Gloria J. Guzmán, MD, MSc Robert McKinstry, MD, PhD Matthew Smyth, MD, FAANS, FACS, FAAP.

Slides:



Advertisements
Similar presentations
E Feoli MD North East Regional Epilepsy Group 2012
Advertisements

1 Muscle artifact removal in an Epilepsy Monitoring Unit Highlighted application:
A CASE REPORT OF HEMIMEGALENCEPHALY K MRAIDHA, S JERBI OMEZZINE, N CHOUCHENE, Z KHADIMALLAH, A ACHOUR, R BOSSOFFARA 1, MT Sfar 1, HA HAMZA. Department.
© 2014 Direct One Communications, Inc. All rights reserved. 1 New Insights into the Basic Mechanisms, Diagnosis, and Staging of Epilepsy Nicole Odom, MD.
Neuroimaging of Epilepsy
Video-EEG Monitoring in Childhood Epilepsy
Dementia with Lewy Bodies
Responsive Neuro-Stimulation
Giving Me Fits: Improved Detection of Subtle Abnormalities in Epilepsy Elliott Friedman and Maria Olga Patino eEdE-07.
M. AMOR, S. MAJDOUB, B. BEN SALAH, M. DHIFALLAH, H. ZAGHOUANI, T. RZIGA, H. AMARA, D. BAKIR, C. KRAIEM Radiology service, University Hospital Farhat Hached.
Gloria J. Guzman, MD, MSc Christopher Owen, MA Dan Marcus, PhD Russ Hornbeck, MCSC Matthew Smyth, MD, FAANS, FACS, FAAP Tammie Lee Benzinger, MD, PhD.
The Role of Imaging in Sinusitis Dr Mohamed El Safwany, MD.
Cortical dysplasia 소아과 R3 황대환.
A ACHOUR, S JERBI OMEZZINE, S YOUNES 1, S BOUABID, MH SFAR 1, HA HAMZA. Department of Medical Imaging, Tahar Sfar University Hospital Center, Mahdia, Tunisia.
Case Study 58 Kenneth Clark, MD. Question 1 This is a 4-year-old boy with refractory epilepsy attributable to the right temporal region. An MRI as well.
Jalal Jalal Shokouhi – MD Editor in Chief of Iranian Society of Radiology
Idoia Corcuera-Solano, Gerard Reddy, Bradley Delman, Reade De Leacy, Dan Rettmann, Lawrence N Tanenbaum EP
Transmantle sign and focal cortical dysplasia
Case Study 50 Edward D. Plowey. Case History The patient is a 2 year old girl with normal birth and developmental histories who presented with new onset.
Differentiation of Peri-Ictal Pseudoprogression from Tumor Recurrence in a Patient with Treated Glioma: Value of Diffusion Weighted and Perfusion Imaging.
Definition of epilepsy
Task 3: Brain Abnormality Research involving MRI and CAT scan research on live patients has found the following structural abnormalities in the schizophrenic.
Abstract Cerebral cavernous malformations (CCM) are lesions found in the brain and spinal cord comprised of abnormal blood cells, which bleed sporadically.
Responsive Neurostimulation (RNS) for the treatment of epilepsy
AANP: Diagnostic Slide Session – Case 04 Tracie Pham, M.D., William H. Yong, M.D., Gary W. Mathern, M.D., and Harry V. Vinters, M.D. UCLA Department of.
1960s, 1970s, converging evidence from cognitive neuropsychology, psychology, neurobiology support the view of Multiple memory systems, efforts to experimentally.
American Epilepsy Society
NYU Medical Grand Rounds Clinical Vignette Megha Shah PGY-2 November 10, 2010 U NITED S TATES D EPARTMENT OF V ETERANS A FFAIRS.
Case Study 10 Harry Kellermier, M.D.. The patient is a 27-year-old female with a history of complex partial seizures starting at age 16. A typical episode.
COMPARATIVE LATERALIZING ABILITY of MULTIMODALITY MR IMAGING in TEMPORAL LOBE EPILEPSY ¹ Karabekir Ercan, M.D. ¹ ¹ H.Pinar Gunbey, M.D. ¹ ¹ Elcin Zan,
T2 FLAIR Increased Signal Intensity at the Posterior Limb of the Internal Capsule: Clinical Significance in ALS Patients G. Protogerou 1, S. Ralli 2, I.
Núria Bargalló, Teresa Lema,Mar Carreño, Antonio Donaire, Javier Aparicio, Iratxe Maestro. Hospital Clínic i Provincial de Barcelona MRI Changes In Status.
