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Cutaneous polyarteritis nodosa in a 7-year-old boy: difficulties in diagnosis

Vasculitides are a diverse group of diseases. The potential diversity of their clinical symptoms requires the exclusion of other systemic connective tissue diseases, infectious diseases or malignancies. Due to similar clinical manifestations, comprehensive differential diagnosis is needed. This pape...

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Detalles Bibliográficos
Autores principales: Dybowska-Gołota, Izabela, Krajewska-Włodarczyk, Magdalena, Żuber, Zbigniew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6911246/
https://www.ncbi.nlm.nih.gov/pubmed/31844345
http://dx.doi.org/10.5114/reum.2019.89525
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author Dybowska-Gołota, Izabela
Krajewska-Włodarczyk, Magdalena
Żuber, Zbigniew
author_facet Dybowska-Gołota, Izabela
Krajewska-Włodarczyk, Magdalena
Żuber, Zbigniew
author_sort Dybowska-Gołota, Izabela
collection PubMed
description Vasculitides are a diverse group of diseases. The potential diversity of their clinical symptoms requires the exclusion of other systemic connective tissue diseases, infectious diseases or malignancies. Due to similar clinical manifestations, comprehensive differential diagnosis is needed. This paper presents the case of a boy in whom polyarteritis nodosa, early stage of Behçet’s disease or autoimmune/autoinflammatory syndrome induced by adjuvants was suspected following initial diagnostics. He was ultimately diagnosed with cutaneous polyarteritis nodosa.
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spelling pubmed-69112462019-12-16 Cutaneous polyarteritis nodosa in a 7-year-old boy: difficulties in diagnosis Dybowska-Gołota, Izabela Krajewska-Włodarczyk, Magdalena Żuber, Zbigniew Reumatologia Case Report Vasculitides are a diverse group of diseases. The potential diversity of their clinical symptoms requires the exclusion of other systemic connective tissue diseases, infectious diseases or malignancies. Due to similar clinical manifestations, comprehensive differential diagnosis is needed. This paper presents the case of a boy in whom polyarteritis nodosa, early stage of Behçet’s disease or autoimmune/autoinflammatory syndrome induced by adjuvants was suspected following initial diagnostics. He was ultimately diagnosed with cutaneous polyarteritis nodosa. Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie 2019-10-31 2019 /pmc/articles/PMC6911246/ /pubmed/31844345 http://dx.doi.org/10.5114/reum.2019.89525 Text en Copyright: © 2019 Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Case Report
Dybowska-Gołota, Izabela
Krajewska-Włodarczyk, Magdalena
Żuber, Zbigniew
Cutaneous polyarteritis nodosa in a 7-year-old boy: difficulties in diagnosis
title Cutaneous polyarteritis nodosa in a 7-year-old boy: difficulties in diagnosis
title_full Cutaneous polyarteritis nodosa in a 7-year-old boy: difficulties in diagnosis
title_fullStr Cutaneous polyarteritis nodosa in a 7-year-old boy: difficulties in diagnosis
title_full_unstemmed Cutaneous polyarteritis nodosa in a 7-year-old boy: difficulties in diagnosis
title_short Cutaneous polyarteritis nodosa in a 7-year-old boy: difficulties in diagnosis
title_sort cutaneous polyarteritis nodosa in a 7-year-old boy: difficulties in diagnosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6911246/
https://www.ncbi.nlm.nih.gov/pubmed/31844345
http://dx.doi.org/10.5114/reum.2019.89525
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