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Japanese

A CASE OF BILATERAL STURGE-WEBER'S DISEASE WITH A PLEXUSPILLOMA AT THE LEFT LATERAL VENTRICLE Yuji Hamanaka 1 , Shintaro Mori 1 , Mitsumasa Kanoh 1 , Tohru Uozumi 1 , Kenzo Matsuoka 1 , Emiko inoue 2 , Hiroshi Yokoi 3 , Sukeo Yoshitatsu 3 11st Dept. Surg., Osaka University Medical School 2Dept. Pediatrics, Osaka University Medical School 3Dept. Surg., Osaka Nissei Hospital pp.99-103
Published Date 1970/1/1
DOI https://doi.org/10.11477/mf.1406202665
  • Abstract
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A ten-month-old boy was reported who was noted a port-wine nevi on the left side of the forehead at birth. At four months of age, he had convulsions of the right arm and leg, and admitted to our hospital at ten months.

On examination, hemiparesis of the right arm and leg were recongnized. An electroencephalogram showed spike and wave-complex on the left occipital region. Intracranial calcification was not visible on x-ray film, but cortical atrophy was suggested by cerebral angiography and a round tumor shadow at the trigone of the left lateral ventricle by pneu-moencephalography.

When the right ventricular drainage and the left temporo-parieto-occipital craniotomy were done, venous angioma of the leptomeninges were revealed. After the opening of the left ventricle, a round red-dish tumor was found and totally extirpated.

Histologically the tumor was a typical papilloma of the choroid plexus. No malignant cells were found.

The patient was discharged without convulsion.


Copyright © 1970, 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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