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A CASE OF BILATERAL STURGE-WEBER SYNDROME Tohru YABE 1 , Reijin HABA 2 1Neuropsychiatric Research Institute 2Dept. of Psychiatry, Ome City Hospital pp.1137-1142
Published Date 1966/11/1
DOI https://doi.org/10.11477/mf.1406202136

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  • Abstract
  • Look Inside

A man, born in 1941.

There was nothing of note in the family history. Born at term, he was normal except for bilateral facial naevi flammei on the distribution area of 1 st, 2 nd and the upper two-thirds of 3 rd branch of the trigeminal nerve, almost symmetrically except small spots of naevi scattered in the mandible and lateral neck on the right side.

The mucosa of soft palate was hyperemic diffusely.

The conjunctiva in the both eyes were hyperemic, with an excess of fine vessels. The patient had an operation for right glaucoma at the age of nine, and lost the sight of right eye due to cataracts complicata. The left ocular tension showed 14. 5 mmHg, although optic disk was pale and excavated on its nasal side, demonstrated atrophy.

The first attack of convulsions was at the age of 12 months, and after an interval of six years convul-sions had appeared in Jacksonian type started from right foot.

Electroencphalographically the low voltage pattern was noticed, and a waves were observed only in right occipital region.

Radiological examination revealed string-shaped cla-cification located in the parieto-occipital portion on the both sides of the skull.

His mental development was retarded, and he could not help to leave school at the age of nine. The re-sults of the intelligence test revealed I. Q. 45.

From these findings, the bilateral Sturge-Weber Syndrome was confirmed.


Copyright © 1966, 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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