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      Case Report: Predominant Tubulointerstitial Lupus Nephritis or the Combination With IgG4-Related Disease?

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          Abstract

          Isolated or dominant tubulointerstitial lupus nephritis is rare. Here, we reported a 67-year-old man diagnosed with systemic lupus erythematosus (SLE) based on clinical and laboratory criteria, who was showing impaired renal function and non-nephrotic range proteinuria in the past 2 years. Renal biopsy showed almost normal glomeruli, but the tubulointerstitium showed “storiform” pattern with interstitial infiltration of IgG3 predominant plasma cells. Immunofluorescence showed linear and granular staining of IgG and C1q along TBM and interstitium. He started on medium dose of oral steroids and mycophenolate mofetil, which were gradually tapered. As a result, his renal function improved over a few days. Now, he continued on low dose steroids and mycophenolate mofetil with no evidence of relapse.

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          Most cited references22

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          2016 American College of Rheumatology/European League Against Rheumatism classification criteria for primary Sjögren's syndrome: A consensus and data-driven methodology involving three international patient cohorts.

          To develop and validate an international set of classification criteria for primary Sjögren's syndrome (SS) using guidelines from the American College of Rheumatology (ACR) and the European League Against Rheumatism (EULAR). These criteria were developed for use in individuals with signs and/or symptoms suggestive of SS.
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            Comprehensive diagnostic criteria for IgG4-related disease (IgG4-RD), 2011

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              The 2019 American College of Rheumatology/European League Against Rheumatism classification criteria for IgG4-related disease

              IgG4-related disease (IgG4-RD) can cause fibroinflammatory lesions in nearly any organ. Correlation among clinical, serological, radiological and pathological data is required for diagnosis. This work was undertaken to develop and validate an international set of classification criteria for IgG4-RD. An international multispecialty group of 86 physicians was assembled by the American College of Rheumatology (ACR) and the European League Against Rheumatism (EULAR). Investigators used consensus exercises; existing literature; derivation and validation cohorts of 1879 subjects (1086 cases, 793 mimickers); and multicriterion decision analysis to identify, weight and test potential classification criteria. Two independent validation cohorts were included. A three-step classification process was developed. First, it must be demonstrated that a potential IgG4-RD case has involvement of at least one of 11 possible organs in a manner consistent with IgG4-RD. Second, exclusion criteria consisting of a total of 32 clinical, serological, radiological and pathological items must be applied; the presence of any of these criteria eliminates the patient from IgG4-RD classification. Third, eight weighted inclusion criteria domains, addressing clinical findings, serological results, radiological assessments and pathological interpretations, are applied. In the first validation cohort, a threshold of 20 points had a specificity of 99.2% (95% CI 97.2% to 99.8%) and a sensitivity of 85.5% (95% CI 81.9% to 88.5%). In the second, the specificity was 97.8% (95% CI 93.7% to 99.2%) and the sensitivity was 82.0% (95% CI 77.0% to 86.1%). The criteria were shown to have robust test characteristics over a wide range of thresholds. ACR/EULAR classification criteria for IgG4-RD have been developed and validated in a large cohort of patients. These criteria demonstrate excellent test performance and should contribute substantially to future clinical, epidemiological and basic science investigations.
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                Author and article information

                Contributors
                Journal
                Front Med (Lausanne)
                Front Med (Lausanne)
                Front. Med.
                Frontiers in Medicine
                Frontiers Media S.A.
                2296-858X
                28 June 2021
                2021
                : 8
                : 684889
                Affiliations
                [1] 1Renal Division, Department of Medicine, Peking University First Hospital , Beijing, China
                [2] 2Institute of Nephrology, Peking University , Beijing, China
                [3] 3Key Laboratory of Renal Disease, Ministry of Health of China , Beijing, China
                [4] 4Key Laboratory of CKD Prevention and Treatment, Ministry of Education of China , Beijing, China
                [5] 5Research Units of Diagnosis and Treatment of Immune-mediated Kidney Diseases, Chinese Academy of Medical Sciences , Beijing, China
                [6] 6The Second People's Hospital of Shanxi Province , Shanxi, China
                [7] 7Laboratory of Electron Microscopy, Pathological Center, Peking University First Hospital , Beijing, China
                [8] 8Peking-Tsinghua Center for Life Sciences , Beijing, China
                Author notes

                Edited by: Sergey Brodsky, Ohio State University Hospital, United States

                Reviewed by: Beom Jin Lim, Yonsei University College of Medicine, South Korea; Samy Hakroush, University of Göttingen, Germany

                *Correspondence: Ming-hui Zhao mhzhao@ 123456bjmu.edu.cn

                This article was submitted to Nephrology, a section of the journal Frontiers in Medicine

                †These authors have contributed equally to this work

                Article
                10.3389/fmed.2021.684889
                8273166
                34262916
                0bba282c-9b22-48bd-9e3b-1fd7362e94f1
                Copyright © 2021 Tan, Qin, Yu, Xu, Wang, Zhou and Zhao.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 24 March 2021
                : 27 May 2021
                Page count
                Figures: 1, Tables: 1, Equations: 0, References: 22, Pages: 5, Words: 3422
                Categories
                Medicine
                Case Report

                systemic lupus erythematosus,lupus nephritis,predominant interstitial nephritis,igg3,storiform pattern

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