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- Overview of IgG4-Related Tubulointerstitial Nephritis and Its Mimickers
- Hyeon Joo Jeong, Su-Jin Shin, Beom Jin Lim
- J Pathol Transl Med. 2016;50(1):26-36. Published online December 14, 2015
- DOI: https://doi.org/10.4132/jptm.2015.11.09
- 10,772 View
- 220 Download
- 12 Web of Science
- 10 Crossref
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Abstract
PDF - Tubulointerstitial nephritis (TIN) is the most common form of renal involvement in IgG4-related disease. It is characterized by a dominant infiltrate of IgG4-positive plasma cells in the interstitium and storiform fibrosis. Demonstration of IgG4-positive plasma cells is essential for diagnosis, but the number of IgG4-positive cells and the ratio of IgG4-positive/IgG-positive plasma cells may vary from case to case and depending on the methods of tissue sampling even in the same case. IgG4-positive plasma cells can be seen in TIN associated with systemic lupus erythematosus, Sjögren syndrome, or anti-neutrophil cytoplasmic antibody–associated vasculitis, which further add diagnostic confusion and difficulties. To have a more clear view of IgG4-TIN and to delineate differential points from other TIN with IgG4-positive plasma cell infiltrates, clinical and histological features of IgG4-TIN and its mimickers were reviewed. In the rear part, cases suggesting overlap of IgG4-TIN and its mimickers and glomerulonephritis associated with IgG4-TIN were briefly described.
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Citations
Citations to this article as recorded by
- IgG4-related kidney disease: Clinicopathologic features, differential diagnosis, and mimics
Sarwat I. Gilani, Alessia Buglioni, Lynn D. Cornell
Seminars in Diagnostic Pathology.2024; 41(2): 88. CrossRef - Utilizing Immunoglobulin G4 Immunohistochemistry for Risk Stratification in Patients with Papillary Thyroid Carcinoma Associated with Hashimoto Thyroiditis
Faridul Haq, Gyeongsin Park, Sora Jeon, Mitsuyoshi Hirokawa, Chan Kwon Jung
Endocrinology and Metabolism.2024; 39(3): 468. CrossRef - IgG4-assoziierte Nierenerkrankungen
Christina Thompson, Frank O. Henes, Oliver M. Steinmetz, Simon Melderis
Die Nephrologie.2023; 18(4): 249. CrossRef - Concurrent anti-neutrophil cytoplasmic antibody-associated glomerulonephritis and IgG4-associated tubulointerstitial nephritis with C3 glomerulonephritis
Jianan Feng, Jinyu Yu, Xueyao Wang, Yue Wang, Yang Liu, Zhonggao Xu, Weixia Sun
Medicine.2020; 99(5): e18857. CrossRef - A case of eosinophilic granulomatosis with polyangiitis as a mimicker of IgG4-related disease
Ryuichiro Kanda, Satoshi Kubo, Kazuhisa Nakano, Akio Kawabe, Aya Nawata, Kentaro Hanami, Shingo Nakayamada, Yoshiya Tanaka
Modern Rheumatology Case Reports.2020; 4(2): 278. CrossRef - Renal tubular acidosis as the initial presentation of Sjögren’s syndrome
Karen Ho, Pouneh Dokouhaki, Mark McIsaac, Bhanu Prasad
BMJ Case Reports.2019; 12(8): e230402. CrossRef - Immunoglobulin G4-related kidney diseases: An updated review
Maurizio Salvadori, Aris Tsalouchos
World Journal of Nephrology.2018; 7(1): 29. CrossRef - Systemic lupus erythematosus in a patient with an organic lesion of the central nervous system: practicaldifferential diagnosis
E. V. Lebedeva, M. V. Novoseltsev, A. N. Lvov, I. V. Khamaganova
Klinicheskaya dermatologiya i venerologiya.2018; 17(6): 21. CrossRef - Concurrent IgG4-related tubulointerstitial nephritis and IgG4 myeloperoxidase-anti-neutrophil cytoplasmic antibody positive crescentic glomerulonephritis
Tao Su, Li Yang, Zhao Cui, Su-xia Wang, Ming-hui Zhao
Medicine.2017; 96(20): e6707. CrossRef - IgG4-Related Kidney Disease: Report of a Case Presenting as a Renal Mass
Daniele Bianchi, Luca Topazio, Gabriele Gaziev, Valerio Iacovelli, Pierluigi Bove, Alessandro Mauriello, Enrico Finazzi Agrò
Case Reports in Surgery.2017; 2017: 1. CrossRef
- IgG4-related kidney disease: Clinicopathologic features, differential diagnosis, and mimics
Original Article
- International Society of Nephrology/Renal Pathology Society 2003 Classification of Lupus Nephritis.
- Moon Hyang Park
- Korean J Pathol. 2006;40(3):165-175.
- 2,640 View
- 191 Download
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Abstract
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- The new revised classification of glomerulonephritis in systemic lupus erythematosus under the auspice of the International Society of Nephrology and the Renal Pathology Society (ISN/ RPS) was proposed in 2003. The revised classification preserves the simplicity of the original WHO classification, incorporates selective refinements concerning activity and chronicity from the 1982 and 1995 revisions, and adds a number of new modifications. Overall, it bears a strong similarity to the 1974 classification, but introduces several important modifications concerning quantitative and qualitative differences between class III and IV lesions. The new classification provides a clear and unequivocal description of the various lesions and classes of lupus nephritis as well as definitions for diagnostic terms. This review is introduced the ISN/RPS 2003 classification which will facilitates accurate communication between pathologists and clinicians.
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