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Table of Content - Volume 21 Issue 2 - February 2022


 

Study of role of MRI in evaluation of pediatric epilepsy at a tertiary hospital

 

Ankita S Mundhe1*, Balaji H Kombade2

                   

1Resident (JR3), 2Associate Professor, Department of Radiodiagnosis, Vilasrao Deshmukh Government Medical College, Latur, Maharashtra.

Email: ankitamundhe009@gmail.com, bhkombde@yahoo.com

Abstract              Background: Epilepsy is a disease characterized by spontaneous recurrence of unprovoked seizures. Many focal lesions/ pathologies responsible for epilepsy are identified with neuroimaging. The imaging modality of choice is MRI because of its superior resolution compared to CT and USG. Material And Methods: Present study was Hospital based prospective study, conducted in pediatric patients (age under 12 years) referred from OPD and IPD who presented with epilepsy, underwent MRI study. Results: Out of 100 patients, most common age group in our study was 10-12yrs age (33%) followed by 0-3 yrs (29 %). 58 patients (58%) were males and 42 patients (42%) were females. Male: Female ratio 1.3:1. 60patients(60%)presented with Generalized seizures, 29 patients (29%) presented with focal seizures while 11 patients (11%) had an unknown onset. Out of 100 patients studied, 85 patients (85%) had positive findings on MRI while 15 patients (15%) had normal MRI with no detectable lesions. In the study, the most common cause of epilepsy was infection (35%), followed by anoxia and hypoxic ischemic encephalopathy (HIE) (17%), malformations of cortical development (MCD) (8.2%), acquired metabolic disorders and vascular causes (3.5%) each. The most common etiology seen on MRI was infection in all age groups except 0-3yrs age group where anoxia and HIE was most common etiology while infection was second most common etiology. Conclusion: MRI plays a significant role in evaluation of pediatric patients presenting with epilepsy and it is the first imaging modality of choice with proper MRI seizure protocol to establish the correct diagnosis, plan the management according to diagnosis as well as helps in prognosis.

Keywords: MRI, pediatric epilepsy, refractory seizures, infectious etiology

 

INTRODUCTION

Epilepsy is a disease characterized by spontaneous recurrence of unprovoked seizures. Seizures are time-limited paroxysmal events that result from abnormal, involuntary, rhythmic neuronal discharges in the brain.1 Epilepsy is one of the most common neurologic conditions, with an incidence of approximately 50 new cases per year per 100,000 population.2 Diagnosis of seizure involves identifying the symptoms, clinical diagnosis of the case, laboratory evaluation, EEG recording, lumbar puncture in suspected meningitis and neuroimaging.3,4 Recent advances in neuroimaging play an important role in the diagnosis, management and in guiding the treatment of pediatric epilepsy. Functional neuroimaging provides further information and may show abnormalities even in cases where MRI was normal, thus further helping in the localization of the epileptogenic foci and guiding the possible surgical management of intractable/refractory epilepsy when indicated.5 Many focal lesions/ pathologies responsible for epilepsy are identified with neuroimaging. The yield of neuroimaging is high even in low risk groups.6 The imaging modality of choice is MRI because of its superior resolution compared to CT and USG.7 MRI provides detailed evaluation of small lesion, radiation free. Present study was aimed to study of role of MRI in evaluation of paediatric epilepsy at a tertiary hospital.

              

MATERIAL AND METHODS

Present study was Hospital based prospective study, conducted in Department of Radiodiagnosis, Vilasrao Deshmukh Government Medical College, Latur, India. Study duration was of 2 years (July 2018 to June 2019). Study was approved by institutional ethical committee.

Inclusion criteria: All pediatric patients (age under 12 years) referred from OPD and IPD who presented with epilepsy

Exclusion criteria: Claustrophobicpatients, Patients with metallic implants considered contraindicated for MRIimaging. Patients with trauma. Patients with febrile seizuredisorders.

First informed consent was taken from parents/accompanying relatives after giving proper information of the MRIscan. Then patient was screened for ferromagnetic objects and aneurysm clipsetc.

Complete clinical history, birth and vaccination history, family history and past history of patient was noted. The points noted were type of seizure, duration of illness and any associatedcomplaints. Physical examination findings as for evidence of any neurocutaneous stigmata and complete CNS examination findings were noted. Biochemical investigations like complete blood profile, liver and renal function tests, blood glucose levels, blood electrolytes levels as advised by physician were noted. Other laboratory parameters like Biochemical levels forleukodystrophies, Serological studies forinfections and CSF examination.

