Investig Magn Reson Imaging.  2017 Jun;21(2):82-90. 10.13104/imri.2017.21.2.82.

MR Findings of Seizure-Related Cerebral Cortical Lesions during Periictal Period

Affiliations
  • 1Department of Radiology, Gyeongsang National University School of Medicine, Jinju, Korea. choids@gnu.ac.kr

Abstract

PURPOSE
This study investigated the MRI, MR angiography (MRA) and MR perfusion findings of seizure-related cerebral cortical lesions during the periictal period.
MATERIALS AND METHODS
From a retrospective review of the institutional database between 2011 and 2014, a total of 21 patients were included in this study. Two radiologists assessed periictal MRI, including MRA and MR perfusion, in patients with seizure-related cortical lesions. The parameters examined include: location of cortical abnormality, multiplicity of the affected cortical region, cerebral vascular dilatation, perfusion abnormality and other parenchymal lesions.
RESULTS
All patients showed T2 hyperintense cerebral cortical lesions with accompanying diffusion restriction, either unilateral (18/21, 85.7%) or bilateral (3/21, 14.3%). Of the 21 patients enrolled, 10 (47.6%) had concurrent T2 hyperintense thalamic lesions, and 10 (47.6%) showed hippocampal involvement. Of the 17 patients (81%) who underwent MRA, 13 (76.5%) showed vascular dilatation with increased flow signal in the cerebral arteries of the affected cortical regions. On MR perfusion, all 5 patients showed cortical hyperperfusion, corresponding to the region of cortical abnormalities.
CONCLUSION
Seizure-related cerebral cortical lesions are characterized by T2 and diffusion hyperintensities, with corresponding cerebral hyperperfusion and vascular dilatation. These findings can be helpful for making an accurate diagnosis in patients with seizure.

Keyword

Seizure; Cortical hyperintensity; Periictal period; Magnetic resonance imaging; Magnetic resonance angiography; Magnetic resonance perfusion

MeSH Terms

Angiography
Cerebral Arteries
Diagnosis
Diffusion
Dilatation
Humans
Magnetic Resonance Angiography
Magnetic Resonance Imaging
Perfusion
Retrospective Studies
Seizures

Figure

  • Fig. 1 A 42-year-old male patient with seizure and dysarthria (patient 13). Axial FLAIR (a) and DWI (b) show cortical hyperintensities in the right cerebral cortices (short arrows) and ipsilateral thalamus (long arrows). On ADC map image (c), the lesions (except for the insula) reveal diffusion restriction (arrows). MR angiography (d) reveals marked dilatation with increased flow signal of the right middle cerebral artery (arrows). On follow-up FLAIR (e) and DWI (f) obtained 8 months later, there is diffuse atrophy of the right cerebral hemisphere.

  • Fig. 2 A 58-year-old male patient with seizure (patient 18). Axial FLAIR (a, b) and DWI (c, d) show multiple cortical hyperintensities in the right cerebral cortices (short arrows) and ipsilateral thalamus (long arrows). ADC map images (e, f) reveal restricted water diffusion of the lesions (arrows).

  • Fig. 3 A 75-year-old female patient with aphasia (aphasic status epilepticus) (patient 21). There are hyperintense lesions in the left temporooccipital lobes, hippocampus and thalamus (arrows) on DWI (a, b). On ACD map images (c, d), the lesions show restricted diffusion (arrows). Perfusion MR images (e, f) depict increased cerebral blood flow (e) and shortened time to peak (f) in the corresponding areas (arrows). On follow-up DWI (g, h) obtained 2 days later, the extent of lesions has decreased (arrows).


