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Peliosis hepatis associated with hereditary haemorrhagic telangiectasia
Hereditary haemorrhagic telangiectasia (HHT) is an autosomal, predominantly inherited disease characterized by diffuse telangiectases involving the skin, mucous membranes, lung, brain, gastrointestinal tract and liver. Peliosis hepatis is a rare, benign disorder causing sinusoidal dilatation and the...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3938001/ https://www.ncbi.nlm.nih.gov/pubmed/24759967 http://dx.doi.org/10.1093/gastro/got021 |
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author | Alessandrino, F. Felisaz, P.F. La Fianza, A. |
author_facet | Alessandrino, F. Felisaz, P.F. La Fianza, A. |
author_sort | Alessandrino, F. |
collection | PubMed |
description | Hereditary haemorrhagic telangiectasia (HHT) is an autosomal, predominantly inherited disease characterized by diffuse telangiectases involving the skin, mucous membranes, lung, brain, gastrointestinal tract and liver. Peliosis hepatis is a rare, benign disorder causing sinusoidal dilatation and the presence of multiple blood-filled lacunar spaces within the liver. We report a case of an HHT patient with incidental magnetic resonance findings of focal hepatic peliosis. |
format | Online Article Text |
id | pubmed-3938001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39380012014-03-04 Peliosis hepatis associated with hereditary haemorrhagic telangiectasia Alessandrino, F. Felisaz, P.F. La Fianza, A. Gastroenterol Rep (Oxf) Case Reports Hereditary haemorrhagic telangiectasia (HHT) is an autosomal, predominantly inherited disease characterized by diffuse telangiectases involving the skin, mucous membranes, lung, brain, gastrointestinal tract and liver. Peliosis hepatis is a rare, benign disorder causing sinusoidal dilatation and the presence of multiple blood-filled lacunar spaces within the liver. We report a case of an HHT patient with incidental magnetic resonance findings of focal hepatic peliosis. Oxford University Press 2013-11 2013-07-23 /pmc/articles/PMC3938001/ /pubmed/24759967 http://dx.doi.org/10.1093/gastro/got021 Text en © The Author(s) 2013. Published by Oxford University Press and the Digestive Science Publishing Co. Limited. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Alessandrino, F. Felisaz, P.F. La Fianza, A. Peliosis hepatis associated with hereditary haemorrhagic telangiectasia |
title | Peliosis hepatis associated with hereditary haemorrhagic telangiectasia |
title_full | Peliosis hepatis associated with hereditary haemorrhagic telangiectasia |
title_fullStr | Peliosis hepatis associated with hereditary haemorrhagic telangiectasia |
title_full_unstemmed | Peliosis hepatis associated with hereditary haemorrhagic telangiectasia |
title_short | Peliosis hepatis associated with hereditary haemorrhagic telangiectasia |
title_sort | peliosis hepatis associated with hereditary haemorrhagic telangiectasia |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3938001/ https://www.ncbi.nlm.nih.gov/pubmed/24759967 http://dx.doi.org/10.1093/gastro/got021 |
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