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Japanese

OSLER'S DISEASE WITH BILATERAI PULMONARY ARTERIO-VENOUS FISTULAE Yu Masuda 1 pp.197-201
Published Date 1976/3/20
DOI https://doi.org/10.11477/mf.1492208323
  • Abstract
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 A case of hereditary hemorrhagic teleangiectasis in a woman, aged 37, is reported. The patient complained of a repeated epistaxis for the period 2 months. The treatment by means of electrocoagulation was effective for only a week.

 The chest x-ray examination revealed an abnormal shadow in the left lower lobe.

 Further examination revealed teleangiectasis on the nasal mucous membrane, lips and tongue. The pulmonary and celiac angiographies revealed bilateral pulmonary arteriovenous fistulas and multiple angiostatic abnormalities in the liver. Operative treatment was impossible.

 The patient was treated by administration of anticoagulant drugs and local applications of electrocoagulations.

 A recent examination showed the patient remarkably improved in her general condition and a stop in the nasal bleeding.


Copyright © 1976, 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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