Background Information Epilepsy is a neurological disorder that characterized by recurrent seizures. It is estimated to affect over 70 million people.
Sint Lucas-Andreas Hospital, Amsterdam
Tuberous Sclerosis Abdullah M. Al-Olayan MBBS, SBP, ABP
Date of download: 6/23/2016 Copyright © 2016 McGraw-Hill Education. All rights reserved. Supplementary Sensorimotor Area (SSMA) Seizure; Subdural vs Scalp.
S. CONDETTE-AULIAC 1, A. BOULIN 1, O. COSKUN 1, L. BOZEC-LE MOAL 2, S. ALDEA 3, S.GUIEU 1, G. RODESCH 1. 1 Neuroradiology department, 2 Oncology department,
Imaging of Epilepsy Ali Jassim Alhashli Year IV – Unit VIII (CNS) – Problem 6.
Reversible posterior leukoencephalopathy syndrome and silent cerebral infarcts are associated with severe acute chest syndrome in children with sickle.
The NeuroPace RNS® System and Surgical Options
Fig. 5. Both imaging and lesion factors in case 3 with focal cortical dysplasia. A. Axial T2-weighted initial MR image (1.5T, non-epilepsy protocol) obtained.
Focal cortical dysplasia (FCD) is often associated with severe focal epilepsy. Intraoperative ECoG showed one of the following patterns: (1) repetitive.
Angela Lignelli, MD, Alexander G. Khandji, MD  Neurosurgery Clinics 
Epilepsy, hippocampal sclerosis and amygdalar atrophy following H1N1-influenza- associated encephalopathy in an adult  Shirin Karimi, Taufik A. Valiante,
MRI Scanning in Epilepsy
Epilepsy in Diagnostic Imaging
Stereo-EEG, radiofrequency thermocoagulation and neuropathological correlations in a patient with MRI-negative type IIb focal cortical dysplasia  Rita.
Nat. Rev. Neurol. doi: /nrneurol
Epilepsy: Contemporary Perspectives on Evaluation and Treatment
Neuro-oncology Board Review
How I treat and manage strokes in sickle cell disease
Reversible posterior leukoencephalopathy syndrome and silent cerebral infarcts are associated with severe acute chest syndrome in children with sickle.
Correlation of MRI and histopathology in epileptogenic parietal and occipital lobe lesions  Horst Urbach, Devin Binder, Marec von Lehe, Martin Podlogar,
MR images of cytoarchitectural dysplasia
Stephen L. Hauser, Jorge R. Oksenberg  Neuron 
L.D MEWASINGH, F CHRISTIAENS, A AEBY, C CHRISTOPHE, B DAN 
Genetic Malformations of the Human Cerebral Cortex
Seizures caused by brain tumors in children
Rasmussen's encephalitis: Experience from a developing country based on a group of medically and surgically treated patients  K.N. Ramesha, B. Rajesh,
Susceptibility-Weighted Imaging and Proton Magnetic Resonance Spectroscopy in Assessment of Outcome After Pediatric Traumatic Brain Injury  Stephen Ashwal,
Neuropathology of epilepsy: epilepsy-related deaths and SUDEP
IMAGING MODALITIES Computerized Tomography Magnetic Resonance Imaging.
Radiological findings of Posterior Reversible Encephalopathy Syndrome in transplanted children previous affected by hemoglobinopathy: A neuroimaging retrospective.
MR images of Taylor’s FCD with balloon cells
Hashimoto encephalitis.
MR images of Taylor’s FCD without balloon cells
Figure 3 Changing appearance of the frontal cortex with age associated with increasing myelination Changing appearance of the frontal cortex with age associated.
Images of a 22-month-old male patient with severe left temporal lobe epilepsy that was recognized at age 9 months after bacterial meningitis at age 6 months.A.
MR scans of brain and spine: (A) sagittal T2 image showing signal change in the posterior spinal cord between C3 and T6. MR scans of brain and spine: (A)
Curvilinear reformations show relative position of subdural electrode contacts to a cortical dysplasia located deep in the left frontal lobe. Curvilinear.
Presentation transcript:

Gloria J. Guzmán, MD, MSc Robert McKinstry, MD, PhD Matthew Smyth, MD, FAANS, FACS, FAAP

Financial Disclosures Gloria Guzman and Matthew Smyth: None Robert McKinstry: Siemens Healthcare: Honoraria, travel, lodging, meals >$10,000

PURPOSE

To create an imaging primer that will allow easier radiographic identification of focal cortical dysplasias

APPROACH/METHODS

What is focal cortical dysplasia (FCD)? 1, 2 Focal cortical dysplasia is a derangement of cortical development, including neuronal proliferation, migration, differentiation or programmed cell death Both genetic and acquired factors are involved, although the pathogenesis is still being investigated Multiple grading systems exist. In general, three types are recognized (I, II and III), each with associated sub- classifications. We will focus on FCD type I and II, which are isolated lesions. FCD type III are associated with other findings, such as tumor, vascular malformations or sclerosis 1.Colombo et at. Imaging of malformations of cortical development. Epileptic Disord 2009; 11 (3): Blümcke et al. The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission. Epilepsia, 52(1):158–174, 2011

Imaging findings of FCD Type I 1, 2 Temporal predilection, more common in adults Prominent lobar/sublobar hypoplasia/atrophy, frequently associated with volume loss of the subcortical white matter: Moderately increased signal on T2WI and heavily T2W FLAIR images Decreased signal on T1W images, either 3D volumetric Gradient Echo T1W or heavily T1W Inversion Recovery (IR) images Mild blurring at the grey/white matter junction with normal cortical thickness Abnormal gyral/sulcal patterns can be present Most commonly associated with dual pathology (+ hippocampal sclerosis) 1, which will not be discussed in this presentation, as it is “not yet comprehensively defined” 2 1.Colombo et at. Imaging of malformations of cortical development. Epileptic Disord 2009; 11 (3): Blümcke et al. The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission. Epilepsia, 52(1):158–174, 2011

Imaging findings of FCD Type II 1,2 Extratemporal with predilection of frontal lobes, more common in children Transmantle sign: The white matter signal alterations taper towards the ventricle, reflecting the involvement of radial glial- neuronal bands Increased cortical thickness Pronounced blurring of the gray matter/white matter junction both on T1WI and T2WI (due to increase disturbance in cortical structures vs. FCD I) Increased subcortical white matter signal on T2WI and heavily T2W FLAIR Increased T2-signal within affected cortex is far more common in FCD type II than in FCD type I; the grey matter remains hypointense 1.Colombo et at. Imaging of malformations of cortical development. Epileptic Disord 2009; 11 (3): Blümcke et al. The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission. Epilepsia, 52(1):158–174, 2011

Imaging findings of FCD Type II 1,2 Decreased signal on T1W images, either 3D volumetric Gradient Echo T1W or heavily T1W Inversion Recovery (IR) images Abnormal cortical gyration and sulcation, better evaluated on 3D surface rendering Focal enlargement of the subarachnoid spaces seem to point at the dysplastic lesion In a number of cases, a much sharper demarcation between the cortex and the adjacent white matter may be found 1.Colombo et at. Imaging of malformations of cortical development. Epileptic Disord 2009; 11 (3): Blümcke et al. The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission. Epilepsia, 52(1):158–174, 2011

Detailed analysis of following structures by imaging: Increased cortical thickness Blurring of the grey/white matter junction with disappearance of subcortical white matter digitations White matter signal abnormalities with or without extension all throughout the cortical mantle (the transmantle sign) Focal enlargement of subarachnoid space adjacent to cortical anomaly Grey and/or white matter signal changes Abnormal gyral/sulcal patterns Focal and/or lobar hypoplasia/atrophy The Checklist

Detailed analysis of the following structures: Increased cortical thickness

Detailed analysis of the following structures: Blurring of the grey/white matter junction with disappearance of subcortical white matter digitations

Detailed analysis of the following structures: White matter signal abnormalities with or without extension all throughout the cortical mantle (the transmantle sign)

Detailed analysis of the following structures: Focal enlargement of the subarachnoid spaces

Grey and/or white matter signal changes Detailed analysis of the following structures:

Abnormal gyral/sulcal patterns

Detailed analysis of the following structures: Focal and/or lobar hypoplasia/atrophy

Caveats in analysis: Cortical thickening should only be reported if the cortex appears thick on both T1W and T2W sequences that are windowed for high levels of contrast, in at least two planes Blurring and cortical thickness should be evaluated specifically and individually on: T2WI 3D volumetric Gradient Echo T1WI Heavily T1W Inversion Recovery (IR) images

