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  • Title: Gastric predominant hereditary hemorrhagic telangiectasia.
    Author: Katsinelos P, Chatzimavroudis G, Zavos C, Kamperis E, Triantafillidis I, Pilpilidis I, Katsinelos T, Papaziogas B.
    Journal: Vasa; 2006 Nov; 35(4):258-61. PubMed ID: 17109371.
    Abstract:
    Hereditary hemorrhagic telangiectasia (HHT) or Rendu-Osler-Weber disease is an autosomal-dominant disorder that frequently presents with epistaxis and gastrointestinal bleeding which may be a diagnostic and therapeutic challenge. We describe a 48-year-old monk with familiar history of HHT, who presented with frequent epistaxes and symptoms of ferropenic anemia. Upper gastrointestinal endoscopy revealed innumerable telangiectasias in the stomach. The patient underwent three sessions with argon plasma coagulation treatment but the results were poor. We also review the literature on the pathophysiology of the disease and discuss the suggested treatment.
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