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Lesional epilepsy
 Dr. M.Manoranjitha kumari
   Prof V.G.Ramesh‘s unit
Madras Institute Of Neurology
          Chennai
Case
14 yr old male, 8 th std, namakkal
c/o seizures- 5 yrs duration
HOPI: apparently normal till 5 yrs ago, one day he
  developed staring look, not responding to his
  mother call, lasting for 1 -2mnts without any
  clonic tonic movement, regained his activities
  after few minutes without any post ictal
  confusion , head ache, or weakness not
  preceeded aura. 1 episode in a month- 3 yrs.
  Started on CBZ and Levitiracetam, frequency of
  seizures increased to once in 10 days- 2 yrs.
•   For the past one month 2-3 times a day, starts as a starring
  look followed by turning of head towards left side with
  deviation of eye towards left side,with tonic posturing of left
  hand followed by right hand, some times with clonic
  movements, with loss of consciousness lasting for 1-2 mnts,
  without any post ictal confusion or weakness, with or without
  preceeding aura
•    no head ache /vomiting/behavioural disturbances/limb
  weakness/cranial nerve disturbances/trauma
• Past history: evaluated for epilepsy in 2004
     ct plain was reported as calcified glioma,
  started on AED, 2008 AED dose increased and
  ct was repeated and was reported as calcified
  granuloma
Antenatal natal post natal history, family history
  nil relevant
• O/E : pt conscious, oriented
        thin bult, no neurocutaneous marker
HMF: normal
Lobar functions: normal
Cranial nerves: normal
Sms : normal
Cerebellar function: normal
Spine and cranium: normal
CT brain
2004       2008
MRI
3.5*2.5*2.5*cm sized T1 &T2
hetero intense lesion noted in
the right superior middle
temporal gyrus with cortical
expansion. Calvarial
remodelling noted in the
adjacent right temporal lobe.
No evidence of diffusion
restriction in the cortical
lesion, minimal heterogenous
enhancement noted in the
lesion. Evidence of blooming
in GRE

D/D
  DNET
  Oligidendroglioma
  Ganglioglioma
• EEG- normal study
• Other investigations- normal
Differential diagnosis
• Oligodendroglioma
• Ganglioglioma
• DNET
Surgery
• Right temporal craniotomy, trans cortical
  approach and total excision of tumor done,
  the tumor was soft, with areas of old
  hemorrhages and calcification.
Biopsy
• Squash : tuberculoma
• HPE– suggestive of vascular tumor - angioma
Post opertative
• No fits after surgery
• On AED – dose is being taperd
Post op scan
Post op EEG
• Background shows well formed alpha waves in
  posterior head regions, responding normally
  to eye opening. Bilateral sharp waves and
  spikes seen more during hyperventilation and
  after hyperventilation. No slow waves seen.
• Imp : abnormal record suggestive of bilateral
  epileptiform avtivity
What is lesional epilepsy?
• In some patients with longstanding epilepsy
  the cause of the seizure may be a slow
  growing tumors , vascular malformations,
  infections or congenital anomalies. These
  lesions are picked up in the MRI.
• Removal of the lesion may cure a patients
  with epilepsy
Classification
•   Temporal lobe epilepsy
•   Extra temporal lobe lesional epilepsy
•   Subcortical lesional epilepsy
•   Catastrophic epilepsy
Temporal lobe and extra temporal
        lobe lesional epilepsy
• Neoplastic- eg. Astrocytoma,
  ganglioglioma,pleomorphic xanthoastrocytoma,
  DNET
• Vascular-eg. Cavernous hemangioma,
  arteriovenous malformation, angioma
• Dysgenetic -eg. Focal or diffuse cortical dysplasia,
  sturge weber syndrome, tuberous sclerosis
• Traumatic
• Ischemic
Subcortical epilepsy
• Hypothalamic hamartoma
• Cerebellar seizures
Catastrophic epilepsy
•   Hemimegalencephaly
•   Diffuse cortical dysplasias
•   Rasmussens
•   Porencephalic cyst
Long term seizure control after
           lesionectomy
9 years follow up of 53 patients operated for
supra tentorial cavernomas:
   45 (84.9%)pts- free from disabling seizure-
Engels class1
   37(69.8%)pts –completely free of post op
seizure Engels class 1A


                          International league against epilesy
                          JNS nov 2008- volume 63
• 22 out of 26 cases -84.6% of seizure control
  after surgery for temporal lobe ganglioglima
                           (Morris et al)


• Complete seizure relief in12 of16
  patients(75%) operated for DNET
                           Raymond et al
Predictors of seizure control after
                 surgery
• Lower pre op frequency of partial seizure associated with better
  outcome
• Presence of CPS – supportive predictive parameters for satisfactory
  seizure relief
• Secondary seizure generalization- negative predictor for seizure
  control
• Because of very low rate of patients with discordant EEG patterns ,
  information derived from EEG recordings is not suitable to
  discriminate patients with a lower expectation of seizure control.
• Other studies found a significant contribution of EEG data in
  predicting outcome after surgery especially in patients with mesial
  temporal sclerosis.

