Summary:
Hereditary Hemorrhagic Telangiectasia (HHT), also known
as Osler-Weber-Rendu Syndrome, is an autosomal
dominant disorder. The typical findings of the disease are
telangiectasias in skin and mucous membranes and
arteriovenous malformations and aneurysms presenting in
the organs like brain, lung, intestine and liver. The most
common symptoms are recurrent epistaxis and
gastrointestinal bleeding.
We report here a case of 38-year-old male who presented
with typical history of recurrent epistaxis, hematemesis and