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Clinicopathologic features of de novo non-alcoholic steatohepatitis in the post-transplant setting
BACKGROUND: Non-alcoholic steatohepatitis (NASH) has become an increasingly recognized problem in patients after orthotopic liver transplant. The aims of this study were to compare the clinicopathologic features of recurrent and de novo NASH. METHODS: From 1995 to 2016, we performed a retrospective...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9367095/ https://www.ncbi.nlm.nih.gov/pubmed/35948927 http://dx.doi.org/10.1186/s13000-022-01247-y |
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author | Balitzer, Dana Tsai, Jia-Huei Gill, Ryan M. |
author_facet | Balitzer, Dana Tsai, Jia-Huei Gill, Ryan M. |
author_sort | Balitzer, Dana |
collection | PubMed |
description | BACKGROUND: Non-alcoholic steatohepatitis (NASH) has become an increasingly recognized problem in patients after orthotopic liver transplant. The aims of this study were to compare the clinicopathologic features of recurrent and de novo NASH. METHODS: From 1995 to 2016, we performed a retrospective review of patients with a histological diagnosis of non-alcoholic steatohepatitis made more than 6 months after liver transplant at University of California, San Francisco. The cases were categorized into de novo (n = 19) or recurrent steatohepatitis (n = 37). RESULTS: Hepatitis C virus (HCV) infection-related cirrhosis was the most common etiology of transplantation in de novo NASH (78% of cases, n = 29). There was no difference in glycogenosis or presence of grade 3 steatosis. More recurrent NASH biopsies had small ballooned hepatocytes (62.5% of cases) compared to de novo NASH (26.7%) (p = 0.03), and were less likely to show prominent portal inflammation (5% versus 40.5%, p = 0.0049). The diagnosis of recurrent NASH was made significantly sooner after transplantation than the diagnosis of de novo NASH (2.8 years versus 4.8 years, p = 0.02). CONCLUSIONS: Overall, our results support that recurrent NASH demonstrates distinct clinicopathologic features compared to de novo NASH arising in the post-transplant setting. |
format | Online Article Text |
id | pubmed-9367095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-93670952022-08-12 Clinicopathologic features of de novo non-alcoholic steatohepatitis in the post-transplant setting Balitzer, Dana Tsai, Jia-Huei Gill, Ryan M. Diagn Pathol Research BACKGROUND: Non-alcoholic steatohepatitis (NASH) has become an increasingly recognized problem in patients after orthotopic liver transplant. The aims of this study were to compare the clinicopathologic features of recurrent and de novo NASH. METHODS: From 1995 to 2016, we performed a retrospective review of patients with a histological diagnosis of non-alcoholic steatohepatitis made more than 6 months after liver transplant at University of California, San Francisco. The cases were categorized into de novo (n = 19) or recurrent steatohepatitis (n = 37). RESULTS: Hepatitis C virus (HCV) infection-related cirrhosis was the most common etiology of transplantation in de novo NASH (78% of cases, n = 29). There was no difference in glycogenosis or presence of grade 3 steatosis. More recurrent NASH biopsies had small ballooned hepatocytes (62.5% of cases) compared to de novo NASH (26.7%) (p = 0.03), and were less likely to show prominent portal inflammation (5% versus 40.5%, p = 0.0049). The diagnosis of recurrent NASH was made significantly sooner after transplantation than the diagnosis of de novo NASH (2.8 years versus 4.8 years, p = 0.02). CONCLUSIONS: Overall, our results support that recurrent NASH demonstrates distinct clinicopathologic features compared to de novo NASH arising in the post-transplant setting. BioMed Central 2022-08-10 /pmc/articles/PMC9367095/ /pubmed/35948927 http://dx.doi.org/10.1186/s13000-022-01247-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Balitzer, Dana Tsai, Jia-Huei Gill, Ryan M. Clinicopathologic features of de novo non-alcoholic steatohepatitis in the post-transplant setting |
title | Clinicopathologic features of de novo non-alcoholic steatohepatitis in the post-transplant setting |
title_full | Clinicopathologic features of de novo non-alcoholic steatohepatitis in the post-transplant setting |
title_fullStr | Clinicopathologic features of de novo non-alcoholic steatohepatitis in the post-transplant setting |
title_full_unstemmed | Clinicopathologic features of de novo non-alcoholic steatohepatitis in the post-transplant setting |
title_short | Clinicopathologic features of de novo non-alcoholic steatohepatitis in the post-transplant setting |
title_sort | clinicopathologic features of de novo non-alcoholic steatohepatitis in the post-transplant setting |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9367095/ https://www.ncbi.nlm.nih.gov/pubmed/35948927 http://dx.doi.org/10.1186/s13000-022-01247-y |
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