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- W2175991667 abstract "We have read with great interest the recently published article entitled “IgG4-related systemic disease with coronary arteritis and aortitis, causing recurring critical coronary ischemia” written by Tran MN and his colleagues [ [1] Tran M.N. Langguth D. Hart G. et al. IgG4-related systemic disease with coronary arteritis and aortitis, causing recurring critical coronary ischemia. Int. J. Cardiol. 2015; 201: 33-34 Abstract Full Text Full Text PDF PubMed Scopus (17) Google Scholar ]. This paper described a 72 year old male with complex presentation of IgG4-related disease (IgG4-RD) with aortitis and coronary arteritis. IgG4-RD is a systemic immune-mediated disease characterized pathologically by the infiltration of IgG4-bearing plasma cells into involved organs and raised IgG4 levels [ [2] Stone J.H. Zen Y. Deshpande V. IgG4-RD. N. Engl. J. Med. 2012; 366: 539-551 Crossref PubMed Scopus (1873) Google Scholar ]. The cardinal clinical feature of IgG4-RD is single or multiple organ swelling and the organs more frequently involved are the pancreas, salivary/lacrimal glands, biliary tree, kidneys, thyroid gland, lungs, and aorta [ [3] Brito-Zerón P. Ramos-Casals M. Bosch X. et al. The clinical spectrum of IgG4-related disease. Autoimmun. Rev. 2014; 13: 1203-1210 Crossref PubMed Scopus (198) Google Scholar ]." @default.
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- W2175991667 date "2016-11-01" @default.
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- W2175991667 title "IgG4-related disease with coronary arteritis" @default.
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- W2175991667 doi "https://doi.org/10.1016/j.ijcard.2015.10.144" @default.
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