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TWO CASES OF EPILEPSY WITH SALIVARY SEIZURES Hosaku Torii 1 , Minoru Hayashi 1 , Yasuo Shimazono 1 1Dept. of Neuropsychiatry, Kanazawa University School of Medicine pp.783-792
Published Date 1963/8/1
DOI https://doi.org/10.11477/mf.1406201521
  • Abstract
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The clinical findings of 2 patients with sa-livary seizure, which, if not accompanied by automatism convulsion or other symptoms, is regarded as a relatively rare type of epileptic seizures, are reported.

Case 1. A 33-year-old housewife has suf-fered from salivary seizures since 8 years, and automatism accompanied by salivation began to appear 3 years ago. One of three her children is an epileptic with psychomotor seizures. In EEG, localized paroxysmal dis-charges were not found at rest, and irregular spikes and diffuse spindle burst were seen in asleep state. I. Q. was 70 to 80. Administra-tion of adrenalin always provoked almost the same automatism as occured spontaneously, and 5 to 6 per sec. generalized high voltage slow waves were recorded during the auto-matism. She had Ichthyosis vulgaris and Ade-noma sebaceum, the latter being ascertained by histological study.

Case 2. A 16-year-old male student has shown salivary seizures and convulsive seizu-res separately since one year. One of his cousins has suffered from convulsive seizures. EEG findings in asleep state were similer to those in Case 1.

Brain structurs to be related to salivary seizure, EEG findings during automatism, pro-vokation of automatism by administration of adrenalin and complication of dermatological diseases are discussed.


Copyright © 1963, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 2185-405X 印刷版ISSN 0006-8969 医学書院

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