Hereditary hemorrhagic telangiectasia (HHT) is a predominantly inherited disorder of blood vessel structure, characterized by mucocutaneous telangiectasias, multiple arteriovenous malformations, and frequent epistaxis. A 67-year-old female with atrial fibrillation and high thromboembolic risk (CHADs2Vasc2: 4) with renal arterial thrombosis started oral anticoagulation (OAC). The patient had multiple episodes of heavy nasal and gastrointestinal bleeding (requiring multiple blood transfusions) such that OAC had to be interrupted, and a complementary investigation led to the diagnosis of HHT. Due to concomitant high thromboembolic and hemorrhagic risks, the patient was proposed left atrial appendage occlusion as an alternative to OAC intolerance. After the procedure, there were no new episodes of bleeding or thrombotic events.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8249143PMC
http://dx.doi.org/10.7759/cureus.15367DOI Listing

Publication Analysis

Top Keywords

left atrial
8
atrial appendage
8
appendage occlusion
8
atrial fibrillation
8
hereditary hemorrhagic
8
hemorrhagic telangiectasia
8
high thromboembolic
8
occlusion therapeutic
4
therapeutic option
4
option patient
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!