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Fatal hypoxic hepatitis in a patient with hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber's disease)

Journal Volume 73 - 2010
Issue Fasc.1 - Case reports
Author(s) J. Henrion, P. Deltenre, M.-O. Peny, Ph. Dumoulin, Y. Laurent, R. Brenard
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(1) Unité d'Hépatogastroentérologie ; (2) Service d'Anatomopathologie ; (3) Service de Radiologie ; (4) Service de Réanimation, Hôpital de Jolimont, Haine-Saint-Paul, B-7100, Belgium ; (5) Service d'Hépatogastroentérologie, Grand Hôpital de Charleroi, Site St Joseph, Gilly, B-6060, Belgium.

Hypoxic (ischemic) hepatitis generally requires the concurrence of an underlying condition which chronically exposes the liver to some degree of hypoxia (for example, congestive heart failure) combined with a triggering event (for example, arrhythmia) which further decreases the oxygen supply. We report a case of hypoxic hepatitis in which hereditary hemorrhagic telangiectasia (Rendu- Osler-Weber's disease) constituted this underlying condition and gastrointestinal hemorrhage was the triggering event. To our knowledge, this is the first reported case of hypoxic hepatitis in hereditary hemorrhagic telangiectasia with the exception of thera- peutic ligation or embolization of the hepatic artery so as to decrease shunting of liver blood. Hemodynamic mechanisms are proposed to explain this particular outcome. (Acta gastroenterol. belg., 2010, 73, 61-64).

© Acta Gastro-Enterologica Belgica.
PMID 20458853