Literature DB >> 9869617

Liver transplantation resolves the hyperdynamic circulation in hereditary hemorrhagic telangiectasia with hepatic involvement.

O Boillot1, F Bianco, J P Viale, F Mion, I Mechet, D Gille, J Delaye, P Paliard, H Plauchu.   

Abstract

BACKGROUND & AIMS: Hepatic involvement in hereditary hemorrhagic telangiectasia is common but often asymptomatic. However, in some cases, the vascular lesions that involve the liver may lead to high-output cardiac failure and pulmonary hypertension that is predominant over hepatobiliary manifestations. Liver transplantation and treatment of these complications are described and discussed in this article.
METHODS: Three patients with hereditary hemorrhagic telangiectasia and hepatic involvement received transplants. They had pulmonary hypertension and chronic right-sided heart failure caused by disseminated intrahepatic telangiectasias with shunts between the hepatic artery and hepatic veins or portal vein. Left-to-right intrahepatic shunt output was estimated to range between 51% and 57.5% of cardiac output.
RESULTS: Hyperdynamic circulation disappeared after liver transplantation in all patients. Results of computed tomography and right-sided heart catheterization performed 6 months later were normal. Follow-up periods currently are 65, 53, and 29 months, and each patient continues to be asymptomatic.
CONCLUSIONS: This report suggests that liver transplantation can be considered as an alternative and successful curative treatment that may prevent the irreversible evolution of cardiopulmonary disease.

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Mesh:

Year:  1999        PMID: 9869617     DOI: 10.1016/s0016-5085(99)70243-x

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


  15 in total

1.  Hepatic arteriovenous malformations from hereditary hemorrhagic telangiectasia: treatment with liver transplantation.

Authors:  Maximilian Lee; Daniel Y Sze; C Andrew Bonham; Tami J Daugherty
Journal:  Dig Dis Sci       Date:  2010-09-16       Impact factor: 3.199

2.  Abnormal pulmonary density discovered on routine chest radiograph.

Authors:  A B Small
Journal:  Proc (Bayl Univ Med Cent)       Date:  2001-01

3.  [64-year old patient with tachycardia and signs of heart failure].

Authors:  M M Zaruba; T Waggershauser; S Weckbach; A Gerbes; O Mühling; S Kääb
Journal:  Internist (Berl)       Date:  2009-04       Impact factor: 0.743

4.  Successful liver transplantation for Rendu-Weber-Osler disease, a single centre experience.

Authors:  Murat Cag; Maxime Audet; Anne-Catherine Saouli; Murad Odeh; Bernard Ellero; Tullio Piardi; Marie-Lorraine Woehl-Jaeglé; Jacques Cinqualbre; Philippe Wolf
Journal:  Hepatol Int       Date:  2011-02-17       Impact factor: 6.047

5.  Conditional knockout of activin like kinase-1 (ALK-1) leads to heart failure without maladaptive remodeling.

Authors:  Kevin J Morine; Xiaoying Qiao; Vikram Paruchuri; Mark J Aronovitz; Emily E Mackey; Lyanne Buiten; Jonathan Levine; Keshan Ughreja; Prerna Nepali; Robert M Blanton; Richard H Karas; S Paul Oh; Navin K Kapur
Journal:  Heart Vessels       Date:  2017-02-17       Impact factor: 2.037

6.  Hepatic artery embolization for treatment of patients with hereditary hemorrhagic telangiectasia and symptomatic hepatic vascular malformations.

Authors:  Ajay Chavan; Martin Caselitz; Karl-Friedrich Gratz; Joachim Lotz; Timm Kirchhoff; Plinio Piso; Siegfried Wagner; Michael Manns; Michael Galanski
Journal:  Eur Radiol       Date:  2004-08-17       Impact factor: 5.315

7.  Treatment of high output cardiac failure by flow-adapted hepatic artery banding (FHAB) in patients with hereditary hemorrhagic telangiectasia.

Authors:  A Koscielny; W A Willinek; A Hirner; M Wolff
Journal:  J Gastrointest Surg       Date:  2007-11-20       Impact factor: 3.452

8.  Massive haemoptysis after living donor liver transplantation.

Authors:  P Aseni; M Vertemati; E Minola; E Bonacina
Journal:  J Clin Pathol       Date:  2003-11       Impact factor: 3.411

Review 9.  Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): a view from the 21st century.

Authors:  M E Begbie; G M F Wallace; C L Shovlin
Journal:  Postgrad Med J       Date:  2003-01       Impact factor: 2.401

10.  Hereditary Hemorrhagic Telangiectasia Presenting as High Output Cardiac Failure during Pregnancy.

Authors:  Tareq Goussous; Alex Haynes; Katherine Najarian; Marcos Daccarett; Shukri David
Journal:  Cardiol Res Pract       Date:  2009-09-07       Impact factor: 1.866

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