Internal Medicine
Online ISSN : 1349-7235
Print ISSN : 0918-2918
ISSN-L : 0918-2918
Hereditary Hemorrhagic Telangiectasia Showing Severe Anemia which was Successfully Treated with Estrogen
Takeshi HISADAHidemasa KUWABARATakeshi TSUNODAKaori KANEKOShouzou KUBOTAYoshihiro MIWAMasatomo MORI
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JOURNAL FREE ACCESS

1995 Volume 34 Issue 6 Pages 589-592

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Abstract

Hereditary hemorrhagic telangiectasia (Osier-Weber-Rendu disease) is a bleeding disorder attributed to a vascular developmental abnormality. It is transmitted as an autosomal dominant trait. A 63-year-old female was admitted because of repeated episodes of severe anemia which resulted from bleeding of telangiectases in the gastric mucosa. Conventional therapies including endoscopical microwave coagulation and ethanol injection were not effective. The persistent anemia necessitated frequent blood transfusion. Estrogen was orally administrated and blood transfusion became unnecessary. Thus, estrogen therapy should be considered as one of the effective treatments for recurrent severe anemia due to hereditary hemorrhagic telangiectasia.
(Internal Medicine 34: 589-592, 1995)

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