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Japanese

OSLER'S DISEASE HEREDITARY HEMORRHAGIC TELANGIECTASIA Rokuro Kawano 1 pp.571-578
Published Date 1973/8/20
DOI https://doi.org/10.11477/mf.1492207948
  • Abstract
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 A case of Osler's disease in a woman, aged 72 is reported. The personal history revealed the patient affected with repeated epistaxis since her childhood but, recently, since a few years ago the hemorrhage had been profuse as to necessiate hospitalization. The hereditary influence was not conclusive.

 The telangiectasis is found in other areas of the body, such as, lips, tongue, the mucous membranes of the mouth, nose and stomach and in parts of the fingers.

 The growth on the inferior turbinate was treated by cauterization which was deemed inapplicable to those on the nasal septum. The latter was treated by means of estrogen therapy which appeared to be successful. At present, 2 months later there is no hemorrhage.


Copyright © 1973, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 印刷版ISSN 0386-9679 医学書院

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