Abstract:
Hereditary haemorrhagic telangiectasia (HHT) is a rare autosomal dominant disorder with mucocutaneous
telangiectasias and arteriovenous malformations (AVM). We report an asymptomatic patient with a pulmonary
AVM (PAVM) found on routine imaging. He later disclosed recurrent childhood epistaxis and a family history
suggestive of HHT. Imaging studies confirmed a large PAVM without other organ involvement. Early diagnosis and transcatheter embolisation helped prevent severe complications like stroke and haemorrhage. This case
highlights the importance of exclusion of HHT as an important cause of an unexplained pulmonary shadow.
