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Adverse Reaction to COVID-19 mRNA Vaccination in a Patient With VEXAS Syndrome

VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome is a rare genetic disorder originating from a somatic mutation in the hematopoietic stem cells. This syndrome was first described in 2020 and carries many clinical features that other conditions cannot explain. Widespread auto...

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Detalles Bibliográficos
Autor principal: Ciprian, Giulio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034849/
https://www.ncbi.nlm.nih.gov/pubmed/35481304
http://dx.doi.org/10.7759/cureus.23456
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author Ciprian, Giulio
author_facet Ciprian, Giulio
author_sort Ciprian, Giulio
collection PubMed
description VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome is a rare genetic disorder originating from a somatic mutation in the hematopoietic stem cells. This syndrome was first described in 2020 and carries many clinical features that other conditions cannot explain. Widespread autoinflammation is the primary process the disease presents, with high morbidity and mortality in those who show signs of bone marrow failure. Treatment is complex, and response to current therapies is poor. Long-term prognosis carries a mortality of 50%. In addition, the advancement of new-generation messenger ribonucleic acid (mRNA) vaccines raises concerns about their safety in this population since it could trigger a vaccine-related autoimmune response. This case describes the hospital course of a male in his 50s exhibiting an unexplained cutaneous reaction to an mRNA COVID-19 vaccine. He was later diagnosed with VEXAS syndrome based on symptoms presentation and diagnostic workup.
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spelling pubmed-90348492022-04-26 Adverse Reaction to COVID-19 mRNA Vaccination in a Patient With VEXAS Syndrome Ciprian, Giulio Cureus Genetics VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome is a rare genetic disorder originating from a somatic mutation in the hematopoietic stem cells. This syndrome was first described in 2020 and carries many clinical features that other conditions cannot explain. Widespread autoinflammation is the primary process the disease presents, with high morbidity and mortality in those who show signs of bone marrow failure. Treatment is complex, and response to current therapies is poor. Long-term prognosis carries a mortality of 50%. In addition, the advancement of new-generation messenger ribonucleic acid (mRNA) vaccines raises concerns about their safety in this population since it could trigger a vaccine-related autoimmune response. This case describes the hospital course of a male in his 50s exhibiting an unexplained cutaneous reaction to an mRNA COVID-19 vaccine. He was later diagnosed with VEXAS syndrome based on symptoms presentation and diagnostic workup. Cureus 2022-03-24 /pmc/articles/PMC9034849/ /pubmed/35481304 http://dx.doi.org/10.7759/cureus.23456 Text en Copyright © 2022, Ciprian et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Genetics
Ciprian, Giulio
Adverse Reaction to COVID-19 mRNA Vaccination in a Patient With VEXAS Syndrome
title Adverse Reaction to COVID-19 mRNA Vaccination in a Patient With VEXAS Syndrome
title_full Adverse Reaction to COVID-19 mRNA Vaccination in a Patient With VEXAS Syndrome
title_fullStr Adverse Reaction to COVID-19 mRNA Vaccination in a Patient With VEXAS Syndrome
title_full_unstemmed Adverse Reaction to COVID-19 mRNA Vaccination in a Patient With VEXAS Syndrome
title_short Adverse Reaction to COVID-19 mRNA Vaccination in a Patient With VEXAS Syndrome
title_sort adverse reaction to covid-19 mrna vaccination in a patient with vexas syndrome
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034849/
https://www.ncbi.nlm.nih.gov/pubmed/35481304
http://dx.doi.org/10.7759/cureus.23456
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