possible cases, five patients had coexistent DNETs, gangliogliomas, and FCD which were excised concurrently. FCDs were classified as described by Palmini et al.[6] Medical records from the hospital were reviewed and patients were followed-up with telephonically.


 » Results Top


Histopathological examinations of the five patients revealed the coexistence of a gangliogliomas, a DNETs and type I cortical dysplasia, the details of which are summarized in [Table 1]. The mean age of the patients at presentation was 26.6 years [standard deviation (SD) 10.73 years] with a mean symptom duration of 12.2 years (SD 6.94 years). The identifed semniology was of mesial temporal lobe onset. Magnetic resonance imaging (MRI) confirmed the lesions's location in the right temporal lobe in all five patients. The patients underwent right temporal corticoamygdalohippocampectomy (CAH), along with excision of these tumors. None of the patients had a recurrence of seizures during a mean follow-up period of 7 years (ranging from 2 to 15 years).
Table 1: Summary of patients with triple pathology in drug refractory epilepsy

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 » Representational Case Top


A 19-year-old man had presented with a history of sudden-onset generalized tonic clonic seizures for the past 6 years. He had no focal neurological deficit. His electroencephalogram was suggestive of few transient sharp wave activities in the right frontotemporal region leads. Contrast-enhanced MRI [Figure 1]a, [Figure 1]b, [Figure 1]c, [Figure 1]d showed a 4.5 cm × 4cm space-occupying lesion in the right temporal cortex which was of heterogeneous intensity on T1- and T2-weighted images with few areas of nodular contrast enhancement. He underwent right temporal craniotomy with electrocorticographic (ECOG)-guided gross total resection of the tumor and CAH. The tumor was intraxial (solid cystic), greyish pink and moderately vascular. The patient had an uneventful postoperative period with no recurrence of seizure.
Figure 1: Contrast enhanced MRI of a patient with axial (a and b) and sagittal (c) films showing right anteromesial temporal solid-cystic mass. (d) shows the fluid attenuated inversion recovery image with hyperintense right anteromesial temporal mass

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A histo exam revealed grossly few greyish pink brain tissues which were subjected to microscopic examination. Routine hematoxylin–eosin-stained sections showed lesion comprising areas resembling gangliogliomas. These areas consisted of an admixture of atypical-appearing astrocytic cells and focally increased numbers of atypical-appearing neuronal cells [Figure 2]a. The cells were characterized by nuclear irregularities, an abnormal distribution and amount of Nissl substance, and binucleate forms. The associated astrocytic component of the tumor was characterized by a proliferation of cells showing mild to moderate nuclear atypia, characterized by nuclear enlargement, hyperchromasia, and angularity. Mitotic figures were not identified. Vascular endothelial hyperplasia or necrosis was not seen. Numerous eosinophilic granular bodies were distributed throughout this portion of the tumor. Rare, scant perivascular lymphocytes were also identified. Calcifications were not seen.
Figure 2: Histopathological picture showing features of dysplasia, DNETs, and gangliogliomas

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Adjacent to and focally intermixed with the gangliogliomas component were morphologically distinct areas resembling DNETs. This component of the tumor was characterized by proliferation of oligodendroglial cells arranged against a microcystic background [Figure 2]b. Neurons and astrocytic cells were intermixed with the oligodendroglial component [Figure 2]c. There was no evidence of mitotic activity, vascular proliferation, necrosis, or calcifications associated with the DNETs component. No significant cytologic atypia was associated with any of the cellular components of the DNETs.

Focal areas of cortical dysplasia were seen. These areas were characterized by disorganized cortical lamination with focal neuronal cytomegaly and increased numbers of large-caliber neurons situated within cortical layers [Figure 2]c. The patient has remained free of seizure (International League Against Epilepsy (ILAE) class I) for the the past eight years following his surgery.


