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Severe Acute Liver Injury due to Secondary Hemophagocytic Lymphohistiocytosis: A Case Report
Severe acute liver injury (ALI) is mostly triggered by viral infections and hepatotoxic drugs; however, it can also be seen in systemic diseases. Hemophagocytic lymphohistiocytosis (HLH) is a rare, immune-mediated syndrome that presents as a life-threatening inflammatory disorder affecting multiple...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10661704/ https://www.ncbi.nlm.nih.gov/pubmed/38020822 http://dx.doi.org/10.1159/000529549 |
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author | Sequeira, Cristiana Lopes, Sara Ramos Neves, Anabela Santos, Inês Costa Martins, Cláudio Rodrigues Oliveira, Ana Paula |
author_facet | Sequeira, Cristiana Lopes, Sara Ramos Neves, Anabela Santos, Inês Costa Martins, Cláudio Rodrigues Oliveira, Ana Paula |
author_sort | Sequeira, Cristiana |
collection | PubMed |
description | Severe acute liver injury (ALI) is mostly triggered by viral infections and hepatotoxic drugs; however, it can also be seen in systemic diseases. Hemophagocytic lymphohistiocytosis (HLH) is a rare, immune-mediated syndrome that presents as a life-threatening inflammatory disorder affecting multiple organs. Secondary causes occur mainly in the set of malignancy, infection, and autoimmune disease, and are seldom triggered by vaccination. Although liver involvement is common, presentation as severe ALI is rare. We describe a case of a 65-year-old male with history of low-risk chronic lymphocytic leukemia and rheumatoid arthritis treated with prednisolone who presented with persistent fever and jaundice 1 week after COVID-19 vaccination. The diagnosis was challenging given the predominant liver impairment, characterized by hyperbilirubinemia, transaminases over 1,000 U/L, and prolonged INR, which prompted an extensive investigation and exclusion of autoimmune, toxic, and viral causes of hepatitis. Laboratory workup revealed bicytopenia, hyperferritinemia, which together with organ failure and evidence of hemophagocytosis in bone marrow suggested the diagnosis of HLH. After excluding infectious etiologies, flare of rheumatological disease, and the progression of hematological disease, HLH was diagnosed. He was successfully treated with etoposide and corticosteroids, with dramatic improvement of liver tests. After exclusion of other causes of secondary HLH, the recent vaccination for COVID-19 was the likely trigger. We report a case of double rarity of HLH, as it presented with severe liver dysfunction which was probably triggered by vaccination. In this case, the predominant liver involvement urged extensive investigation of liver disease, so a high index of suspicion was required to make an early diagnosis. Clinicians should consider HLH in patients with unexplained signs and symptoms of systemic inflammatory response and multiorgan involvement, including severe liver involvement as the first presentation. |
format | Online Article Text |
id | pubmed-10661704 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-106617042023-03-30 Severe Acute Liver Injury due to Secondary Hemophagocytic Lymphohistiocytosis: A Case Report Sequeira, Cristiana Lopes, Sara Ramos Neves, Anabela Santos, Inês Costa Martins, Cláudio Rodrigues Oliveira, Ana Paula GE Port J Gastroenterol Clinical Case Study Severe acute liver injury (ALI) is mostly triggered by viral infections and hepatotoxic drugs; however, it can also be seen in systemic diseases. Hemophagocytic lymphohistiocytosis (HLH) is a rare, immune-mediated syndrome that presents as a life-threatening inflammatory disorder affecting multiple organs. Secondary causes occur mainly in the set of malignancy, infection, and autoimmune disease, and are seldom triggered by vaccination. Although liver involvement is common, presentation as severe ALI is rare. We describe a case of a 65-year-old male with history of low-risk chronic lymphocytic leukemia and rheumatoid arthritis treated with prednisolone who presented with persistent fever and jaundice 1 week after COVID-19 vaccination. The diagnosis was challenging given the predominant liver impairment, characterized by hyperbilirubinemia, transaminases over 1,000 U/L, and prolonged INR, which prompted an extensive investigation and exclusion of autoimmune, toxic, and viral causes of hepatitis. Laboratory workup revealed bicytopenia, hyperferritinemia, which together with organ failure and evidence of hemophagocytosis in bone marrow suggested the diagnosis of HLH. After excluding infectious etiologies, flare of rheumatological disease, and the progression of hematological disease, HLH was diagnosed. He was successfully treated with etoposide and corticosteroids, with dramatic improvement of liver tests. After exclusion of other causes of secondary HLH, the recent vaccination for COVID-19 was the likely trigger. We report a case of double rarity of HLH, as it presented with severe liver dysfunction which was probably triggered by vaccination. In this case, the predominant liver involvement urged extensive investigation of liver disease, so a high index of suspicion was required to make an early diagnosis. Clinicians should consider HLH in patients with unexplained signs and symptoms of systemic inflammatory response and multiorgan involvement, including severe liver involvement as the first presentation. S. Karger AG 2023-03-30 /pmc/articles/PMC10661704/ /pubmed/38020822 http://dx.doi.org/10.1159/000529549 Text en Copyright © 2023 by The Author(s). Published 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). Usage and distribution for commercial purposes requires written permission. |
spellingShingle | Clinical Case Study Sequeira, Cristiana Lopes, Sara Ramos Neves, Anabela Santos, Inês Costa Martins, Cláudio Rodrigues Oliveira, Ana Paula Severe Acute Liver Injury due to Secondary Hemophagocytic Lymphohistiocytosis: A Case Report |
title | Severe Acute Liver Injury due to Secondary Hemophagocytic Lymphohistiocytosis: A Case Report |
title_full | Severe Acute Liver Injury due to Secondary Hemophagocytic Lymphohistiocytosis: A Case Report |
title_fullStr | Severe Acute Liver Injury due to Secondary Hemophagocytic Lymphohistiocytosis: A Case Report |
title_full_unstemmed | Severe Acute Liver Injury due to Secondary Hemophagocytic Lymphohistiocytosis: A Case Report |
title_short | Severe Acute Liver Injury due to Secondary Hemophagocytic Lymphohistiocytosis: A Case Report |
title_sort | severe acute liver injury due to secondary hemophagocytic lymphohistiocytosis: a case report |
topic | Clinical Case Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10661704/ https://www.ncbi.nlm.nih.gov/pubmed/38020822 http://dx.doi.org/10.1159/000529549 |
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