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Large vessel vasculopathy in a patient with systemic lupus erythematosus: a case report
BACKGROUND: Vasculopathy in systemic lupus erythematosus is a rare form of vascular involvement characterized by non-inflammatory vascular injury with the accumulation of immune complexes in the walls of the arteries, resulting in luminal narrowing. While previous reports have demonstrated vasculiti...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6588931/ https://www.ncbi.nlm.nih.gov/pubmed/31227015 http://dx.doi.org/10.1186/s13256-019-2126-4 |
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author | Waki, Daisuke Onishi, Akira Morinobu, Akio |
author_facet | Waki, Daisuke Onishi, Akira Morinobu, Akio |
author_sort | Waki, Daisuke |
collection | PubMed |
description | BACKGROUND: Vasculopathy in systemic lupus erythematosus is a rare form of vascular involvement characterized by non-inflammatory vascular injury with the accumulation of immune complexes in the walls of the arteries, resulting in luminal narrowing. While previous reports have demonstrated vasculitis in the large vessels or vasculopathy in the small vessels, vasculopathy in large vessels has not yet been reported. CASE PRESENTATION: We present the case of a 43-year-old Japanese woman with peripheral large vessel vasculopathy associated with systemic lupus erythematosus. She presented a 7-year history of progressive headaches and intermittent claudication, although she had no atherosclerotic risk factors. Vascular ultrasonography and enhanced computed tomography showed multiple vascular stenoses and occlusion. The histological findings of her left temporal artery revealed narrowing of the lumen caused by intimal thickening without inflammatory cells and the deposition of immunoglobulin G, complement component 3, and fibrinogen in the wall of the intima. Beraprost and cilostazol improved arterial occlusion without immunosuppressive therapy. CONCLUSIONS: Large vessel vasculopathy should be considered another potential cause of arterial stenoses and occlusion in patients with lupus when they have peripheral arterial disease despite having no atherosclerotic risk factors. |
format | Online Article Text |
id | pubmed-6588931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65889312019-07-08 Large vessel vasculopathy in a patient with systemic lupus erythematosus: a case report Waki, Daisuke Onishi, Akira Morinobu, Akio J Med Case Rep Case Report BACKGROUND: Vasculopathy in systemic lupus erythematosus is a rare form of vascular involvement characterized by non-inflammatory vascular injury with the accumulation of immune complexes in the walls of the arteries, resulting in luminal narrowing. While previous reports have demonstrated vasculitis in the large vessels or vasculopathy in the small vessels, vasculopathy in large vessels has not yet been reported. CASE PRESENTATION: We present the case of a 43-year-old Japanese woman with peripheral large vessel vasculopathy associated with systemic lupus erythematosus. She presented a 7-year history of progressive headaches and intermittent claudication, although she had no atherosclerotic risk factors. Vascular ultrasonography and enhanced computed tomography showed multiple vascular stenoses and occlusion. The histological findings of her left temporal artery revealed narrowing of the lumen caused by intimal thickening without inflammatory cells and the deposition of immunoglobulin G, complement component 3, and fibrinogen in the wall of the intima. Beraprost and cilostazol improved arterial occlusion without immunosuppressive therapy. CONCLUSIONS: Large vessel vasculopathy should be considered another potential cause of arterial stenoses and occlusion in patients with lupus when they have peripheral arterial disease despite having no atherosclerotic risk factors. BioMed Central 2019-06-22 /pmc/articles/PMC6588931/ /pubmed/31227015 http://dx.doi.org/10.1186/s13256-019-2126-4 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Waki, Daisuke Onishi, Akira Morinobu, Akio Large vessel vasculopathy in a patient with systemic lupus erythematosus: a case report |
title | Large vessel vasculopathy in a patient with systemic lupus erythematosus: a case report |
title_full | Large vessel vasculopathy in a patient with systemic lupus erythematosus: a case report |
title_fullStr | Large vessel vasculopathy in a patient with systemic lupus erythematosus: a case report |
title_full_unstemmed | Large vessel vasculopathy in a patient with systemic lupus erythematosus: a case report |
title_short | Large vessel vasculopathy in a patient with systemic lupus erythematosus: a case report |
title_sort | large vessel vasculopathy in a patient with systemic lupus erythematosus: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6588931/ https://www.ncbi.nlm.nih.gov/pubmed/31227015 http://dx.doi.org/10.1186/s13256-019-2126-4 |
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