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Updated: Jun 17, 2026

A Patient-Derived Xenograft Model for Venous Malformation
Published on: June 15, 2020
Hereditary hemorrhagic telangiectasia/avastin
Terence M Davidson1, Scott E Olitsky, Julie L Wei
1Department of Head and Neck Surgery, San Diego School of Medicine, University of California, VA San Diego Healthcare System, San Diego, California 92161, USA. tdavidson@ucsd.edu
Intranasal bevacizumab (Avastin), a VEGF inhibitor, offers a novel treatment for hereditary hemorrhagic telangiectasia (HHT) related nosebleeds. This topical spray effectively reduces epistaxis in HHT patients, improving management of this serious condition.
Area of Science:
- Vascular biology and regenerative medicine
- Otolaryngology and medical research
Background:
- Hereditary hemorrhagic telangiectasia (HHT) causes difficult-to-manage epistaxis due to nasal telangiectasias.
- Vascular Endothelial Growth Factor (VEGF) plays a key role in the development of these vascular malformations.
- Current treatments for HHT epistaxis are often invasive and unpleasant for patients.
Observation:
- This study reports the first use of intranasal bevacizumab (Avastin) for HHT epistaxis.
- Bevacizumab is a VEGF inhibitor that targets the underlying pathology of HHT.
- Topical application via nasal spray offers a new route of administration.
Findings:
- Intranasal bevacizumab spraying effectively reduced epistaxis in patients with HHT.
- The topical VEGF inhibitor demonstrated efficacy in managing severe nosebleeds.
- This method provides a less invasive treatment option compared to systemic or local injections.
Implications:
- Intranasal bevacizumab represents a promising, minimally invasive therapeutic strategy for HHT.
- This approach could significantly improve the quality of life for HHT patients suffering from epistaxis.
- Further research into topical VEGF inhibition may reveal broader applications in vascular disorders.
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