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Atypical adult-onset Still’s disease with an initial and sole manifestation of liver injury: A case report and review of literature
BACKGROUND: Adult-onset Still's disease (AOSD) typically presents with a high spiking fever, polyarthritis, transient maculopapular rash, neutrophilic leukocytosis, and hepatosplenomegaly. It has a wide spectrum of clinical symptoms ranging from mild to severe, with extensive involvement of alm...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809657/ https://www.ncbi.nlm.nih.gov/pubmed/33511189 http://dx.doi.org/10.12998/wjcc.v9.i1.224 |
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author | Yu, Fan Qin, Shao-You Zhou, Chang-Yu Zhao, Lu Xu, Yan Jia, Er-Na Wang, Jiang-Bin |
author_facet | Yu, Fan Qin, Shao-You Zhou, Chang-Yu Zhao, Lu Xu, Yan Jia, Er-Na Wang, Jiang-Bin |
author_sort | Yu, Fan |
collection | PubMed |
description | BACKGROUND: Adult-onset Still's disease (AOSD) typically presents with a high spiking fever, polyarthritis, transient maculopapular rash, neutrophilic leukocytosis, and hepatosplenomegaly. It has a wide spectrum of clinical symptoms ranging from mild to severe, with extensive involvement of almost every organ. Although liver involvement in the form of increased hepatic enzymes and bilirubin is common, no AOSD case with liver involvement as the initial manifestation of AOSD has been reported. CASE SUMMARY: A 35-year-old woman presented to the hepatology department with progressively worsening jaundice for one week. Liver chemistry tests revealed a significantly increased liver enzymes and bilirubin level. Given that the clinical examination was unremarkable, liver biopsy was considered because the patient had a history of AOSD 6 years ago. Liver histopathology revealed that most hepatic lobules were still recognizable. Fusional necrosis was observed around most central veins. A few bridging necrotic zones were also found. Infiltration of multiple plasma cells were observed in the necrotic zone, and the reticular scaffold was still expanded. Additionally, no obvious fibrosis was observed in the portal area. Mild mixed inflammatory cell infiltration was noted in the interstitium of the portal area. Further examination was unremarkable except for a remarkably high level of ferritin. Collectively, a presumptive diagnosis of liver injury secondary to AOSD was made. The hepatic involvement responded well to glucocorticoid treatment. CONCLUSION: This case highlights that hepatic involvement as an initial and sole manifestation could be a pattern of relapsed AOSD. The diagnosis of AOSD should be considered in the case of nonresolving liver injury after the exclusion of common etiologies for liver diseases. A liver biopsy can be useful for the differential diagnosis of liver injury associated with AOSD. |
format | Online Article Text |
id | pubmed-7809657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-78096572021-01-27 Atypical adult-onset Still’s disease with an initial and sole manifestation of liver injury: A case report and review of literature Yu, Fan Qin, Shao-You Zhou, Chang-Yu Zhao, Lu Xu, Yan Jia, Er-Na Wang, Jiang-Bin World J Clin Cases Case Report BACKGROUND: Adult-onset Still's disease (AOSD) typically presents with a high spiking fever, polyarthritis, transient maculopapular rash, neutrophilic leukocytosis, and hepatosplenomegaly. It has a wide spectrum of clinical symptoms ranging from mild to severe, with extensive involvement of almost every organ. Although liver involvement in the form of increased hepatic enzymes and bilirubin is common, no AOSD case with liver involvement as the initial manifestation of AOSD has been reported. CASE SUMMARY: A 35-year-old woman presented to the hepatology department with progressively worsening jaundice for one week. Liver chemistry tests revealed a significantly increased liver enzymes and bilirubin level. Given that the clinical examination was unremarkable, liver biopsy was considered because the patient had a history of AOSD 6 years ago. Liver histopathology revealed that most hepatic lobules were still recognizable. Fusional necrosis was observed around most central veins. A few bridging necrotic zones were also found. Infiltration of multiple plasma cells were observed in the necrotic zone, and the reticular scaffold was still expanded. Additionally, no obvious fibrosis was observed in the portal area. Mild mixed inflammatory cell infiltration was noted in the interstitium of the portal area. Further examination was unremarkable except for a remarkably high level of ferritin. Collectively, a presumptive diagnosis of liver injury secondary to AOSD was made. The hepatic involvement responded well to glucocorticoid treatment. CONCLUSION: This case highlights that hepatic involvement as an initial and sole manifestation could be a pattern of relapsed AOSD. The diagnosis of AOSD should be considered in the case of nonresolving liver injury after the exclusion of common etiologies for liver diseases. A liver biopsy can be useful for the differential diagnosis of liver injury associated with AOSD. Baishideng Publishing Group Inc 2021-01-06 2021-01-06 /pmc/articles/PMC7809657/ /pubmed/33511189 http://dx.doi.org/10.12998/wjcc.v9.i1.224 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Case Report Yu, Fan Qin, Shao-You Zhou, Chang-Yu Zhao, Lu Xu, Yan Jia, Er-Na Wang, Jiang-Bin Atypical adult-onset Still’s disease with an initial and sole manifestation of liver injury: A case report and review of literature |
title | Atypical adult-onset Still’s disease with an initial and sole manifestation of liver injury: A case report and review of literature |
title_full | Atypical adult-onset Still’s disease with an initial and sole manifestation of liver injury: A case report and review of literature |
title_fullStr | Atypical adult-onset Still’s disease with an initial and sole manifestation of liver injury: A case report and review of literature |
title_full_unstemmed | Atypical adult-onset Still’s disease with an initial and sole manifestation of liver injury: A case report and review of literature |
title_short | Atypical adult-onset Still’s disease with an initial and sole manifestation of liver injury: A case report and review of literature |
title_sort | atypical adult-onset still’s disease with an initial and sole manifestation of liver injury: a case report and review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809657/ https://www.ncbi.nlm.nih.gov/pubmed/33511189 http://dx.doi.org/10.12998/wjcc.v9.i1.224 |
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