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

Détails

ID Serval
serval:BIB_D2712C37DB27
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Etude de cas (case report): rapporte une observation et la commente brièvement.
Collection
Publications
Titre
Fatal hypoxic hepatitis in a patient with hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber's disease).
Périodique
Acta Gastro-enterologica Belgica
Auteur⸱e⸱s
Henrion J., Deltenre P., Peny M.O., Dumoulin P., Laurent Y., Brenard R.
ISSN
0001-5644 (Print)
ISSN-L
0001-5644
Statut éditorial
Publié
Date de publication
2010
Volume
73
Numéro
1
Pages
61-64
Langue
anglais
Notes
Publication types: Case Reports ; Journal ArticlePublication Status: ppublish
Résumé
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 therapeutic ligation or embolization of the hepatic artery so as to decrease shunting of liver blood. Hemodynamic mechanisms are proposed to explain this particular outcome.
Mots-clé
Anoxia/diagnosis, Anoxia/etiology, Fatal Outcome, Female, Hepatitis/diagnosis, Hepatitis/etiology, Humans, Ischemia/diagnosis, Ischemia/etiology, Middle Aged, Telangiectasia, Hereditary Hemorrhagic/complications, Telangiectasia, Hereditary Hemorrhagic/pathology
Pubmed
Web of science
Création de la notice
06/12/2013 11:11
Dernière modification de la notice
20/08/2019 16:52
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