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Immunoglobulin G4-related sclerosing disease

A recently described mass-forming lesion that occurs in the pancreas, submandibular glands, lacrimal glands, lymph nodes, and hepatobiliary tract. It is characterized by the presence of marked tissue sclerosis and infiltration by numerous plasma cells. The plasma cells show immunohistochemical staining for IgG4 and the serum IgG4 levels are often increased.

30 trials tagged with this condition →

Autoimmune pancreatitis 3 trials Sub-types →
IgG4-related kidney disease 1 trial
IgG4-related retroperitoneal fibrosis 1 trial Sub-types →
IgG4-related aortitis 0 trials
IgG4-related mediastinitis 0 trials
IgG4-related mesenteritis 0 trials
IgG4-related ophthalmic disorder 0 trials Sub-types →
IgG4-related pachymeningitis 0 trials
IgG4-related sclerosing cholangitis 0 trials
IgG4-related submandibular gland disease 0 trials
IgG4-related thyroid disease 0 trials
Cutaneous pseudolymphoma 0 trials
Eosinophilic angiocentric fibrosis 0 trials
Primary cutaneous plasmacytosis 0 trials