 » Discussion Top


A gangliogliomas, a DNETs and cortical dysplasia were identified in a single temporal lobe lesion of our patient. Such distinct occurrence is extremely rare in recent literature. Small areas of cortical dysplasia seen associated with gangliogliomas and DNETs have been described previously by Prayson [7] and Shimbo et al.[8] These are commonly reported as a “dual pathology”. Other tumors such as desmoplastic infantile gangliogliomas, angiocentric gliomas, and pleomorphic xanthoastrocytoma may occasionally be associated with FCD.[9],[10],[11] The frequent association of these three pathological entities DNETs, gangliogliomas, and cortical dysplasia suggests a common pathogenetic mechanism. Only few case reports are available, where three potentially etiological lesions are present in a patient with drug refractory epilepsy [Table 2].[17],[18],[19],[20]
Table 2: Review of literature

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Gangliogliomas and DNETs have many clinical and pathological similarities, but they are differentiated primarily on the phenotypic appearance, the atypical ganglion, or neuronal cell, and an atypical glial cell components in gangliogliomas resemble the fibrillary astrocytoma.[1] In case of a DNETs, the atypical glial cell component resembles cystic oligodendroglioma.[7] Cortical dysplasia and neuronal migration abnormalities occasionally can occur in association with DNETs and gangliogliomas.[12] Coexistence of the gangliogliomas or DNETs in patients with cortical dysplasia suggests that these lesions may be transitional forms. They also signify the tumoral form of cortical dysplasia or can occur due to neoplastic conversion of the dysplastic lesion.

Gangliogliomas have also been classified along with DNETs as dysplastic tumors indicative of the extreme end of the histopathological variety of FCD.[6] Barkovich et al. had classified DNETs as “malformations due to abnormal neuronal and glial proliferation, abnormal cell types, neoplastic, associated with disordered cortex.”[13] These also lend credit to our belief. Preoperative radiological differentiation between these three pathologies can be difficult.

A study to determine whether (11) C-methionine PET compared with (18)F-FDG PET was useful for the evaluation of FCD and mixed glioneural tumors reported that (18)F-FDG does not contribute to the differential diagnosis and that another tracer such as (11) C-methinine is required. (11) C-methinine PET results correlated well with the pathologic spectrum in pediatric lesional epilepsy patients.[14]

In these cases, preoperative planning is very important to ensure all potential epileptogenic tissue is excised. To this end, we prefer to perform ECOG-guided resections under image guidance to achieve complete resection of lesion and epileptogenic foci. The reduction of ECOG grading gives satisfaction to the operating surgeon regarding completion of the resective procedure. The authors have found excellent outcomes if epilepsy surgery approach (complete excision of the epileptogenic zone) is done.[15] All our patients had postoperative ILAE class I outcome.

Only few cases of “triple pathology” have been described. Of the seven cases reported earlier, only three cases describe a tumor (gangliogliomas) coexisting with mesial temporal sclerosis and cortical dysplasia within the same lesion.[4],[16] Yang et al. had a seizure-free outcome for 8 months despite performing a subtotal resection of the gangliogliomas, this suggests that the tumor had only a minor role in the seizure network and and that a complete excision of the hippocampal sclerosis and cortical dysplasia was mandatory.

To the best of our knowledge, this is the first series of cases which involves patients who had a DNETs, gangliogliomas, and FCD coexisting in the same lesion. These cases demonstrate the importance of accurate localization of epileptogenic activity in tumor-associated cortical dysplasias. In such cases, long-term recurrence may be dependent on completeness of the FCD excision rather than the excision of the tumor alone.


 » Conclusion Top


Gangliogliomas and DNETs can arise from the conversion of dysplastic lesion like cortical dysplasias. The coexistence of these three lesions as distinct entity in a single temporal lobe lesion is virtually unknown. An ECOG complete resection of the lesion and epileptogenic foci can provide a cure for intractable epilepsy in such patients.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
 » References Top

1.
Daumas-Duport C, Varlet P, Bacha S, Beuvon F, Cervera-Pierot P, Chodkiewicz JP. Dysembryoplastic neuroepithelial tumors: Nonspecific histological forms – A study of 40 cases. J Neurooncol1999;41:267-80.  Back to cited text no. 1
    
2.
Blümcke I, Thom M, Aronica E, Armstrong DD, Vinters HV, Palmini A, et al. The clinico-pathological spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission. Epilepsia2011;52:158-74.  Back to cited text no. 2
    
3.
Salanova V, Markand O, Worth R. Temporal lobe epilepsy: Analysis of patients with dual pathology. Acta Neurol Scand2004;109:126-31.  Back to cited text no. 3
    
4.
Yang K, Su J, Hu Z, Lang R, Sun X, Li X, et al. Triple pathology in patients with temporal lobe epilepsy: A case report and review of the literature. Exp Ther Med2013;6:925-8.  Back to cited text no. 4
    
