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A Rare Case of Henoch-Schönlein Purpura Following a COVID-19 Vaccine—Case Report

In the COVID-19 pandemic era, anti-SARS-CoV-2 vaccination is considered to be the most efficient way to overtake the COVID-19 scourge. Like all medicines, vaccines are not devoid of risks and can in rare cases cause some various side effects. The objective of this case report is to highlight this un...

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Autores principales: Naitlho, Abdelhamid, Lahlou, Wahib, Bourial, Abderrahim, Rais, Hamza, Ismaili, Nabil, Abousahfa, Imad, Belyamani, Lahcen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8425851/
https://www.ncbi.nlm.nih.gov/pubmed/34518812
http://dx.doi.org/10.1007/s42399-021-01025-9
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author Naitlho, Abdelhamid
Lahlou, Wahib
Bourial, Abderrahim
Rais, Hamza
Ismaili, Nabil
Abousahfa, Imad
Belyamani, Lahcen
author_facet Naitlho, Abdelhamid
Lahlou, Wahib
Bourial, Abderrahim
Rais, Hamza
Ismaili, Nabil
Abousahfa, Imad
Belyamani, Lahcen
author_sort Naitlho, Abdelhamid
collection PubMed
description In the COVID-19 pandemic era, anti-SARS-CoV-2 vaccination is considered to be the most efficient way to overtake the COVID-19 scourge. Like all medicines, vaccines are not devoid of risks and can in rare cases cause some various side effects. The objective of this case report is to highlight this unusual presentation of Henoch-Schönlein purpura following an anti-COVID-19 vaccination in a 62-year-old adult. The 62-year-old patient admitted to the emergency room for a petechial purpuric rash, sloping, occurring within hours, involving both legs and ascending. The clinical signs also included polyarthralgia and hematuria. Reported in the history the notion of an anti-COVID-19 vaccination 8 days prior to the onset of symptomatology. In the case of our patient, we retain the diagnosis of rheumatoid purpura based on the EULAR/PRINTO/PReS diagnostic criteria. Corticosteroid therapy (prednisone) was started, resulting to a rapid regression of clinical and laboratory symptoms, few days after the treatment. Patient was asymptomatic on subsequent visits. The low number of published cases of post-vaccine vasculitis does not question the safety of vaccines, but knowledge of such complications deserves to be known in order to avoid new immunizations that could have more serious consequences, and to avoid aggravating or reactivating a pre-existing vasculitis.
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spelling pubmed-84258512021-09-09 A Rare Case of Henoch-Schönlein Purpura Following a COVID-19 Vaccine—Case Report Naitlho, Abdelhamid Lahlou, Wahib Bourial, Abderrahim Rais, Hamza Ismaili, Nabil Abousahfa, Imad Belyamani, Lahcen SN Compr Clin Med Case Report In the COVID-19 pandemic era, anti-SARS-CoV-2 vaccination is considered to be the most efficient way to overtake the COVID-19 scourge. Like all medicines, vaccines are not devoid of risks and can in rare cases cause some various side effects. The objective of this case report is to highlight this unusual presentation of Henoch-Schönlein purpura following an anti-COVID-19 vaccination in a 62-year-old adult. The 62-year-old patient admitted to the emergency room for a petechial purpuric rash, sloping, occurring within hours, involving both legs and ascending. The clinical signs also included polyarthralgia and hematuria. Reported in the history the notion of an anti-COVID-19 vaccination 8 days prior to the onset of symptomatology. In the case of our patient, we retain the diagnosis of rheumatoid purpura based on the EULAR/PRINTO/PReS diagnostic criteria. Corticosteroid therapy (prednisone) was started, resulting to a rapid regression of clinical and laboratory symptoms, few days after the treatment. Patient was asymptomatic on subsequent visits. The low number of published cases of post-vaccine vasculitis does not question the safety of vaccines, but knowledge of such complications deserves to be known in order to avoid new immunizations that could have more serious consequences, and to avoid aggravating or reactivating a pre-existing vasculitis. Springer International Publishing 2021-09-08 2021 /pmc/articles/PMC8425851/ /pubmed/34518812 http://dx.doi.org/10.1007/s42399-021-01025-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Case Report
Naitlho, Abdelhamid
Lahlou, Wahib
Bourial, Abderrahim
Rais, Hamza
Ismaili, Nabil
Abousahfa, Imad
Belyamani, Lahcen
A Rare Case of Henoch-Schönlein Purpura Following a COVID-19 Vaccine—Case Report
title A Rare Case of Henoch-Schönlein Purpura Following a COVID-19 Vaccine—Case Report
title_full A Rare Case of Henoch-Schönlein Purpura Following a COVID-19 Vaccine—Case Report
title_fullStr A Rare Case of Henoch-Schönlein Purpura Following a COVID-19 Vaccine—Case Report
title_full_unstemmed A Rare Case of Henoch-Schönlein Purpura Following a COVID-19 Vaccine—Case Report
title_short A Rare Case of Henoch-Schönlein Purpura Following a COVID-19 Vaccine—Case Report
title_sort rare case of henoch-schönlein purpura following a covid-19 vaccine—case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8425851/
https://www.ncbi.nlm.nih.gov/pubmed/34518812
http://dx.doi.org/10.1007/s42399-021-01025-9
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