Abstract
Tubulointerstitial nephritis (TIN) is a disease pattern with heterogeneous causes. Recently a specific subtype of autoimmune TIN, IgG4-related TIN, has been identified that is part of systemic IgG4-related disease/ autoimmune pancreatitis. On biopsy, this TIN shows an IgG4 plasma cell-rich infiltrate, akin to the pancreatic tissue findings in autoimmune pancreatitis, and may show tubulointerstitial immune complex deposits. Notably, some cases may be mass-forming. Recognition of this specific type of TIN can guide appropriate patient therapy.
Original language | English (US) |
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Pages (from-to) | 951-953 |
Number of pages | 3 |
Journal | Kidney international |
Volume | 78 |
Issue number | 10 |
DOIs |
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State | Published - Nov 2010 |
ASJC Scopus subject areas
- Nephrology