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IgG4-related Kidney Disease--an Update

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Date 2015 Jan 17
PMID 25594543
Citations 38
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Abstract

Purpose Of Review: IgG4-related disease (IgG4-RD) is a recently recognized systemic inflammatory disorder that can affect most organs/tissues such as sarcoidosis. The kidney is a frequently affected organ with tubulointerstitial nephritis (TIN), the representative lesion of IgG4-RD. This review focuses on the latest knowledge of IgG4-related kidney disease (IgG4-RKD).

Recent Findings: A wide range of renal manifestations of IgG4-RD, that is TIN, membranous glomerulonephritis (MGN) and other glomerular lesions, and pyelitis, are collectively referred to as IgG4-RKD. Clinically, decreased renal function, or characteristic imaging findings such as multiple low-density lesions on contrast-enhanced computed tomography or diffuse thickening of the renal pelvic wall, are typical presenting features. Although a rapid response to corticosteroid therapy is a very important feature of IgG4-TIN, in cases in which renal function is moderately to severely decreased before therapy, only partial recovery of renal function is obtained.

Summary: TIN with characteristic imaging findings is a typical manifestation of IgG4-RKD in the interstitium, while MGN is a representative manifestation of the glomerular lesions. Although IgG4 is a central feature of IgG4-RD, the recent discovery of IgG4-negative IgG4-RD raises questions about the causative role of the IgG4 molecule in this context.

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References
1.
Montironi R, Scarpelli M, Cheng L, Lopez-Beltran A, Burattini M, Kirkali Z . Immunoglobulin G4-related disease in genitourinary organs: an emerging fibroinflammatory entity often misdiagnosed preoperatively as cancer. Eur Urol. 2012; 64(6):865-72. DOI: 10.1016/j.eururo.2012.11.056. View

2.
Yoshida K, Toki F, Takeuchi T, Watanabe S, Shiratori K, Hayashi N . Chronic pancreatitis caused by an autoimmune abnormality. Proposal of the concept of autoimmune pancreatitis. Dig Dis Sci. 1995; 40(7):1561-8. DOI: 10.1007/BF02285209. View

3.
Kawano M, Mizushima I, Yamaguchi Y, Imai N, Nakashima H, Nishi S . Immunohistochemical Characteristics of IgG4-Related Tubulointerstitial Nephritis: Detailed Analysis of 20 Japanese Cases. Int J Rheumatol. 2012; 2012:609795. PMC: 3415101. DOI: 10.1155/2012/609795. View

4.
Khosroshahi A, Ayalon R, Beck Jr L, Salant D, Bloch D, Stone J . IgG4-Related Disease Is Not Associated with Antibody to the Phospholipase A2 Receptor. Int J Rheumatol. 2012; 2012:139409. PMC: 3357948. DOI: 10.1155/2012/139409. View

5.
Ito K, Yamada K, Mizushima I, Aizu M, Fujii H, Mizutomi K . Henoch-Schönlein purpura nephritis in a patient with IgG4-related disease: a possible association. Clin Nephrol. 2012; 79(3):246-52. DOI: 10.5414/CN107114. View