Copyright
©The Author(s) 2018.
World J Nephrol. Jan 6, 2018; 7(1): 29-40
Published online Jan 6, 2018. doi: 10.5527/wjn.v7.i1.29
Published online Jan 6, 2018. doi: 10.5527/wjn.v7.i1.29
Criterion | The Mayo Clinic criteria | JSN criteria |
Histology | Plasma cell-rich TIN with > 10 IgG4+ plasma cells/HPF in the most concentrated field (mandatory criterion) TBM immune complex deposits by immunofluorescence, immunochemistry, and/or electron microscopy | Dense lymphoplasmacytic infiltrate with > 10 IgG4+ plasma cells/HPF and/or IgG4/IgG+ plasma cell ratio of > 40%; Characteristic storiform fibrosis |
Imaging | Small peripheral low-attenuation cortical nodules, round or wedge-shaped lesions, or diffuse patchy involvement | Multiple low-density lesions or enhanced CT, diffuse kidney enlargement, hypovascular solitary nodule, hypertrophic lesion of the renal pelvic wall |
Serology | Elevated serum IgG4 or total IgG level | Elevated serum IgG4 or total IgG level |
Clinical features | None | Clinical or laboratory evidence of kidney damage |
Other organ involvement | Characteristic findings of IgG4-RD in other organs | Characteristic findings of IgG4-RD in other organs |
Definite IgG4-TIN | The histologic feature and at least one other feature from imaging, serology or other organ involvement | The histologic feature (a and b) and at least two of other features from imaging, serology or other organ involvement |
- Citation: Salvadori M, Tsalouchos A. Immunoglobulin G4-related kidney diseases: An updated review. World J Nephrol 2018; 7(1): 29-40
- URL: https://www.wjgnet.com/2220-6124/full/v7/i1/29.htm
- DOI: https://dx.doi.org/10.5527/wjn.v7.i1.29