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Adult-onset Still's disease evolving with multiple organ failure and death: A case report and review of the literature

BACKGROUND: Adult-onset Still’s disease (AOSD) is a rare systemic inflammatory disease, which is characterized by daily fever and arthritis, with an evanescent rash and neutrophilic leukocytosis. To date, there has been no definite laboratory or imaging test available for diagnosing AOSD; the diagno...

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Autores principales: Han, Zhong-Bin, Wu, Ju, Liu, Jing, Li, He-Ming, Guo, Kai, Sun, Tong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852636/
https://www.ncbi.nlm.nih.gov/pubmed/33585636
http://dx.doi.org/10.12998/wjcc.v9.i4.886
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author Han, Zhong-Bin
Wu, Ju
Liu, Jing
Li, He-Ming
Guo, Kai
Sun, Tong
author_facet Han, Zhong-Bin
Wu, Ju
Liu, Jing
Li, He-Ming
Guo, Kai
Sun, Tong
author_sort Han, Zhong-Bin
collection PubMed
description BACKGROUND: Adult-onset Still’s disease (AOSD) is a rare systemic inflammatory disease, which is characterized by daily fever and arthritis, with an evanescent rash and neutrophilic leukocytosis. To date, there has been no definite laboratory or imaging test available for diagnosing AOSD; the diagnosis is one of exclusion, which can be very challenging. In particular, AOSD patients may experience different complications affecting their clinical picture, management, and prognosis. The treatment of AOSD remains largely empirical and involves therapeutic agents. CASE SUMMARY: We report the case of a 36-year-old woman who presented with fever, red rash, arthralgia, and sore throat. Her serum ferritin level and white blood cell count were markedly elevated, and the first diagnosis 22 years prior was "juvenile rheumatoid arthritis of systemic type". The patient was treated with prednisone, sulfasalazine, methotrexate, and leflunomide. After remission of her symptoms, the patient stopped taking the medications, and the disease recurred. Ultimately, the patient was diagnosed with adult-onset Still's disease. Relapse occurred several times due to self-medication withdrawal, and an interleukin-6 antagonist (tocilizumab/Actemra) was administered to control the disease. Recently, she was hospitalized because an incision did not heal, and the patient suddenly developed high fever and diarrhea during hospitalization. The patient's disease progressed violently and quickly developed into macrophage activation syndrome, disseminated intravascular coagulation, shock, and multiple organ failure. The patient had sudden cardiac arrest, and she died despite emergency rescue efforts. CONCLUSION: AOSD patients need regular follow-up in the long-term treatment process, and must press formulary standard medication, and do not voluntarily withdraw or reduce the dose. Otherwise it may cause disease back-and-forth or serious life-threatening complications. Meanwhile, strict management of trauma, infections, tumors, and other diseases may contribute to improved outcomes in patients with complications.
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spelling pubmed-78526362021-02-12 Adult-onset Still's disease evolving with multiple organ failure and death: A case report and review of the literature Han, Zhong-Bin Wu, Ju Liu, Jing Li, He-Ming Guo, Kai Sun, Tong World J Clin Cases Case Report BACKGROUND: Adult-onset Still’s disease (AOSD) is a rare systemic inflammatory disease, which is characterized by daily fever and arthritis, with an evanescent rash and neutrophilic leukocytosis. To date, there has been no definite laboratory or imaging test available for diagnosing AOSD; the diagnosis is one of exclusion, which can be very challenging. In particular, AOSD patients may experience different complications affecting their clinical picture, management, and prognosis. The treatment of AOSD remains largely empirical and involves therapeutic agents. CASE SUMMARY: We report the case of a 36-year-old woman who presented with fever, red rash, arthralgia, and sore throat. Her serum ferritin level and white blood cell count were markedly elevated, and the first diagnosis 22 years prior was "juvenile rheumatoid arthritis of systemic type". The patient was treated with prednisone, sulfasalazine, methotrexate, and leflunomide. After remission of her symptoms, the patient stopped taking the medications, and the disease recurred. Ultimately, the patient was diagnosed with adult-onset Still's disease. Relapse occurred several times due to self-medication withdrawal, and an interleukin-6 antagonist (tocilizumab/Actemra) was administered to control the disease. Recently, she was hospitalized because an incision did not heal, and the patient suddenly developed high fever and diarrhea during hospitalization. The patient's disease progressed violently and quickly developed into macrophage activation syndrome, disseminated intravascular coagulation, shock, and multiple organ failure. The patient had sudden cardiac arrest, and she died despite emergency rescue efforts. CONCLUSION: AOSD patients need regular follow-up in the long-term treatment process, and must press formulary standard medication, and do not voluntarily withdraw or reduce the dose. Otherwise it may cause disease back-and-forth or serious life-threatening complications. Meanwhile, strict management of trauma, infections, tumors, and other diseases may contribute to improved outcomes in patients with complications. Baishideng Publishing Group Inc 2021-02-06 2021-02-06 /pmc/articles/PMC7852636/ /pubmed/33585636 http://dx.doi.org/10.12998/wjcc.v9.i4.886 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
Han, Zhong-Bin
Wu, Ju
Liu, Jing
Li, He-Ming
Guo, Kai
Sun, Tong
Adult-onset Still's disease evolving with multiple organ failure and death: A case report and review of the literature
title Adult-onset Still's disease evolving with multiple organ failure and death: A case report and review of the literature
title_full Adult-onset Still's disease evolving with multiple organ failure and death: A case report and review of the literature
title_fullStr Adult-onset Still's disease evolving with multiple organ failure and death: A case report and review of the literature
title_full_unstemmed Adult-onset Still's disease evolving with multiple organ failure and death: A case report and review of the literature
title_short Adult-onset Still's disease evolving with multiple organ failure and death: A case report and review of the literature
title_sort adult-onset still's disease evolving with multiple organ failure and death: a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852636/
https://www.ncbi.nlm.nih.gov/pubmed/33585636
http://dx.doi.org/10.12998/wjcc.v9.i4.886
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