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Sjögren’s Syndrome and Silicosis – a Case Report
Sjögren’s syndrome is an autoimmune disease of unknown etiology where immune response to self-antigens is believed to result from interactions between genetic and environmental factors. We describe the case of a patient who has been diagnosed with Sjögren’s syndrome based on typical clinical and imm...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Institute of Immunobiology and Human Genetics
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4877877/ https://www.ncbi.nlm.nih.gov/pubmed/27275245 http://dx.doi.org/10.3889/oamjms.2015.043 |
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author | Plavsic, Aleksandra Miskovic, Rada Bolpacic, Jasna Šuštran, Branka Peric-Popadic, Aleksandra Bogic, Mirjana |
author_facet | Plavsic, Aleksandra Miskovic, Rada Bolpacic, Jasna Šuštran, Branka Peric-Popadic, Aleksandra Bogic, Mirjana |
author_sort | Plavsic, Aleksandra |
collection | PubMed |
description | Sjögren’s syndrome is an autoimmune disease of unknown etiology where immune response to self-antigens is believed to result from interactions between genetic and environmental factors. We describe the case of a patient who has been diagnosed with Sjögren’s syndrome based on typical clinical and immunological parameters. The clinical picture was dominated by the respiratory symptoms, and radiographic and multislice computed tomography examination of the chest showed certain changes characteristic of pneumoconiosis. Given that the patient has worked in a foundry where he has been exposed to the silica dust, he was subject to examination by occupational health specialists under the suspicion of lung silicosis, who confirmed the silicosis. This case report points to the possible connection between a professional exposure to silica and Sjögren’s syndrome. Occupational exposure to silica is a possible risk factor for the development of autoimmune diseases, and in the evaluation of patients with connective tissue diseases it is important to consider work-related history. |
format | Online Article Text |
id | pubmed-4877877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Institute of Immunobiology and Human Genetics |
record_format | MEDLINE/PubMed |
spelling | pubmed-48778772016-06-06 Sjögren’s Syndrome and Silicosis – a Case Report Plavsic, Aleksandra Miskovic, Rada Bolpacic, Jasna Šuštran, Branka Peric-Popadic, Aleksandra Bogic, Mirjana Open Access Maced J Med Sci Case Report Sjögren’s syndrome is an autoimmune disease of unknown etiology where immune response to self-antigens is believed to result from interactions between genetic and environmental factors. We describe the case of a patient who has been diagnosed with Sjögren’s syndrome based on typical clinical and immunological parameters. The clinical picture was dominated by the respiratory symptoms, and radiographic and multislice computed tomography examination of the chest showed certain changes characteristic of pneumoconiosis. Given that the patient has worked in a foundry where he has been exposed to the silica dust, he was subject to examination by occupational health specialists under the suspicion of lung silicosis, who confirmed the silicosis. This case report points to the possible connection between a professional exposure to silica and Sjögren’s syndrome. Occupational exposure to silica is a possible risk factor for the development of autoimmune diseases, and in the evaluation of patients with connective tissue diseases it is important to consider work-related history. Institute of Immunobiology and Human Genetics 2015-06-15 2015-04-23 /pmc/articles/PMC4877877/ /pubmed/27275245 http://dx.doi.org/10.3889/oamjms.2015.043 Text en Copyright: © 2015 Aleksandra Plavsic, Rada Miskovic, Jasna Bolpacic, Branka Šuštran, Aleksandra Peric-Popadic, Mirjana Bogic. http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Case Report Plavsic, Aleksandra Miskovic, Rada Bolpacic, Jasna Šuštran, Branka Peric-Popadic, Aleksandra Bogic, Mirjana Sjögren’s Syndrome and Silicosis – a Case Report |
title | Sjögren’s Syndrome and Silicosis – a Case Report |
title_full | Sjögren’s Syndrome and Silicosis – a Case Report |
title_fullStr | Sjögren’s Syndrome and Silicosis – a Case Report |
title_full_unstemmed | Sjögren’s Syndrome and Silicosis – a Case Report |
title_short | Sjögren’s Syndrome and Silicosis – a Case Report |
title_sort | sjögren’s syndrome and silicosis – a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4877877/ https://www.ncbi.nlm.nih.gov/pubmed/27275245 http://dx.doi.org/10.3889/oamjms.2015.043 |
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