Rationale: While primary sclerosing cholangitis (PSC) has been recognized for decades,
immunoglobulin G4-related sclerosing cholangitis (IgG4-SC) has been correctly diagnosed …

Immunoglobin G4-related sclerosing cholangitis (IgG4-SC) is recognized as one of the
systemic sclerosing diseases characterized by abundant IgG4-positive plasma cells with …

IgG4-related sclerosing cholangitis (IgG4-SC) is a biliary tract manifestation of IgG4-related
diseases (IgG4-RDs). A recent epidemiological study in Japan demonstrated that the point …

Background Recent research has shown that a substantial number of patients with primary
sclerosing cholangitis (PSC) can also have elevated serum/tissue IgG4. The aim of our study …

Primary sclerosing cholangitis (PSC) is a chronic progressive liver disease. Sub-types of
PSC have been described, most recently PSC with elevated serum and/or tissue IgG4 …

There is increased interest and recognition of the clinical variants of Sclerosing Cholangitis
(SC) namely IgG4-SC, PSC/AIH overlap and PSC. For most Centers, the characteristic of …

Background The long-term outcomes of immunoglobulin G4-related sclerosing cholangitis
(IgG4-SC) are not well known. Methods The outcomes of patients with IgG4-SC at Mayo …

Background. Immunoglobulin IgG4‐associated cholangitis (IAC) disease is a systemic
disease histologically characterized by extensive T lymphocytes and IgG4 positive plasma …

Sclerosing cholangitis is heterogeneous in its etiopathogenesis. Recently, sclerosing
cholangitis showing abundant immunoglobulin (Ig) G4+ plasma cell infiltration was added to …

According to recent guidelines, primary sclerosing cholangitis (PSC) is diagnosed when a
patient has a cholestatic liver enzyme profile, characteristic bile duct changes on imaging …