Volume 45, Issue 6 pp. 686-689

Regional Cerebral Hyperperfusion with Ictal Dystonic Posturing: Ictal–Interictal SPECT Subtraction

Eun Yeon JooSeung Bong Hong

Seung Bong Hong

Neurology

Neuroimaging Laboratory of Neurology, Samsung Medical Center & Center for Clinical Medicine, SBRI, Sungkyunkwan University School of Medicine

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Eun Kyung Lee

Eun Kyung Lee

Neuroimaging Laboratory of Neurology, Samsung Medical Center & Center for Clinical Medicine, SBRI, Sungkyunkwan University School of Medicine

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Woo Suk Tae

Woo Suk Tae

Neurology

Neuroimaging Laboratory of Neurology, Samsung Medical Center & Center for Clinical Medicine, SBRI, Sungkyunkwan University School of Medicine

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Jee Hyun KimDae Won SeoSeung Chyul Hong

Seung Chyul Hong

Neurosurgery

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Seunghwan Kim

Seunghwan Kim

APCTP/NCSL, Department of Physics, POSTECH, Pohang, Korea

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Myoung-Hee Kim

Myoung-Hee Kim

Department of Computer Science and Engineering, Ewha Womans University, Seoul, Korea

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First published: 14 May 2004
Citations: 33
Address correspondence and reprint requests to Dr. S.B. Hong at Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50 Irwon-Dong, Gangnam-Gu, Seoul, 135-710, Korea. E-mail: [email protected]

Abstract

Summary:  Purpose: Ictal–interictal single-photon emission computed tomography (SPECT) subtraction was performed to find brain structures related to ictal dystonic posturing (DP) in patients with temporal lobe epilepsy (TLE).

Methods: Thirty-two patients with mesial TLE who had ictal and interictal SPECTs were included. They were divided into two groups; DP group with ictal dystonia during ictal SPECT (n = 15) and Non-DP group without ictal DP (n = 17). Ictal–interictal SPECT subtraction was performed, and then subtracted SPECT was coregistered with brain spoiled gradient recalled (SPGR) magnetic resonance imaging (MRI). The ictal hyperperfusion on subtracted SPECT was analyzed in basal ganglia, frontal cortex, thalamus, temporal lobe, and insular cortex.

Results: The incidences of ictal hyperperfusion on brain regions in DP versus Non-DP groups were 80.0% (12 of 15 patients) versus none (0 of 17), p = 0.001, χ2, in caudate nucleus; 93.3% (14 of 15) versus 47.0% (eight of 17), p = 0.005, in putamen; and 80.0% (12 of 15) versus 41.2% (seven of 17), p = 0.026, in thalamus. No significant difference of ictal hyperperfusion was found in globus pallidus, temporal lobes, insular and frontal cortices between DP and Non-DP groups. DP patients showed an earlier age at seizure onset [8.6 years (DP) vs. 15.7 years (Non-DP) (p = 0.015)] and a longer duration of seizure history [19.0 years (DP) vs. 11.9 years (Non-DP) (p = 0.015)].

Conclusions: Caudate nucleus, putamen, and thalamus were significantly related to the ictal DP during TLE seizures. Our study showed first an active involvement of the caudate nucleus in the generation of ictal DP.

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