Literature DB >> 27864871

Hereditary haemorrhagic telangiectasia: to transplant or not to transplant?

Carlo Sabbà1.   

Abstract

The Association of hereditary hemorrhagic telangiectasia (HHT) and type I hereditary angioedema is a very rare condition in medicine. The case reported by Muller et al., describes the coexistence of the two diseases and emphasizes the need for listing HHT patients for liver transplantation in case indications occurs, such as the presence of HCC, abnormally increased cardiac output, and gastrointestinal bleeding as reported for this case. The case described by Mueller et al. is anecdotal for the usefulness of liver transplantation in HHT patients and shows that liver transplantation may be the best supportive care and, sometimes, the unique and final therapeutic option for these patients.
© 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  hereditary haemorrhagic telangiectasia; liver transplantation; type I hereditary angioedema

Mesh:

Year:  2016        PMID: 27864871     DOI: 10.1111/liv.13247

Source DB:  PubMed          Journal:  Liver Int        ISSN: 1478-3223            Impact factor:   5.828


  1 in total

1.  Liver cirrhosis in a patient with hepatic hereditary hemorrhagic telangiectasia and Budd-Chiari syndrome: a case report.

Authors:  Bai-Guo Xu; Jing Liang; Ke-Feng Jia; Tao Han
Journal:  BMC Gastroenterol       Date:  2020-06-03       Impact factor: 3.067

  1 in total

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