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Macrophage activation syndrome in MDA5 antibody-positive dermatomyositis and COVID-19 infection
BACKGROUND: Macrophage activation syndrome (MAS) is a rare multiorgan system disorder that may present as a fatal complication of underlying rheumatological disease, including dermatomyositis. CASE PRESENTATION: Here, we report the case of a 65-year-old Caucasian female with a history of psoriasis a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8666190/ https://www.ncbi.nlm.nih.gov/pubmed/34895325 http://dx.doi.org/10.1186/s41927-021-00225-z |
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author | Keshtkarjahromi, Marzieh Chhetri, Sumit Balagani, Amulya Tayyab, Umm-ul-Banin B. Haas, Christopher J. |
author_facet | Keshtkarjahromi, Marzieh Chhetri, Sumit Balagani, Amulya Tayyab, Umm-ul-Banin B. Haas, Christopher J. |
author_sort | Keshtkarjahromi, Marzieh |
collection | PubMed |
description | BACKGROUND: Macrophage activation syndrome (MAS) is a rare multiorgan system disorder that may present as a fatal complication of underlying rheumatological disease, including dermatomyositis. CASE PRESENTATION: Here, we report the case of a 65-year-old Caucasian female with a history of psoriasis and a recent diagnosis of Coronavirus disease 2019 (COVID-19) who presented with progressive generalized weakness, joint pains, an erythematous rash, shortness of breath, and weight loss. She was ultimately diagnosed with biopsy-confirmed melanoma differentiation-associated protein 5 (MDA5)-positive dermatomyositis complicated by MAS, requiring intravenous immunoglobulin and high-dose methylprednisolone. CONCLUSIONS: This report serves as a clinical reminder of the rare, yet clinically relevant association between MDA5-positive dermatomyositis and MAS, as well as highlights the potential contribution of other immune system activating diseases, such as COVID-19, associated with a cytokine storm and hyperinflammatory state. |
format | Online Article Text |
id | pubmed-8666190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-86661902021-12-13 Macrophage activation syndrome in MDA5 antibody-positive dermatomyositis and COVID-19 infection Keshtkarjahromi, Marzieh Chhetri, Sumit Balagani, Amulya Tayyab, Umm-ul-Banin B. Haas, Christopher J. BMC Rheumatol Case Report BACKGROUND: Macrophage activation syndrome (MAS) is a rare multiorgan system disorder that may present as a fatal complication of underlying rheumatological disease, including dermatomyositis. CASE PRESENTATION: Here, we report the case of a 65-year-old Caucasian female with a history of psoriasis and a recent diagnosis of Coronavirus disease 2019 (COVID-19) who presented with progressive generalized weakness, joint pains, an erythematous rash, shortness of breath, and weight loss. She was ultimately diagnosed with biopsy-confirmed melanoma differentiation-associated protein 5 (MDA5)-positive dermatomyositis complicated by MAS, requiring intravenous immunoglobulin and high-dose methylprednisolone. CONCLUSIONS: This report serves as a clinical reminder of the rare, yet clinically relevant association between MDA5-positive dermatomyositis and MAS, as well as highlights the potential contribution of other immune system activating diseases, such as COVID-19, associated with a cytokine storm and hyperinflammatory state. BioMed Central 2021-12-13 /pmc/articles/PMC8666190/ /pubmed/34895325 http://dx.doi.org/10.1186/s41927-021-00225-z Text en © The Author(s) 2021 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 | Case Report Keshtkarjahromi, Marzieh Chhetri, Sumit Balagani, Amulya Tayyab, Umm-ul-Banin B. Haas, Christopher J. Macrophage activation syndrome in MDA5 antibody-positive dermatomyositis and COVID-19 infection |
title | Macrophage activation syndrome in MDA5 antibody-positive dermatomyositis and COVID-19 infection |
title_full | Macrophage activation syndrome in MDA5 antibody-positive dermatomyositis and COVID-19 infection |
title_fullStr | Macrophage activation syndrome in MDA5 antibody-positive dermatomyositis and COVID-19 infection |
title_full_unstemmed | Macrophage activation syndrome in MDA5 antibody-positive dermatomyositis and COVID-19 infection |
title_short | Macrophage activation syndrome in MDA5 antibody-positive dermatomyositis and COVID-19 infection |
title_sort | macrophage activation syndrome in mda5 antibody-positive dermatomyositis and covid-19 infection |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8666190/ https://www.ncbi.nlm.nih.gov/pubmed/34895325 http://dx.doi.org/10.1186/s41927-021-00225-z |
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