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Lesional epilepsy

  • 1. Lesional epilepsy Dr. M.Manoranjitha kumari Prof V.G.Ramesh‘s unit Madras Institute Of Neurology Chennai
  • 2. Case 14 yr old male, 8 th std, namakkal c/o seizures- 5 yrs duration HOPI: apparently normal till 5 yrs ago, one day he developed staring look, not responding to his mother call, lasting for 1 -2mnts without any clonic tonic movement, regained his activities after few minutes without any post ictal confusion , head ache, or weakness not preceeded aura. 1 episode in a month- 3 yrs. Started on CBZ and Levitiracetam, frequency of seizures increased to once in 10 days- 2 yrs.
  • 3. For the past one month 2-3 times a day, starts as a starring look followed by turning of head towards left side with deviation of eye towards left side,with tonic posturing of left hand followed by right hand, some times with clonic movements, with loss of consciousness lasting for 1-2 mnts, without any post ictal confusion or weakness, with or without preceeding aura • no head ache /vomiting/behavioural disturbances/limb weakness/cranial nerve disturbances/trauma
  • 4. • Past history: evaluated for epilepsy in 2004 ct plain was reported as calcified glioma, started on AED, 2008 AED dose increased and ct was repeated and was reported as calcified granuloma Antenatal natal post natal history, family history nil relevant
  • 5. • O/E : pt conscious, oriented thin bult, no neurocutaneous marker HMF: normal Lobar functions: normal Cranial nerves: normal Sms : normal Cerebellar function: normal Spine and cranium: normal
  • 7. MRI 3.5*2.5*2.5*cm sized T1 &T2 hetero intense lesion noted in the right superior middle temporal gyrus with cortical expansion. Calvarial remodelling noted in the adjacent right temporal lobe. No evidence of diffusion restriction in the cortical lesion, minimal heterogenous enhancement noted in the lesion. Evidence of blooming in GRE D/D DNET Oligidendroglioma Ganglioglioma
  • 8.
  • 9.
  • 10. • EEG- normal study • Other investigations- normal
  • 12. Surgery • Right temporal craniotomy, trans cortical approach and total excision of tumor done, the tumor was soft, with areas of old hemorrhages and calcification.
  • 13. Biopsy • Squash : tuberculoma • HPE– suggestive of vascular tumor - angioma
  • 14. Post opertative • No fits after surgery • On AED – dose is being taperd
  • 16. Post op EEG • Background shows well formed alpha waves in posterior head regions, responding normally to eye opening. Bilateral sharp waves and spikes seen more during hyperventilation and after hyperventilation. No slow waves seen. • Imp : abnormal record suggestive of bilateral epileptiform avtivity
  • 17. What is lesional epilepsy? • In some patients with longstanding epilepsy the cause of the seizure may be a slow growing tumors , vascular malformations, infections or congenital anomalies. These lesions are picked up in the MRI. • Removal of the lesion may cure a patients with epilepsy
  • 18. Classification • Temporal lobe epilepsy • Extra temporal lobe lesional epilepsy • Subcortical lesional epilepsy • Catastrophic epilepsy
  • 19. Temporal lobe and extra temporal lobe lesional epilepsy • Neoplastic- eg. Astrocytoma, ganglioglioma,pleomorphic xanthoastrocytoma, DNET • Vascular-eg. Cavernous hemangioma, arteriovenous malformation, angioma • Dysgenetic -eg. Focal or diffuse cortical dysplasia, sturge weber syndrome, tuberous sclerosis • Traumatic • Ischemic
  • 20. Subcortical epilepsy • Hypothalamic hamartoma • Cerebellar seizures
  • 21. Catastrophic epilepsy • Hemimegalencephaly • Diffuse cortical dysplasias • Rasmussens • Porencephalic cyst
  • 22. Long term seizure control after lesionectomy 9 years follow up of 53 patients operated for supra tentorial cavernomas: 45 (84.9%)pts- free from disabling seizure- Engels class1 37(69.8%)pts –completely free of post op seizure Engels class 1A International league against epilesy JNS nov 2008- volume 63
  • 23. • 22 out of 26 cases -84.6% of seizure control after surgery for temporal lobe ganglioglima (Morris et al) • Complete seizure relief in12 of16 patients(75%) operated for DNET Raymond et al
  • 24. Predictors of seizure control after surgery • Lower pre op frequency of partial seizure associated with better outcome • Presence of CPS – supportive predictive parameters for satisfactory seizure relief • Secondary seizure generalization- negative predictor for seizure control • Because of very low rate of patients with discordant EEG patterns , information derived from EEG recordings is not suitable to discriminate patients with a lower expectation of seizure control. • Other studies found a significant contribution of EEG data in predicting outcome after surgery especially in patients with mesial temporal sclerosis.