Findings of EEG and CT scan if done were documented. Very few cases had EEG documentation which was correlated with imaging findings. For MRI, patient was positioned supine on scanning table, immobilization of the patient’s head was achieved and the head coil was applied. Patients were subjected to MRI scanning. When necessary, adequate sedation was given by the anaesthetist. Magnetic Resonance Imaging was done with Machine, 1.5 Tesla GE SIGNA MRISYSTEM, Radiofrequency coil—Sense headcoil, excellent resolution, field of view was kept as small as possible (approximately 20 cms), Slice thickness-- usually 3-5 mm, Interslicegap 1mm and Matrix 256 x256. Conventional MR imaging was performed by taking T1W (TE 8.0 ms, TR 480 ms), T2W (TE 102.9 ms, TR 4780 ms), and FLAIR (TE 92.2 ms, TR 8002 ms) sequences in planes as mentioned below. Post gadolinium (dose 0.1mmol/kg) enhanced MRI was performed in Axial and Sagittal planes in selected cases depending on findings on non- contrast study or clinical suspicion. DWI (TE 83 ms, TR 5025 ms) and GRE (Gradient recalled echo) axial performed in all cases. When required, MR spectroscopy, Venous 3D PCA (Phase Contrast Angiography) and MR angiography including TOF was done.

Pulse sequences and imaging planes: T1 Sagittal and Axial Pre and Post contrast. T2 Axial and Coronal. FLAIR Axial. DWI (Diffusion Weighted Imaging) Axial GRE (Gradient Recalled Echo) Axial. T1 Inversion Recovery sequence.

In suspected temporal lobe epilepsy additional sequences are: T1 angled coronal, T1 3D isotropic acquisition. FLAIR angled coronal, T2 angled coronal, MR Spectroscopy, Venous 3D PCA (Phase Contrast Angiography) and MR angiography including TOF if required.

MRI scans were studied with respect to: Number of lesions present., Unilateral or Bilateral, Site, Signalintensity, Any hemorrhage, Calcifications. Surrounding edema, Mass effect, Diffusion restriction, Contrast enhancement/enhancing lesion. Abnormal meningeal enhancement, Atrophy, Hydrocephalus, MR spectroscopy findings. Any other significant positive finding Final diagnosis was based on the medical history, clinical presentation, EEG and CT correlation, followup CSF analysis, pathological, surgical findings when available and\ response to medical therapy. In inconclusive cases it was made by follow up MRI and treatment response. MRI Brain findings were noted and recorded. The management decision, follow up and outcome recorded. Statistical analysis–Data was collected and entered in MS Excel.

 

RESULTS

This study includes MRI brain evaluation of 100 cases of pediatric patients aged 0- 12 years. Most common age group in our study was 10-12yrs age (33%) followed by 0-3 yrs (29 %). 58 patients (58%) were males and 42 patients (42%) were females. Male: Female ratio 1.3:1.

Table 1: Age And gender Distribution

Age Group (In Years)

Male

Female

Total

0-3

16

13

29

4-6

14

4

18

7-9

11

9

20

10-12

17

16

33

TOTAL

58

42

100

60patients(60%)presented with Generalized seizures, 29 patients (29%) presented with focal seizures while 11 patients (11%) had an unknown onset.

Table 2: Distribution according to types of seizure

Types of Seizure

No. of patients

Percentage (%)

Generalized

60

60

Focal

29

29

Unknown

11

11

TOTAL

100

100

 

