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Familial Occurrence of Intracerebral Cavernous Angioma:Report of cases in brothers Kunio YAMAMURA 1 , Hiroshi KAJIKAWA 1 , Manabu WADA 1 , Minako KAJIKAWA 1 , Shinya SUMIOKA 1,2 , Yoshio SUYAMA 1,2 , Fumio SHIMAMOTO 3 1Section of Neurosurgery, Suiseikai Kajikawa Hospital 2Department of Neurosurgery, Osaka Medical College 3Division of Pathology, Hiroshima University Hospital Keyword: Cavernous angioma , Familial occurrence pp.1105-1109
Published Date 1995/12/10
DOI https://doi.org/10.11477/mf.1436901128
  • Abstract
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Familial occurrence of intracerebral cavernous angioma has been rerely reported. We report two histo-logically verified cases of cavernous angioma among brothers and review relevant cases in the literature.

Case 1 is that of a 3-year-old boy who suffered from acute onset of headache, vomiting, and tonic-clonic type seizure. CT revealed a well-demarcated tumor with par-tial hemorrhage in the left frontal lobe which was strongly enhanced with contrast medium. Complete ex-cision was carried out and the patient had a satisfactory clinial course and was able to be followed up for 13 years after the surgery. Case 2 is that of a 17-year-old boy who was the elder brother of case 1 and presented with gradually increasing episodes of a pyschomotor seizure which started at the age of 16.

CT and MRI revealed a well-demarcated tumor in the left subcortical temporal lobe and an asymptomatic small calcified lesion in the left subcortical parietal lobe. The temporal tumor was totally excised and histo-logically diagnosed as cavernous angioma. The seizures gradually decreased and eventually disappeared one year after the surgery.

This report reviews 13 previously reported cases and surgical indication for asymptomatic cases.


Copyright © 1995, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1251 印刷版ISSN 0301-2603 医学書院

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