Literature DB >> 18409543

[Ictal Gerstmann's syndrome in a patient with symptomatic parietal lobe epilepsy].

Akihiro Shimotake1, Youshi Fujita, Akio Ikeda, Hidekazu Tomimoto, Jun Takahashi, Ryosuke Takahashi.   

Abstract

A 34-year-old man with astrocytoma in the left parietal lobe had symptomatic partial epilepsy, and he presented transient episodes of acalculia, agraphia and finger agnosia. Occasionally he had difficulty in finding appropriate letters when making an e-mail, and difficulty in writing and calculation. Neurological examinations revealed ictal symptoms of Gerstmann's syndrome without right to left disorientation. No other higher cortical dysfunction or neurological deficits were noted. Scalp EEGs showed frequent, regional ictal discharges in the left parietal area lasting for 60-240 seconds. These clinico-electrographical observations strongly support that epileptic seizures produced a loss of cortical higher function manifesting Gerstmann's syndrome.

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Year:  2008        PMID: 18409543     DOI: 10.5692/clinicalneurol.48.208

Source DB:  PubMed          Journal:  Rinsho Shinkeigaku        ISSN: 0009-918X


  1 in total

1.  Ictal conduction aphasia and ictal angular gyrus syndrome as rare manifestations of epilepsy: The importance of ictal testing during video-EEG monitoring.

Authors:  Johann Philipp Zöllner; Anja Haag; Anke Hermsen; Sebastian Bauer; Friederike Stahl; Karina Wulf; Katja Menzler; Philipp S Reif; Marlies Wagner; Axel Pagenstecher; Ulrich Sure; Susanne Knake; Felix Rosenow; Adam Strzelczyk
Journal:  Epilepsy Behav Case Rep       Date:  2017-08-03
  1 in total

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