In table 3, Out of 100 patients studied, 85 patients (85%) had positive findings on MRI while 15 patients (15%) had normal MRI with no detectable lesions. In the study, the most common cause of epilepsy was infection (35%), followed by anoxia and hypoxic ischemic encephalopathy (HIE) (17%), malformations of cortical development (MCD) (8.2%), acquired metabolic disorders and vascular causes (3.5%) each. In our study, total 32 patients reported to have infection, tuberculosis (40.6%), encephalitis (9.3%), meningitis (21.8%), meninigo-encephalitis (9.3%), viral infection (12.5%) were common findings. It was noted that Mesial Temporal sclerosis was most common cause of isolated temporal lobe epilepsy. Hippocampal atrophy and secondary changes were found in 100% while Hippocampal T2 and FLAIR Hyper intensity and abnormal architecture were seen in 75% patients. 7 patients had malformations of cortical development. Focal cortical is dyplasia was seen in 2 patients (14.2%) while rest of the pathologies like microcephaly, agyria, lissencephaly, polymicrogyria, heterotopia, schizencephaly were seen in one patient each (7.1%) cortical developmental malformations presented with epilepsy in early age group, particularly in infancy (<1 year of age). Out of 3 patients with acquired toxic- metabolic disorders, 1 patient each had Chronic bilirubin encephalopathy, PRES (posterior reversible encephalopathy syndrome) secondary to hypertension and Medication-Related Leukoencephalopathy. Outof5patientsof neoplasticetiology, 1 patient each had DNET, ganglio-glioma, glioma, pilocystic astrocytoma and glioblastoma multiforme. Vascular pathology was noted in 3patients. 2 patients (66.6%) has arterial infarct and one had Vasculitis. Out of 2 patients presenting with demyelination on MRI, one patient had ADEM while other patient had tumefactive demyelination.


 

Table 3: Etiology on MRI

MRI findings

No. of patients

Percentage(%)

MRI IMAGING

 

 

Normal

15

15 %

Abnormal

85

85 %

Type of Etiology

 

 

Infection

32

37

Tuberculosis

13

40.6%

Meningitis(excluding tuberculous)

7

21.8%

Viral (Meningitis, encephalitis)

4

12.5%

Encephalitis

3

9.3%

Meningoencephalitis (excluding tuberculous)

3

9.3%

Rasmussen's encephalitis

1

3.12%

Hydatid cyst

1

3.12%

Anoxia and Hypoxic Ischemic Encephalopathy

15

17

Miscellaneous

12

14

Post ictal edema

7

58.3

Hydrocephalus

3

25.0

Arachnoid cyst

1

8.3

Subdural Hygroma

1

8.3

Malformations of Cortical Development

7

8.2

Microcephalywithagyria

1

7.1

Lissencephaly

1

7.1

Polymicrogyria

1

7.1

Focalcorticaldysplasia

2

14.2

Heterotopia

1

7.1

Schizencephaly

1

7.1

Neoplasm

5

5.8

DNET

1

20

Ganglioglioma

1

20

Glioma

1

20

Pilocytic astrocytoma

1

20

Glioblastoma multiforme

1

20

Mesial Temporal Sclerosis

4

4.7

Hippocampal atrophy

4(100%)

 

Hippocampal T2 and FLAIR Hyper intensity

3(75%)

 

Loss of hippocampal architecture

3(75%)

 

Secondary changes (Temporal horn dilatation, caudate nucleus atrophy and hypointensity in T1W images)

4(100%)

 

Vascular

3

3.5

Arterial infarct (excluding tuberculous)

2

66.6

Vasculitis

1

33.3

Acquired metabolic disorders

3

3.5

Chronic bilirubin encephalopathy

1

33.33

PRES (posterior reversible encephalopathysyndrome)

1

33.33

Medication-Related Leukoencephalopathy

1

33.33

Demyelinating Diseases

2

2.3

ADEM

1

50

Tumefactive demylination

1

50

Phakomatoses (Tuberous sclerosis)

1

1.1

Inherited metabolic disorders (Metachromatic Leukodystrophy)

1

1.1

 

In our study, isolated temporal lobe lesion was cause of epilepsy in 6 patients. Out of 6 patients Mesial Temporal sclerosis was found in 4 patients (66.6%), Glioma and ganglioglioma was found 1 patient (16.6%) each.

Table 4: Isolated temporal lobe epilepsy (N= 6 )

Pathologies

No. of patients

Percentage (%)

Mesial Temporal sclerosis

4

66.6

Glioma

1

16.6

Ganglioglioma

1

16.6

 

In our study out of 100 patients, 85 patients showed abnormal finding on MRI. In our study the most common age group showing pathology on MRI was 10-12yrs age, followed by 0-3yrs age group.The most common etiology seen on MRI was infection in all age groups except 0-3yrs age group where anoxia and HIE was most common etiology while infection was second most common etiology. In age group 0-3yrs, there were total 27 patients (31.7%) with positive MRI, common etiologies were anoxia and HIE (8 patients), followed by infection (7 patients), and malformations of cortical development (3 patients). In age group 4-6yrs, total 14 (16.4%) had pathologies on MRI, infection was found to be most common cause (6 patients), followed by acquired metabolic diseases and miscellaneous (2 patients each). In age group 7-9yrs, total 14 (17.6%) had pathologies on MRI, infection was reported as most common cause (7 patients), followed by anoxia HIE and neoplasm (2 patients each). In age group 10-12yrs, total 29 (34.1%) had pathologies on MRI, infection was seen as most common etiology (12 patients), followed by anoxia and HIE (4 patients).

