Hereditary hemorrhagic telangiectasia in children: endovascular treatment of neurovascular malformations
β Scribed by T. Krings; S.M. Chng; A. Ozanne; H. Alvarez; G. Rodesch; P.L. Lasjaunias
- Publisher
- Springer
- Year
- 2005
- Tongue
- English
- Weight
- 406 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0028-3940
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
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
## Abstract ## Objectives/Hypothesis: Determine the effectiveness of treating epistaxis in hereditary hemorrhagic telangiectasia (HHT) with potassium titanyl phosphate (KTP) laser cautery combined with submucosal injection of 100 mg of bevacizumab. ## Study Design: Retrospective pilot study. ##