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Research ArticleBrain

MRI Findings in Autoimmune Voltage-Gated Potassium Channel Complex Encephalitis with Seizures: One Potential Etiology for Mesial Temporal Sclerosis

A.L. Kotsenas, R.E. Watson, S.J. Pittock, J.W. Britton, S.L. Hoye, A.M.L. Quek, C. Shin and C.J. Klein
American Journal of Neuroradiology January 2014, 35 (1) 84-89; DOI: https://doi.org/10.3174/ajnr.A3633
A.L. Kotsenas
aFrom the Departments of Radiology (A.L.K., R.E.W., S.L.H.)
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R.E. Watson
aFrom the Departments of Radiology (A.L.K., R.E.W., S.L.H.)
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S.J. Pittock
bNeurology (S.J.P., J.W.B., A.M.L.Q., C.S., C.J.K.)
cLaboratory Medicine and Pathology (S.J.P., C.J.K.), Mayo Clinic, Rochester Minnesota
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J.W. Britton
bNeurology (S.J.P., J.W.B., A.M.L.Q., C.S., C.J.K.)
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S.L. Hoye
aFrom the Departments of Radiology (A.L.K., R.E.W., S.L.H.)
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A.M.L. Quek
bNeurology (S.J.P., J.W.B., A.M.L.Q., C.S., C.J.K.)
dDepartment of Medicine (A.M.L.Q.), National University Health System, Singapore.
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C. Shin
bNeurology (S.J.P., J.W.B., A.M.L.Q., C.S., C.J.K.)
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C.J. Klein
bNeurology (S.J.P., J.W.B., A.M.L.Q., C.S., C.J.K.)
cLaboratory Medicine and Pathology (S.J.P., C.J.K.), Mayo Clinic, Rochester Minnesota
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Abstract

BACKGROUND AND PURPOSE: Autoimmune voltage-gated potassium channel complex encephalitis is a common form of autoimmune encephalitis. Patients with seizures due to this form of encephalitis commonly have medically intractable epilepsy and may require immunotherapy to control seizures. It is important that radiologists recognize imaging characteristics of this type of autoimmune encephalitis and suggest it in the differential diagnosis because this seizure etiology is likely under-recognized. Our purpose was to characterize MR imaging findings in this patient population.

MATERIALS AND METHODS: MR imaging in 42 retrospectively identified patients (22 males; median age, 56 years; age range, 8–79 years) with seizures and voltage-gated potassium channel complex autoantibody seropositivity was evaluated for mesial and extratemporal swelling and/or atrophy, T2 hyperintensity, restricted diffusion, and enhancement. Statistical analysis was performed.

RESULTS: Thirty-three of 42 patients (78.6%) demonstrated enlargement and T2 hyperintensity of mesial temporal lobe structures at some time point. Mesial temporal sclerosis was commonly identified (16/33, 48.5%) at follow-up imaging. Six of 9 patients (66.7%, P = .11) initially demonstrating hippocampal enhancement and 8/13 (61.5%, P = .013) showing hippocampal restricted diffusion progressed to mesial temporal sclerosis. Conversely, in 6 of 33 patients, abnormal imaging findings resolved.

CONCLUSIONS: Autoimmune voltage-gated potassium channel complex encephalitis is frequently manifested as enlargement, T2 hyperintensity, enhancement, and restricted diffusion of the mesial temporal lobe structures in the acute phase. Recognition of these typical imaging findings may help prompt serologic diagnosis, preventing unnecessary invasive procedures and facilitating early institution of immunotherapy. Serial MR imaging may demonstrate resolution or progression of radiologic changes, including development of changes involving the contralateral side and frequent development of mesial temporal sclerosis.

ABBREVIATIONS:

Ab
autoantibody
CASPR2
contactin-associated protein-like 2
LGI1
leucine-rich glioma-inactivated protein 1
MTS
mesial temporal sclerosis
VGKC
voltage-gated potassium channel complex
  • © 2014 by American Journal of Neuroradiology
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American Journal of Neuroradiology: 35 (1)
American Journal of Neuroradiology
Vol. 35, Issue 1
1 Jan 2014
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Cite this article
A.L. Kotsenas, R.E. Watson, S.J. Pittock, J.W. Britton, S.L. Hoye, A.M.L. Quek, C. Shin, C.J. Klein
MRI Findings in Autoimmune Voltage-Gated Potassium Channel Complex Encephalitis with Seizures: One Potential Etiology for Mesial Temporal Sclerosis
American Journal of Neuroradiology Jan 2014, 35 (1) 84-89; DOI: 10.3174/ajnr.A3633

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MRI Findings in Autoimmune Voltage-Gated Potassium Channel Complex Encephalitis with Seizures: One Potential Etiology for Mesial Temporal Sclerosis
A.L. Kotsenas, R.E. Watson, S.J. Pittock, J.W. Britton, S.L. Hoye, A.M.L. Quek, C. Shin, C.J. Klein
American Journal of Neuroradiology Jan 2014, 35 (1) 84-89; DOI: 10.3174/ajnr.A3633
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Cited By...

  • Mesiotemporal Volumetry, Cortical Thickness, and Neuropsychological Deficits in the Long-term Course of Limbic Encephalitis
  • Clinical Course and Features of Seizures Associated With LGI1-Antibody Encephalitis
  • Network-wide abnormalities explain memory variability in hippocampal amnesia
  • Rapidly progressive global cerebral atrophy in the setting of anti-LGI1 encephalitis
  • Beyond the limbic system: disruption and functional compensation of large-scale brain networks in patients with anti-LGI1 encephalitis
  • LGI1, CASPR2 and related antibodies: a molecular evolution of the phenotypes
  • Autoimmune Encephalitis: Pathophysiology and Imaging Review of an Overlooked Diagnosis
  • Anti-LGI1 encephalitis: Clinical syndrome and long-term follow-up
  • Neuronal autoantibodies in mesial temporal lobe epilepsy with hippocampal sclerosis
  • Recognizing Autoimmune-Mediated Encephalitis in the Differential Diagnosis of Limbic Disorders
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