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Comparison of clinicopathological features between patients with and without hypocomplementemia in IgG4-related kidney disease.

Authors :
Saeki, Takako
Nagasawa, Tasuku
Ubara, Yoshifumi
Taniguchi, Yoshinori
Yanagita, Motoko
Nishi, Shinichi
Nagata, Michio
Yamaguchi, Yutaka
Saito, Takao
Nakashima, Hitoshi
Kawano, Mitsuhiro
Source :
Nephrology Dialysis Transplantation. Apr2023, Vol. 38 Issue 4, p1053-1056. 4p.
Publication Year :
2023

Abstract

However, several radiologically characteristic lesions within the kidney have also been shown to be diagnostic for IgG4-RD affecting the kidney [[2]], and several glomerular lesions (especially membranous glomerulonephritis [[3]]) have been described as associated with IgG4-RD. Therefore the term "IgG4-related kidney disease" (IgG4-RKD) has been proposed as a comprehensive term for the renal lesions associated with IgG4-RD [[4]]. All of them were classified as having definite or probable IgG4-RKD according to the diagnostic criteria for IgG4-RKD 2020 [[9]] and/or as definite IgG4-RD according to the 2019 ACR/EULAR classification criteria [[2]]. [Extracted from the article]

Details

Language :
English
ISSN :
09310509
Volume :
38
Issue :
4
Database :
Academic Search Index
Journal :
Nephrology Dialysis Transplantation
Publication Type :
Academic Journal
Accession number :
162858632
Full Text :
https://doi.org/10.1093/ndt/gfac317