A case of tubulointerstitial nephritis in IgG4-related systemic disease with markedly enlarged kidneys

4Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

IgG4-related systemic disease, including autoimmune pancreatitis, is a multi-organ disorder characterized by elevated serum immunoglobulin G4 (IgG4) concentration and IgG4-positive plasma cell infiltration. We report the case of a 67-year-old man with IgG4-related tubulointerstitial nephritis, presenting with markedly enlarged kidneys and renal dysfunction. The serum IgG4 level was elevated with 4200 mg/dl and pathological examination revealed patchy, clearly fringed areas of IgG4-positive plasma cell infiltration and advanced fibrosis in the renal parenchyma, perirenal tissue and lymph nodes. With oral prednisolone at a dose of 60 mg daily, a contraction of the kidneys and an improvement of renal function were observed. No recurrence of the disease was observed during the reduction of prednisolone to 2 mg daily over 4 years. © The Author [2009].

Cite

CITATION STYLE

APA

Mise, N., Tomizawa, Y., Fujii, A., Yamaguchi, Y., & Sugimoto, T. (2009). A case of tubulointerstitial nephritis in IgG4-related systemic disease with markedly enlarged kidneys. NDT Plus, 2(3), 233–235. https://doi.org/10.1093/ndtplus/sfp023

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free