5.
Louis DN, Perry A, Reifenberger G, von Deimling A, Figarella-Branger D, Cavenee WK, et al. The 2016 World Health Organization Classification of Tumors of the Central Nervous System: A summary. Acta Neuropathol2016;131:803-20.  Back to cited text no. 5
    
6.
Palmini A, Najm I, Avanzini G, Babb T, Guerrini R, Foldvary-Schaefer N, et al. Terminology and classification of the cortical dysplasias. Neurology2004;62 (6 Suppl 3):S2-8.  Back to cited text no. 6
    
7.
Prayson RA. Composite ganglioglioma and dysembryoplastic neuroepithelial tumor. Arch Pathol Lab Med1999;123:247-50.  Back to cited text no. 7
    
8.
Shimbo Y, Takahashi H, Hayano M, Kumagai T, Kameyama S. Temporal lobe lesion demonstrating features of dysembryoplastic neuroepithelial tumor and ganglioglioma: A transitional form? Clin Neuropathol1997;16:65-8.  Back to cited text no. 8
    
9.
Gupta K, Singla N. Desmoplastic infantile ganglioglioma with focal cortical dysplasia: A rare double pathology in an infant with history of seizures. Neuropathology2016;36:475-9.  Back to cited text no. 9
    
10.
Lach B, Duggal N, DaSilva VF, Benoit BG. Association of pleomorphic xanthoastrocytoma with cortical dysplasia and neuronal tumors. A report of three cases. Cancer1996;78:2551-63.  Back to cited text no. 10
    
11.
Marburger T, Prayson R. Angiocentric glioma: A clinicopathologic review of 5 tumors with identification of associated cortical dysplasia. Arch Pathol Lab Med 2011;135:1037-41.  Back to cited text no. 11
    
12.
Prayson RA, Khajavi K, Comair YG. Cortical architectural abnormalities and MIB1 immunoreactivity in gangliogliomas: A study of 60 patients with intracranial tumors. J Neuropathol Exp Neurol1995;54:513-20.  Back to cited text no. 12
    
13.
Barkovich AJ, Kuzniecky RI, Jackson GD, Guerrini R, Dobyns WB. A developmental and genetic classification for malformations of cortical development. Neurology2005;65:1873-87.  Back to cited text no. 13
    
14.
Phi JH, Paeng JC, Lee HS, Wang KC, Cho BK, Lee JY, et al. Evaluation of focal cortical dysplasia and mixed neuronal and glial tumors in pediatric epilepsy patients using 18F-FDG and 11C-methionine pet. J Nucl Med2010;51:728-34.  Back to cited text no. 14
    
15.
Blumcke I, Aronica E, Urbach H, Alexopoulos A, Gonzalez-Martinez JA. A neuropathology-based approach to epilepsy surgery in brain tumors and proposal for a new terminology use for long-term epilepsy-associated brain tumors. Acta Neuropathol2014;128:39-54.  Back to cited text no. 15
    
16.
Prayson RA, Gales JM. Coexistent ganglioglioma, focal cortical dysplasia, and hippocampal sclerosis (triple pathology) in chronic epilepsy. Ann Diagn Pathol2015;19:310-3.  Back to cited text no. 16
    
17.
Samura K, Morioka T, Hashiguchi K, Miyagi Y, Shigeto H, Sakata A, et al. Temporal lobe epilepsy associated with 'triple pathology' of hippocampal sclerosis, focal cortical dysplasia and cavernoma in the ipsilateral frontal lobe. Epilepsy Seizure 2009;2:34-41.  Back to cited text no. 17
    
18.
Cheong JY, Wong C, Bleasel A, Varikatt W, Ng T, Dexter MA. Late onset Rasmussen's encephalitis with triple pathology. J Clin Neurosci 2009;16:1677-81.  Back to cited text no. 18
    
19.
Maciunas JA, Syed TU, Cohen ML, Werz MA, Maciunas RJ, Koubeissi MZ. Triple pathology in epilepsy: Coexistence of cavernous angiomas and cortical dysplasias with other lesions. Epilepsy Res 2010;91:106-10.  Back to cited text no. 19
    
20.
Tong F, Jewells V, Trembath DG, Hadar E, Shin HW. Triple pathological findings in a surgically amenable patient with mesial temporal lobe epilepsy. Epilepsy Behav Case Rep 2015;4:52-5.  Back to cited text no. 20
    


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