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Hepatic Encephalopathy Is Not Always due to Liver Cirrhosis
Hepatic encephalopathy (HE) is a frequent and debilitating complication of liver disease and is oftentimes associated with hyperammonaemia. However, hyperammonaemia may occur in underlying conditions other than acute or chronic liver failure and clinical awareness is needed in order to be recognized...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9209981/ https://www.ncbi.nlm.nih.gov/pubmed/35814799 http://dx.doi.org/10.1159/000524551 |
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author | Ecker, Miriam Eva Paparoupa, Maria Sostmann, Bernd Weissenborn, Karin Schuppert, Frank |
author_facet | Ecker, Miriam Eva Paparoupa, Maria Sostmann, Bernd Weissenborn, Karin Schuppert, Frank |
author_sort | Ecker, Miriam Eva |
collection | PubMed |
description | Hepatic encephalopathy (HE) is a frequent and debilitating complication of liver disease and is oftentimes associated with hyperammonaemia. However, hyperammonaemia may occur in underlying conditions other than acute or chronic liver failure and clinical awareness is needed in order to be recognized and treated properly. A 24-year-old woman presented herself to our emergency department with acute confusion and altered mental state due to severe hyperammonaemia. The patient was diagnosed in the age of 14 with ornithine transcarbamylase (OTC) deficiency and was incompliant regarding her diet and suggested medication to treat this disorder. She was treated with sodium benzoate 250 mg/kg i.v., sodium phenylbutyrate/sodium phenylacetate 250 mg/kg i.v., L-arginine 250 mg/kg i.v., and received continuous hemofiltration. Under simultaneous medical treatment and haemodialysis, ammonia levels dropped to normal within 24 h and symptomatic encephalopathy ceased completely. OTC deficiency is rare in adults, and the majority of patients are diagnosed in childhood. It can lead to death if not diagnosed and treated properly. Our case underlines the importance of considering causes of HE other than liver cirrhosis. |
format | Online Article Text |
id | pubmed-9209981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-92099812022-07-08 Hepatic Encephalopathy Is Not Always due to Liver Cirrhosis Ecker, Miriam Eva Paparoupa, Maria Sostmann, Bernd Weissenborn, Karin Schuppert, Frank Case Rep Gastroenterol Single Case Hepatic encephalopathy (HE) is a frequent and debilitating complication of liver disease and is oftentimes associated with hyperammonaemia. However, hyperammonaemia may occur in underlying conditions other than acute or chronic liver failure and clinical awareness is needed in order to be recognized and treated properly. A 24-year-old woman presented herself to our emergency department with acute confusion and altered mental state due to severe hyperammonaemia. The patient was diagnosed in the age of 14 with ornithine transcarbamylase (OTC) deficiency and was incompliant regarding her diet and suggested medication to treat this disorder. She was treated with sodium benzoate 250 mg/kg i.v., sodium phenylbutyrate/sodium phenylacetate 250 mg/kg i.v., L-arginine 250 mg/kg i.v., and received continuous hemofiltration. Under simultaneous medical treatment and haemodialysis, ammonia levels dropped to normal within 24 h and symptomatic encephalopathy ceased completely. OTC deficiency is rare in adults, and the majority of patients are diagnosed in childhood. It can lead to death if not diagnosed and treated properly. Our case underlines the importance of considering causes of HE other than liver cirrhosis. S. Karger AG 2022-05-20 /pmc/articles/PMC9209981/ /pubmed/35814799 http://dx.doi.org/10.1159/000524551 Text en Copyright © 2022 by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission. |
spellingShingle | Single Case Ecker, Miriam Eva Paparoupa, Maria Sostmann, Bernd Weissenborn, Karin Schuppert, Frank Hepatic Encephalopathy Is Not Always due to Liver Cirrhosis |
title | Hepatic Encephalopathy Is Not Always due to Liver Cirrhosis |
title_full | Hepatic Encephalopathy Is Not Always due to Liver Cirrhosis |
title_fullStr | Hepatic Encephalopathy Is Not Always due to Liver Cirrhosis |
title_full_unstemmed | Hepatic Encephalopathy Is Not Always due to Liver Cirrhosis |
title_short | Hepatic Encephalopathy Is Not Always due to Liver Cirrhosis |
title_sort | hepatic encephalopathy is not always due to liver cirrhosis |
topic | Single Case |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9209981/ https://www.ncbi.nlm.nih.gov/pubmed/35814799 http://dx.doi.org/10.1159/000524551 |
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