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Erschienen in: Pediatric Nephrology 4/2017

07.05.2016 | Educational Review

Tubulointerstitial nephritis: diagnosis, treatment, and monitoring

verfasst von: Emily Joyce, Paulina Glasner, Sarangarajan Ranganathan, Agnieszka Swiatecka-Urban

Erschienen in: Pediatric Nephrology | Ausgabe 4/2017

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Abstract

Tubulointerstitial nephritis (TIN) is a frequent cause of acute kidney injury (AKI) that can lead to chronic kidney disease (CKD). TIN is associated with an immune-mediated infiltration of the kidney interstitium by inflammatory cells, which may progress to fibrosis. Patients often present with nonspecific symptoms, which can lead to delayed diagnosis and treatment of the disease. Etiology can be drug-induced, infectious, idiopathic, genetic, or related to a systemic inflammatory condition such as tubulointerstitial nephritis and uveitis (TINU) syndrome, inflammatory bowel disease, or immunoglobulin G4 (IgG4)-associated immune complex multiorgan autoimmune disease (MAD). It is imperative to have a high clinical suspicion for TIN in order to remove potential offending agents and treat any associated systemic diseases. Treatment is ultimately dependent on underlying etiology. While there are no randomized controlled clinical trials to assess treatment choice and efficacy in TIN, corticosteroids have been a mainstay of therapy, and recent studies have suggested a possible role for mycophenolate mofetil. Urinary biomarkers such as alpha1- and beta2-microglobulin may help diagnose and monitor disease activity in TIN. Screening for TIN should be implemented in children with inflammatory bowel disease, uveitis, or IgG4-associated MAD.
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Metadaten
Titel
Tubulointerstitial nephritis: diagnosis, treatment, and monitoring
verfasst von
Emily Joyce
Paulina Glasner
Sarangarajan Ranganathan
Agnieszka Swiatecka-Urban
Publikationsdatum
07.05.2016
Verlag
Springer Berlin Heidelberg
Erschienen in
Pediatric Nephrology / Ausgabe 4/2017
Print ISSN: 0931-041X
Elektronische ISSN: 1432-198X
DOI
https://doi.org/10.1007/s00467-016-3394-5

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