Table 5: Distribution of various types of etiologies according to age group (n=85)

Type of Etiology

0-3

Yrs

4-6

Yrs

7-9

Yrs.

10-

12 Yrs.

TOTAL

Mesial Temporal Sclerosis

2

1

1

0

4

Malformations of CorticalDevelopment

3

1

1

2

7

Phakomatoses

0

0

0

1

1

Inherited metabolic disorders

1

0

0

0

1

Acquired metabolic disorders

0

2

1

0

3

Anoxia and Hypoxic Ischemic Encephalopathy

8

1

2

4

15

Infection

7

6

7

12

32

Demyelinating Diseases

0

0

0

2

2

Neoplasm

0

1

2

2

5

Vascular

1

0

0

2

3

Miscellaneous

5

2

1

4

12

TOTAL

27

14

15

29

85

 

                         Figure 1: AXIAL FLAIR                       Figure 2: COR T2                      Figure 3: AXIAL T1                                                                                 Figure 4: AXIAL T1 FAT SAT

                                                                                                                                                                            POST CONTRAST

A well-defined T1 isointense and T2 hypointense lesion showing peripheral ring like enhancement without diffusion restriction with moderate adjacent vasogenic edema seen in left parietal lobe

               Figure 5: AXIAL FLAIR                  Figure 6: T1 FAT SATPRECONTRAST     Figure 7: T1 FAT SATPOSTCONTRAST

FLAIR hyperintentense lesion in left temporal lobe with minimal adjacent edema without post contrast enhancement

 

Figure 8: AXIAL FLAIR AXIAL FLAIR

Cystic changes in bilateral subcortical white matter with adjacent gliosis and atrophy

 


DISCUSSION

In present study, out of 100 patients maximum number of patients in the study were in the age group of 10-12 years (33%) followed by 0-3 years (29%). The mean age in our study was 6.2yrs. Similar findings were noted by Gulati P et al.,8 in which maximum patients were in the age group 6-12 years. However the mean age our study is slightly lesser than the study by Wongladarom S et al.,9(mean age was 7 years and 5 months). In our study of 100patients, 58% were males and 42% were females. Male : Female ratio was1.2:1. Our study correlates with the study done by Sanghvi JP et al.,10in which 60.5% were males and 31.7% werefemales. It also correlates with the study done by Amirsalari S et al.,11in which there were 57.7% boys and 42.5% girls. In our study of 95 patients, maximum number of patients, 60% presented with Generalized seizures, 29% had focal seizure and 11 % were unknown type at presentation. Our study has similar results as that of study done by Rasool A et al.,12in which 276 patients were studied. In this study it was found that generalized seizures constituted the major seizure group (42%), followed by partial seizures (31.2%) and complex febrile seizure (23.2%). Our study also correlates with the study done by Chaurasia R et al.,13in which generalized seizures accounted for the major number of patients seen in 76.7%. In this study of total 100 patients, 85 patients (85%) had abnormal MRI findings. Our study is comparable with the study done by Kuzniecky R et al.,14in which MRI revealed abnormalities in 84% of patients. Resta et al.,14 reported positive MRI in 51.3%, Wang et al.,15in 41.7% and Chang et al.,16in 48.9%. Our study shows a higher percentage, probably because of strict exclusion criteria’s, which shows that patient selection, plays an important role in MR positivity rates. In our study, In the study, the most common cause of epilepsy was infection (35%), followed by anoxia and hypoxic ischemic encephalopathy (HIE) (17%), miscellaneous causes (14%) and malformations of cortical development (MCD) (8.2%). Similar findings were noted by Aarti Aanandet al.,18where 95 children under the age of 12 years were studied, infection (29.8%) was the most common etiology followed by anoxia and hypoxic-ischemic encephalopathy. Ojaswi B khandediya et al.,19 also noted that infection was the most common etiology followed by Mesial temporal sclerosis and focal cortical dysplasia. In present study, isolated temporal lobe lesion was cause of epilepsy in 6 patients, and Mesial Temporal sclerosis (4 patients) and Glioma and ganglioglioma (1 patient each) were common causes. Our study correlates with study done by J D Grattan Smith et al.,20in which mesial temporal sclerosis was most common cause of temporal lobe epilepsy seen in 30 out of 53 children (57%), followed by tumours in 8 (15%), cavernous angioma in 1(1.8%) and ectopic gray matter in 1(1.8%) ofpatients. Sales LV et al.,21 in which out of 31 patients with temporal lobe epilepsy, most common pathology was mesial temporal sclerosis seen in 9 (29.0%), dysplasia in 8 (25.8%), tumors in 2(6.4%), arachnoid cyst in 1 (3.2%) and choroid cyst in 1 (3.2%). In present study, 32 patients reported to had infection, tuberculosis (40.6%), encephalitis (9.3%), meningitis (21.8%), meninigo-encephalitis (9.3%), viral infection (12.5%) were common findings. Out of 13 patient of tuberculosis, 8 patients (61.5%) had leptomeningeal enhancement, 3 patients (23.07%) had tuberculoma, and 1 patient (7.6%) each of hydrocephalus and encephalitis. In Gulati P, Jena A.N. et al.,8study, out of 345 patients with abnormal MRI, tuberculoma was the most common etiology and was seen in 98 (28.4%), followed by neurocysticercosis in 86(24.9%). In Chaurasia R et al.,22 study, most common cause of epilepsy was CNS tuberculosis (30.3%), followed by Neurocysticercosis (11.0%) and Encephalitis (7.9%). However, our study is in discordance with Parihar Ravi Kumar et al.,23 study, in which most common etiology was neurocysticercosis (55.81%) followed by tuberculoma (29.91%). In study by Mittal GK et al.,24 out of 54 patients with Malformations of cortical development, Focal cortical dysplasia was the most common pathology reported in 16 patients (29.6%), next was Schizencephalyin8(14.8%),Polymicrogyriain8(14.8%),DNETin6(11.1%).Similar findings were noted in present study. For etiology in age group 0-3 years, our study correlates well with Khreisat WH et al.,25study, most common etiological factor found in this study was perinatal asphyxia seen in 55%, followed by CNS infection in 15%, anomalies of central nervous system in (9%), head injuries in (8%), congenital and prematurity in(5%).

