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Coronary artery disease concomitant with immunoglobulin G4-related disease: a case report and literature review
BACKGROUND: Immunoglobulin G4-related disease (IgG4-RD) is an autoimmune condition associated with high serum IgG4 levels which was first reported as autoimmune pancreatitis in 2001. Since then, many additional organs, such as bile duct, salivary gland, retroperitoneal organs, and liver, have been r...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6439393/ https://www.ncbi.nlm.nih.gov/pubmed/31020256 http://dx.doi.org/10.1093/ehjcr/ytz013 |
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author | Okuyama, Toraaki Tanaka, Toshikazu D Nagoshi, Tomohisa Yoshimura, Michihiro |
author_facet | Okuyama, Toraaki Tanaka, Toshikazu D Nagoshi, Tomohisa Yoshimura, Michihiro |
author_sort | Okuyama, Toraaki |
collection | PubMed |
description | BACKGROUND: Immunoglobulin G4-related disease (IgG4-RD) is an autoimmune condition associated with high serum IgG4 levels which was first reported as autoimmune pancreatitis in 2001. Since then, many additional organs, such as bile duct, salivary gland, retroperitoneal organs, and liver, have been reported with high serum IgG4 levels in cases of IgG4-RD. However, evidence of the relationship between IgG4-RD and coronary artery disease (CAD) has been scare. Here, we report a case of CAD concomitant with IgG4-RD. CASE SUMMARY: A 74-year-old man was referred to our hospital with a chief complaint of chest pain and was admitted. The patient was found to have had a myocardial infarction with ST-segment elevation and underwent an emergent percutaneous coronary intervention. Owing to a rapidly increased blood glucose level, computed tomography was performed and showed autoimmune pancreatitis. An elevated serum level of IgG4 led to a diagnosis of IgG4-RD involving acute coronary syndrome (ACS). DISCUSSION: Cardiac involvement in IgG4-RD has been reported; however, cases of ACS concomitant with IgG4-RD are rare. Our report suggests that CAD, specifically ACS, can coexist in patients with IgG4-RD. Therefore, cases of concomitant CAD and IgG4-RD should be accurately diagnosed and evidence should be collected to elucidate the mechanism and characteristics of this condition. |
format | Online Article Text |
id | pubmed-6439393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64393932019-04-24 Coronary artery disease concomitant with immunoglobulin G4-related disease: a case report and literature review Okuyama, Toraaki Tanaka, Toshikazu D Nagoshi, Tomohisa Yoshimura, Michihiro Eur Heart J Case Rep Case Reports BACKGROUND: Immunoglobulin G4-related disease (IgG4-RD) is an autoimmune condition associated with high serum IgG4 levels which was first reported as autoimmune pancreatitis in 2001. Since then, many additional organs, such as bile duct, salivary gland, retroperitoneal organs, and liver, have been reported with high serum IgG4 levels in cases of IgG4-RD. However, evidence of the relationship between IgG4-RD and coronary artery disease (CAD) has been scare. Here, we report a case of CAD concomitant with IgG4-RD. CASE SUMMARY: A 74-year-old man was referred to our hospital with a chief complaint of chest pain and was admitted. The patient was found to have had a myocardial infarction with ST-segment elevation and underwent an emergent percutaneous coronary intervention. Owing to a rapidly increased blood glucose level, computed tomography was performed and showed autoimmune pancreatitis. An elevated serum level of IgG4 led to a diagnosis of IgG4-RD involving acute coronary syndrome (ACS). DISCUSSION: Cardiac involvement in IgG4-RD has been reported; however, cases of ACS concomitant with IgG4-RD are rare. Our report suggests that CAD, specifically ACS, can coexist in patients with IgG4-RD. Therefore, cases of concomitant CAD and IgG4-RD should be accurately diagnosed and evidence should be collected to elucidate the mechanism and characteristics of this condition. Oxford University Press 2019-02-18 /pmc/articles/PMC6439393/ /pubmed/31020256 http://dx.doi.org/10.1093/ehjcr/ytz013 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the European Society of Cardiology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Case Reports Okuyama, Toraaki Tanaka, Toshikazu D Nagoshi, Tomohisa Yoshimura, Michihiro Coronary artery disease concomitant with immunoglobulin G4-related disease: a case report and literature review |
title | Coronary artery disease concomitant with immunoglobulin G4-related disease: a case report and literature review |
title_full | Coronary artery disease concomitant with immunoglobulin G4-related disease: a case report and literature review |
title_fullStr | Coronary artery disease concomitant with immunoglobulin G4-related disease: a case report and literature review |
title_full_unstemmed | Coronary artery disease concomitant with immunoglobulin G4-related disease: a case report and literature review |
title_short | Coronary artery disease concomitant with immunoglobulin G4-related disease: a case report and literature review |
title_sort | coronary artery disease concomitant with immunoglobulin g4-related disease: a case report and literature review |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6439393/ https://www.ncbi.nlm.nih.gov/pubmed/31020256 http://dx.doi.org/10.1093/ehjcr/ytz013 |
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