Reference

1. Annegers JF. The epidemiology of epilepsy. In : Wyllie E, editor. The treatment of epilepsy: principles and practice. 3rd ed. Philadelphia: Lippincott Williams & Wilkins;2001. p. 131–138.
2. Cole AJ. Status epilepticus and periictal imaging. Epilepsia. 2004; 45:Suppl 4. 72–77.
3. Briellmann RS, Wellard RM, Jackson GD. Seizure-associated abnormalities in epilepsy: evidence from MR imaging. Epilepsia. 2005; 46:760–766.
4. Cianfoni A, Caulo M, Cerase A, et al. Seizure-induced brain lesions: a wide spectrum of variably reversible MRI abnormalities. Eur J Radiol. 2013; 82:1964–1972.
5. Davis DP, Robertson T, Imbesi SG. Diffusion-weighted magnetic resonance imaging versus computed tomography in the diagnosis of acute ischemic stroke. J Emerg Med. 2006; 31:269–277.
6. Mathews MS, Smith WS, Wintermark M, Dillon WP, Binder DK. Local cortical hypoperfusion imaged with CT perfusion during postictal Todd's paresis. Neuroradiology. 2008; 50:397–401.
7. Weinand ME, Carter LP, el-Saadany WF, Sioutos PJ, Labiner DM, Oommen KJ. Cerebral blood flow and temporal lobe epileptogenicity. J Neurosurg. 1997; 86:226–232.
8. Moritani T, Smoker WR, Sato Y, Numaguchi Y, Westesson PL. Diffusion-weighted imaging of acute excitotoxic brain injury. AJNR Am J Neuroradiol. 2005; 26:216–228.
9. Warach S, Levin JM, Schomer DL, Holman BL, Edelman RR. Hyperperfusion of ictal seizure focus demonstrated by MR perfusion imaging. AJNR Am J Neuroradiol. 1994; 15:965–968.
10. Chan S, Chin SS, Kartha K, et al. Reversible signal abnormalities in the hippocampus and neocortex after prolonged seizures. AJNR Am J Neuroradiol. 1996; 17:1725–1731.
11. Goyal MK, Sinha S, Ravishankar S, Shivshankar JJ. Peri-ictal signal changes in seven patients with status epilepticus: interesting MRI observations. Neuroradiology. 2009; 51:151–161.
12. Huang YC, Weng HH, Tsai YT, et al. Periictal magnetic resonance imaging in status epilepticus. Epilepsy Res. 2009; 86:72–81.
13. Holmes GL. Seizure-induced neuronal injury: animal data. Neurology. 2002; 59:S3–S6.
14. Wang Y, Majors A, Najm I, et al. Postictal alteration of sodium content and apparent diffusion coefficient in epileptic rat brain induced by kainic acid. Epilepsia. 1996; 37:1000–1006.
15. Kim JA, Chung JI, Yoon PH, et al. Transient MR signal changes in patients with generalized tonicoclonic seizure or status epilepticus: periictal diffusion-weighted imaging. AJNR Am J Neuroradiol. 2001; 22:1149–1160.
16. Bouilleret V, Nehlig A, Marescaux C, Namer IJ. Magnetic resonance imaging follow-up of progressive hippocampal changes in a mouse model of mesial temporal lobe epilepsy. Epilepsia. 2000; 41:642–650.
17. Szabo K, Poepel A, Pohlmann-Eden B, et al. Diffusion-weighted and perfusion MRI demonstrates parenchymal changes in complex partial status epilepticus. Brain. 2005; 128:1369–1376.
18. Nevander G, Ingvar M, Auer R, Siesjo BK. Status epilepticus in well-oxygenated rats causes neuronal necrosis. Ann Neurol. 1985; 18:281–290.
19. Toledo M, Munuera J, Sueiras M, Rovira R, Alvarez-Sabin J, Rovira A. MRI findings in aphasic status epilepticus. Epilepsia. 2008; 49:1465–1469.
20. Calistri V, Caramia F, Bianco F, Fattapposta F, Pauri F, Bozzao L. Visualization of evolving status epilepticus with diffusion and perfusion MR imaging. AJNR Am J Neuroradiol. 2003; 24:671–673.
21. Hayward NM, Ndode-Ekane XE, Kutchiashvili N, Grohn O, Pitkanen A. Elevated cerebral blood flow and vascular density in the amygdala after status epilepticus in rats. Neurosci Lett. 2010; 484:39–42.
22. Unrath A, Muller HP, Ludolph AC, Kassubek J. Reversible cortical diffusion restriction, hyperperfusion and T2-hyperintensity caused by two different types of epileptic seizure. Clin Neuroradiol. 2012; 22:239–243.
23. Zhao M, Suh M, Ma H, Perry C, Geneslaw A, Schwartz TH. Focal increases in perfusion and decreases in hemoglobin oxygenation precede seizure onset in spontaneous human epilepsy. Epilepsia. 2007; 48:2059–2067.
24. Wasterlain CG, Fujikawa DG, Penix L, Sankar R. Pathophysiological mechanisms of brain damage from status epilepticus. Epilepsia. 1993; 34:Suppl 1. S37–S53.
25. Nagasaka T, Shindo K, Hiraide M, Sugimoto T, Shiozawa Z. Ipsilateral thalamic MRI abnormality in an epilepsy patient. Neurology. 2002; 58:641–644.
26. Shipp S. The functional logic of cortico-pulvinar connections. Philos Trans R Soc Lond B Biol Sci. 2003; 358:1605–1624.
27. Katramados AM, Burdette D, Patel SC, Schultz LR, Gaddam S, Mitsias PD. Periictal diffusion abnormalities of the thalamus in partial status epilepticus. Epilepsia. 2009; 50:265–275.
28. Eid T, Ghosh A, Wang Y, et al. Recurrent seizures and brain pathology after inhibition of glutamine synthetase in the hippocampus in rats. Brain. 2008; 131:2061–2070.
29. Tuan Huynh NN, Hiroyoshi A, Shozo N, Takashi T, Hideo T, Akira M. Reversible focal radiological changes due to non-convulsive status epilepticus of the right parietooccipital lobe. Turk Neurosurg. 2013; 23:278–281.
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