Pulmonary hypertension and hepatic encephalopathy: lethal complications of Rendu-Osler-Weber disease

Ford, T. J. , Fong, M.W., Cheah, B.C. and Alexopolous, C. (2014) Pulmonary hypertension and hepatic encephalopathy: lethal complications of Rendu-Osler-Weber disease. Journal of the Royal College of Physicians of Edinburgh, 44(2), pp. 126-129. (doi: 10.4997/JRCPE.2014.207) (PMID:24999773)

Full text not currently available from Enlighten.

Abstract

Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disorder characterised by epistaxis, mucocutaneous telangiectasia with systemic manifestations due to visceral telangiectasia and arterio-venous malformations (AVMs). We describe unusual complications of HHT in a 68-year-old male who developed high-output cardiac failure with pulmonary hypertension in combination with hepatic encephalopathy due to hepatic AVMs. This case shows the importance of a multi-system approach to HHT and considers the treatment of its hepatic complications.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Ford, Thomas
Authors: Ford, T. J., Fong, M.W., Cheah, B.C., and Alexopolous, C.
College/School:College of Medical Veterinary and Life Sciences > School of Cardiovascular & Metabolic Health
Journal Name:Journal of the Royal College of Physicians of Edinburgh
Publisher:Royal College of Physicians of Edinburgh
ISSN:1478-2715
ISSN (Online):2042-8189

University Staff: Request a correction | Enlighten Editors: Update this record