Embolization of a Duodenal Arteriovenous Malformation in Hereditary Hemorrhagic Telangiectasia: Case Report and Review of the Literature

Author:

Inouye Phil1,Marcon Norman2,Pugash Robin A3,Hyland Robert H4,Faughnan Marie E45

Affiliation:

1. Department of Medicine, University of Toronto, Canada

2. Division of Gastroenterology, Department of Medicine, St Michael’s Hospital, University of Toronto, Canada

3. Department of Medical Imaging, University of Toronto, Department of Medical Imaging, Sunnybrook and Women’s College Health Sciences Centre, Canada

4. Division of Respiratory Medicine, Department of Medicine, St Michael’s Hospital, University of Toronto, Canada

5. Financial Support, Squires Club, Nelson Arthur Hyland Foundation, Sonor Foundation, St Michael’s Hospital Research Institute, Toronto, Ontario, Canada

Abstract

A 68-year-old man with hereditary hemorrhagic telangiectasia presented with recurrent, intermittent gastrointestinal hemorrhage. Transfusion of a total of 27 units of red blood cells was required over the three months before admission. Upper and lower endoscopy did not reveal a source of bleeding and a technetium-labelled red blood cell scan was noncontributory. Angiography demonstrated a duodenal arteriovenous malformation originating from a superior mesenteric artery branch. Embolization of the arteriovenous malformation was performed with resolution of gastrointestinal hemorrhage and reduced requirement for blood transfusion. The utility of trans-catheter embolization in the management of duodenal arteriovenous malformations in hereditary hemorrhagic telangiectasia is discussed.

Publisher

Hindawi Limited

Subject

Gastroenterology,General Medicine

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