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Hepatic vascular malformations in hereditary hemorrhagic telangiectasia: In search of predictors of significant disease

✍ Scribed by Guadalupe Garcia-Tsao; Karen L. Swanson


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
62 KB
Volume
48
Category
Article
ISSN
0270-9139

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We read with interest the article by Mitchell et al. 1 dealing with bevacizumab treatment of a patient with hereditary hemorrhagic telangiectasia (HHT), cardiac failure, and portal hypertension due to severe liver vascular malformations (VMs). The treatment reversed the need for liver transplantatio