For etiology in older age group, our study correlates with Parihar Ravi Kumar et al.,23study, in which children in the age group of 28days to 18 years with partial seizures were studied. 6 patients (66.6%) in age group of 28days-5years, 18 patients (85.7%) in age group of >5-10years and 12 patients (92.3%) in age group >10-18years had infection as the most common etiology. Thus infection had major burden in causing epilepsy with increasing age group. For etiology in older age group, our study also correlates with Gulati P et al.,8study, in which 170 children with chronic seizures were studied. Age distribution was done as follows: 0-1 year, 1-3 year, 3-6 year and 6-12 year. The etiologies were classified into Infections (tuberculomas, neurocysticercosis, meningitis), atrophy, vascular and miscellaneous causes. Infection was most common etiology in 6-12 years age group seen in 51.1%, followed by miscellaneous in 16.4%. In age group 0-1, 1-3 and 3-6 years, infection was seen in 4.7%, 4.1% and 3 %respectively. MRI plays an invaluable role in the evaluation of pediatric patients with seizure disorder. Accurate diagnosis of cause of seizure is important for treatment decision. With its high spatial resolution, excellent inherent soft tissue contrast, multi-planar imaging capability and lack of ionizing radiation; MRI has emerged as a versatile tool in imaging of pediatric patients with seizures. MRI not only identifies specific epileptogenic substrates, but also helps in determining specific treatment and predicts prognosis. Employing appropriate imaging protocols and reviewing the images in systemic manner helps in the identification of subtle epileptogenic structural abnormalities. MR imaging is superior neuroimaging with no radiation exposure and could be the first investigation of choice in epileptic syndrome, developmental cortical malformations, mesial temporal sclerosis. Its ability in identifying subtle lesions, location and extent of the lesions is excellent.

 

CONCLUSION

MRI plays a significant role in evaluation of pediatric patients presenting with epilepsy and it is the first imaging modality of choice with proper MRI seizure protocol to establish the correct diagnosis, plan the management according to diagnosis as well as helps in prognosis. MRI helps in evaluation of patients presenting with refractory seizures undiagnosed by other imaging modalities and children with newly diagnosed epilepsy especially those with abnormal neurological examination, focal seizures or focal EEG abnormalities.

 

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