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Hypereosinophilic vasculitis with Raynaud phenomenon presentation: a case report

BACKGROUND: Previous case series have reported idiopathic eosinophilic vasculitis as a potential manifestation of hypereosinophilic syndrome (HES). This condition is characterized by digital necrotizing, systemic vasculitis that affects varying-sized blood vessels. This report presents our experienc...

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Autores principales: Phuong, Duy Le Cao, The, Hoa Bui, Duy, Quan Vo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10584751/
https://www.ncbi.nlm.nih.gov/pubmed/37851184
http://dx.doi.org/10.1186/s43044-023-00418-6
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author Phuong, Duy Le Cao
The, Hoa Bui
Duy, Quan Vo
author_facet Phuong, Duy Le Cao
The, Hoa Bui
Duy, Quan Vo
author_sort Phuong, Duy Le Cao
collection PubMed
description BACKGROUND: Previous case series have reported idiopathic eosinophilic vasculitis as a potential manifestation of hypereosinophilic syndrome (HES). This condition is characterized by digital necrotizing, systemic vasculitis that affects varying-sized blood vessels. This report presents our experience in treating a patient with eosinophilic vasculitis. CASE PRESENTATION: We describe the case of a 23-year-old man who presented with idiopathic HES, which manifested as digital ulcers and peripheral ischemia in both the upper and lower limbs, without the involvement of other organ systems. After ruling out primary and secondary causes of eosinophilia, a diagnosis of HES was established. Our patient has shown a positive response to corticosteroid therapy. CONCLUSIONS: Our case contributes to the existing evidence about diagnosing idiopathic eosinophilic vasculitis in patients with HES. We observed a favorable response to corticosteroid treatment in our patient.
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spelling pubmed-105847512023-10-20 Hypereosinophilic vasculitis with Raynaud phenomenon presentation: a case report Phuong, Duy Le Cao The, Hoa Bui Duy, Quan Vo Egypt Heart J Case Report BACKGROUND: Previous case series have reported idiopathic eosinophilic vasculitis as a potential manifestation of hypereosinophilic syndrome (HES). This condition is characterized by digital necrotizing, systemic vasculitis that affects varying-sized blood vessels. This report presents our experience in treating a patient with eosinophilic vasculitis. CASE PRESENTATION: We describe the case of a 23-year-old man who presented with idiopathic HES, which manifested as digital ulcers and peripheral ischemia in both the upper and lower limbs, without the involvement of other organ systems. After ruling out primary and secondary causes of eosinophilia, a diagnosis of HES was established. Our patient has shown a positive response to corticosteroid therapy. CONCLUSIONS: Our case contributes to the existing evidence about diagnosing idiopathic eosinophilic vasculitis in patients with HES. We observed a favorable response to corticosteroid treatment in our patient. Springer Berlin Heidelberg 2023-10-18 /pmc/articles/PMC10584751/ /pubmed/37851184 http://dx.doi.org/10.1186/s43044-023-00418-6 Text en © The Author(s) 2023 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
Phuong, Duy Le Cao
The, Hoa Bui
Duy, Quan Vo
Hypereosinophilic vasculitis with Raynaud phenomenon presentation: a case report
title Hypereosinophilic vasculitis with Raynaud phenomenon presentation: a case report
title_full Hypereosinophilic vasculitis with Raynaud phenomenon presentation: a case report
title_fullStr Hypereosinophilic vasculitis with Raynaud phenomenon presentation: a case report
title_full_unstemmed Hypereosinophilic vasculitis with Raynaud phenomenon presentation: a case report
title_short Hypereosinophilic vasculitis with Raynaud phenomenon presentation: a case report
title_sort hypereosinophilic vasculitis with raynaud phenomenon presentation: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10584751/
https://www.ncbi.nlm.nih.gov/pubmed/37851184
http://dx.doi.org/10.1186/s43044-023-00418-6
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