| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5811671 | Medical Hypotheses | 2014 | 4 Pages |
BackgroundHereditary hemorrhagic telangiectasia (HHT) and hepatopulmonary syndrome are disorders characterized by the development of multiple pulmonary arteriovenous malformations (PAVM).Presentation of the hypothesisCOX2 may be at the origin of a cascade of pro inflammatory events to favour angiogenesis and PAVM development.Testing the hypothesisHHT and hepatopulmonary syndrome mouse models may be used to show its effects on PAVM formation. Anti COX-2 therapy could also be tested in human individuals, particularly in patients presenting a hepatopulmonary syndrome or HHT with small PAVM.Implication of the hypothesisPAVMs are one of the main causes of morbidity in patients presenting with HHT disease, owing to the risks of rupture as well as paradoxical embolism exposing to stroke and/or cerebral abscess. Percutaneous embolization has become the treatment of choice of PAVM. Anti COX2 may prevent from PAVM development and subsequent related complications and avoid either surgery and/or percutaneous embolization and thus subsequent related complication.
