Table 1.
Transition of the Concept of IgG4-Related Disease
| Author (Year) | Evidences/Contents |
|---|---|
| Mikulicz (1892)12 | Mikulicz’s disease (Z Chir Fesrschr) |
| Sarles et al. (1961)1 | Hypergammaglobulinemia in CP (Am J Dig Dis) |
| Comings et al. (1967)9 | Familial multifocal fibrosclerosis (Ann Intern Med) |
| Küttner (1972)13 | Küttner tumor (Beitr Klin Chir) |
| Kawaguchi et al. (1991)7 | Lymphoplasmacytic sclerosing pancreatitis (Hum Pathol) |
| Yoshida et al. (1995)2 | Autoimmune pancreatitis (Dig Dis Sci) |
| Hamano et al. (2001)4 | High IgG4 levels in sclerosing pancreatitis (N Eng J Med) |
| Kamisawa et al. (2003)8 | IgG4-related sclerosing disease (J Gastroenterol) |
| Kamisawa et al. (2006)14 | IgG4-related sclerosing disease (J Gastroenterol) |
| Yamamoto et al. (2006)15 | IgG4-related plasmacytic disease (Mod Rheumatol) |
| Masaki et al. (2009)16 | IgG4-multiorgan lymphoproliferative syndrome (MOLPS) (Ann Rheum Dis) |
| Shimosegawa et al. (2011)11 | International Consensus Diagnostic Criteria for AIP (Pancreas) |
| Umehara et al.3,17 | Concept and comprehensive diagnostic criteria for IgG4-related disease (Mod Rheumatol) |
| Deshpande et al. (2012)18 | International Pathological Consensus for IgG4-RD (Mod Pathol) |
| Stone et al. (2012)19 | Nomenclatures of individual organ manifestation of IgG4-RD (Arthritis Rheum) |
CP, chronic pancreatitis; AIP, autoimmune pancreatitis.