Review Article

Are Classification Criteria for IgG4-RD Now Possible? The Concept of IgG4-Related Disease and Proposal of Comprehensive Diagnostic Criteria in Japan

Table 1

Nomenclatures of IgG4-related conditions.

NomenclatureAuthors(year)

IgG4-related autoimmune diseaseKamisawa et al. [1](2003)
IgG4-associated multifocal systemic fibrosisvan der Vliet and Perenboom [2](2004)
IgG4-related systemic diseaseKamisawa et al. [3](2004)
IgG4-related sclerosing diseaseKamisawa et al. [4ā€“7](2006)
Hyper-IgG4 diseaseNeild et al. [8](2006)
IgG4-related diseaseZen et al. [9](2007)
Systemic IgG4 plasmacytic syndrome (SIPS)Masaki et al. [10](2009)
IgG4-related multiorgan Lymphoproliferative syndrome (IgG4-MOLPS)Masaki et al. [10](2009)
IgG4-associated diseaseGeyer et al. [11](2010)