Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add filters








Language
Year range
1.
Korean Journal of Otolaryngology - Head and Neck Surgery ; : 613-619, 2016.
Article in Korean | WPRIM | ID: wpr-645985

ABSTRACT

Hereditary hemorrhagic telangiectasia (HHT) is a hereditary, autosomal dominant, vascular dysplasia characterized by mucocutaneous telangiectasia, epistaxis, gastrointestinal bleeding, and iron deficiency anemia. Epistaxis in HHT is a recurrent and debilitating symptom, which is difficult to manage. Many methods have been tried with little success. Bevacizumab (Avastin®), a VEGF inhibitor, has been recently tried intranasally or systemically to control the recurrent epistaxis. We report three patients with HHT who were treated with intranasal bevacizumab application together with cauterization. In all three patients, recurrent epistaxis decreased considerably with improvement in quality of life. Here we describe the application methods, treatment results, and complications with literature review. We believe that this is the first report of treating epistaxis in HHT with intranasal application of bevacizumab in South Korea.


Subject(s)
Humans , Anemia, Iron-Deficiency , Bevacizumab , Cautery , Epistaxis , Hemorrhage , Korea , Quality of Life , Telangiectasia, Hereditary Hemorrhagic , Telangiectasis , Vascular Endothelial Growth Factor A
SELECTION OF CITATIONS
SEARCH DETAIL