Analysis in infants 1 : In FCD, the subcortical white matter may sometimes be isointense to cortex (and, therefore, appear as blurring or thick cortex) on T1WI but will look hyperintense to cortex on T2WI, delineating the junction with the cortex and showing true cortical thickness, THUS YOUR T2 SEQUENCE IS THE MOST IMPORTANT Before 6 months of age, the hypointensity on T2W images of the cortical dysplasia is very clear in contrast to the hyperintensity of the unmyelinated white matter If the first MR study is obtained between ages of 6 and 18 months, a second scan will be required when myelination is largely completed (after the age of 30 months) 1.Colombo et at. Imaging of malformations of cortical development. Epileptic Disord 2009; 11 (3):

FINDINGS/DISCUSSION

CASES

Case #1 Where are the findings? Have you used your checklist? √ Cortical thickening √ Blurring of grey/white matter junction

17 y/o with intractable dominant motor cortical seizures No seizures since surgery 5/2008 Continues on Trileptal at 600 mg twice daily Case #1 Subtype of FCD not reported / not available

Case #2 Where are the findings? Have you used your checklist? √ Cortical thickening √ Blurring of grey/white matter junction

13 y/o with medically refractory epilepsy No seizures since surgery 7/2009 On Dilantin, last active 10/2010 Case #2

Case #3 Where are the findings? Have you used your checklist? √ Cortical thickening √ Blurring of grey/white matter junction √ Abnormal white matter signal

10 y/o with medically intractable seizures No seizures since surgery 10/2007 Weaned off Lamictal 2010 Case #3

Case #4 Where are the findings? Have you used your checklist? √ Cortical thickening √ Blurring of grey/white matter junction √ Prominent subarachnoid space

11 y/o with seizures refractory to medical treatment No seizures since surgery 6/2008 Off meds since 9/2009 Case #4

Case #5 Where are the findings? Have you used your checklist? √ Cortical thickening √ Blurring of grey/white matter junction

Case #5 2 y/o with intractable seizures, surgery on 7/2013 Since surgery has had a new type of seizure involving his arms going up and who body stiffening without eye deviation Repeat MRI showed residual FCD

Case #6 √ Blurring of grey/white matter junction Where are the findings? Have you used your checklist?

19 month old with intractable seizures, surgery on 3/2014 No seizures since surgery Weaning off Lamictal Case #6

Case #7 Where are the findings? Have you used your checklist? √ Cortical thickening √ Blurring of grey/white matter junction √ Abnormal grey and white matter signal

5y/o with medically intractable epilepsy Improved, but persistent seizures after surgery 10/08 On Keppra, Lamictal, Strattera and Valium Case #7

Case #8 Where are the findings? Have you used your checklist? √ Abnormal gyral pattern √ Blurring of grey/white matter junction √ Abnormal grey and white matter signal √ Prominent subarachnoid space

16 y/o, unfortunately, lost to follow-up, no clinical history post-op available Case #8 Subtype of FCD not reported / not available

Case #9 Where are the findings? Have you used your checklist? √ Blurring of grey/white matter junction

17 y/o with medically intractable epilepsy Worsening seizures since surgery on 12/12, considering NeuroPace treatment Case #9 Subtype of FCD not reported / not available

Case #10 Where are the findings? Have you used your checklist? √ Cortical thickening √ Blurring of grey/white matter junction √ Abnormal white matter signal

9 y/o with medically intractable seizures, surgery on 6/2011 Seizure-free and off Valproic Acid Case #10

Surgical outcomes Several articles have been published about patient outcomes after surgical removal of suspected epileptic foci, a few specifically relating to FCD Articles report approximately 70% success rate in achieving seizure-free status (Engle Epilepsy Outcome Scale I). Most failures are associated with incomplete resection of seizure foci, either due to technique or nearness to critical functional areas 3 3. Cohen-Gadol, AA, et al. "Long-term outcome after epilepsy surgery for focal cortical dysplasia." Journal of neurosurgery (2004):

SUMMARY

In summary Focal cortical dysplasias can be hard to identify on imaging, thus USE THE CHECKLIST to help guide you in the identification of these lesions Since surgical treatment is currently the same regardless of FCD type, correct imaging identification of isolated FCD on imaging is more important than histologic classification for surgical planning and decision-making Correlation with functional imaging, such as PET- Brain or SPECT-Brain is very useful in localizing these lesions

References Colombo N et al. Imaging of malformations of cortical development. Epileptic Disord 2009: 11(3): Blümcke et al. The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission 1. Epilepsia 2011: 52(1), Cohen-Gadol AA, et al. "Long-term outcome after epilepsy surgery for focal cortical dysplasia." Journal of Neurosurgery” (2004): 101.1, 55-65

Thank you for your attention!