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Takayasu arteritis associated with autoimmune/inflammatory syndrome induced by adjuvants: a case-based review

Takayasu’s arteritis (TA) is a chronic granulomatous vasculitis that predominantly affects the aorta and its major branches. Despite advancements in the understanding of the pathogenic pathways of vascular inflammation, the etiology and predisposing factors of TA remain to be fully understood. In su...

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Autores principales: Simeonova, Desislava, Georgiev, Tsvetoslav, Shivacheva, Tanya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10015523/
https://www.ncbi.nlm.nih.gov/pubmed/36920514
http://dx.doi.org/10.1007/s00296-023-05309-2
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author Simeonova, Desislava
Georgiev, Tsvetoslav
Shivacheva, Tanya
author_facet Simeonova, Desislava
Georgiev, Tsvetoslav
Shivacheva, Tanya
author_sort Simeonova, Desislava
collection PubMed
description Takayasu’s arteritis (TA) is a chronic granulomatous vasculitis that predominantly affects the aorta and its major branches. Despite advancements in the understanding of the pathogenic pathways of vascular inflammation, the etiology and predisposing factors of TA remain to be fully understood. In susceptible individuals, exposure to adjuvants may trigger, unlock or unmask an autoimmune disorder, presenting as non-specific constitutional symptoms or a fully developed autoimmune syndrome such as vasculitis. Here, we hypothesize that TA could be triggered by siliconosis, a subtype of the autoimmune/inflammatory syndrome induced by adjuvants (ASIA). ASIA, also known as Shoenfeld syndrome, encompasses a wide range of autoimmune and immune-mediated diseases resulting from dysregulation of the immune response after exposure to agents with adjuvant activity. This case report describes the development of large artery vasculitis, TA, in an individual one year following the placement of silicone breast implants. The patient initially presented with non-specific symptoms, and multiple imaging methods were employed, including ultrasound diagnostics, CT angiography, and 18-fluorodeoxyglucose positron emission tomography/CT. These techniques revealed vasculitic alterations in the carotid arteries and thoracic aorta. Initial treatment with glucocorticosteroids proved ineffective, prompting the addition of steroid-sparing immunosuppressive agents. Due to the distinct clinical symptoms, disease progression, implant-associated fibrosis, and resistance to therapy, the potential involvement of implants in the development of large-vessel vasculitis was considered, and a potential association with ASIA was postulated. Although there is limited evidence to support a direct link between adjuvants and the pathogenesis of TA, similarities in cellular immunity between the two conditions exist. The diagnosis of this complex and potentially debilitating condition requires a comprehensive clinical examination, laboratory evaluation, and instrumental assessment. This will aid in identifying potential contributing factors and ensuring successful treatment.
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spelling pubmed-100155232023-03-15 Takayasu arteritis associated with autoimmune/inflammatory syndrome induced by adjuvants: a case-based review Simeonova, Desislava Georgiev, Tsvetoslav Shivacheva, Tanya Rheumatol Int Case Based Review Takayasu’s arteritis (TA) is a chronic granulomatous vasculitis that predominantly affects the aorta and its major branches. Despite advancements in the understanding of the pathogenic pathways of vascular inflammation, the etiology and predisposing factors of TA remain to be fully understood. In susceptible individuals, exposure to adjuvants may trigger, unlock or unmask an autoimmune disorder, presenting as non-specific constitutional symptoms or a fully developed autoimmune syndrome such as vasculitis. Here, we hypothesize that TA could be triggered by siliconosis, a subtype of the autoimmune/inflammatory syndrome induced by adjuvants (ASIA). ASIA, also known as Shoenfeld syndrome, encompasses a wide range of autoimmune and immune-mediated diseases resulting from dysregulation of the immune response after exposure to agents with adjuvant activity. This case report describes the development of large artery vasculitis, TA, in an individual one year following the placement of silicone breast implants. The patient initially presented with non-specific symptoms, and multiple imaging methods were employed, including ultrasound diagnostics, CT angiography, and 18-fluorodeoxyglucose positron emission tomography/CT. These techniques revealed vasculitic alterations in the carotid arteries and thoracic aorta. Initial treatment with glucocorticosteroids proved ineffective, prompting the addition of steroid-sparing immunosuppressive agents. Due to the distinct clinical symptoms, disease progression, implant-associated fibrosis, and resistance to therapy, the potential involvement of implants in the development of large-vessel vasculitis was considered, and a potential association with ASIA was postulated. Although there is limited evidence to support a direct link between adjuvants and the pathogenesis of TA, similarities in cellular immunity between the two conditions exist. The diagnosis of this complex and potentially debilitating condition requires a comprehensive clinical examination, laboratory evaluation, and instrumental assessment. This will aid in identifying potential contributing factors and ensuring successful treatment. Springer Berlin Heidelberg 2023-03-15 2023 /pmc/articles/PMC10015523/ /pubmed/36920514 http://dx.doi.org/10.1007/s00296-023-05309-2 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Case Based Review
Simeonova, Desislava
Georgiev, Tsvetoslav
Shivacheva, Tanya
Takayasu arteritis associated with autoimmune/inflammatory syndrome induced by adjuvants: a case-based review
title Takayasu arteritis associated with autoimmune/inflammatory syndrome induced by adjuvants: a case-based review
title_full Takayasu arteritis associated with autoimmune/inflammatory syndrome induced by adjuvants: a case-based review
title_fullStr Takayasu arteritis associated with autoimmune/inflammatory syndrome induced by adjuvants: a case-based review
title_full_unstemmed Takayasu arteritis associated with autoimmune/inflammatory syndrome induced by adjuvants: a case-based review
title_short Takayasu arteritis associated with autoimmune/inflammatory syndrome induced by adjuvants: a case-based review
title_sort takayasu arteritis associated with autoimmune/inflammatory syndrome induced by adjuvants: a case-based review
topic Case Based Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10015523/
https://www.ncbi.nlm.nih.gov/pubmed/36920514
http://dx.doi.org/10.1007/s00296-023-05309-2
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AT shivachevatanya takayasuarteritisassociatedwithautoimmuneinflammatorysyndromeinducedbyadjuvantsacasebasedreview