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. 2018 May;14(5):293–304.

Table 2.

Causes of Secondary Sclerosing Cholangitis and Mimics of PSC

Infectious Causes AIDS cholangiopathy (eg, Cryptosporidium parvum, cytomegalovirus)
Helminthic infection (eg, Clonorchis, Opisthorchis, Ascaris)
Recurrent pyogenic cholangitis (also referred to as oriental cholangio-hepatitis)
Intrinsic or Extrinsic Compressive Causes (Benign or Malignant) Mirizzi syndrome
Cholangiocarcinoma
Diffuse intrahepatic malignancy
Compressive lymphadenopathy
Portal hypertensive biliopathy
Postoperative strictures
Chronic pancreatitis
Immunologic Causes IgG4-associated cholangiopathy
Eosinophilic cholangitis
Mast cell cholangiopathy
Histiocytosis X
Systemic vasculitis
Hepatic allograft rejection
Primary biliary cholangitis
Ischemic Causes Posttransplant nonanastomotic strictures
Postintraarterial chemotherapy
Postradiation therapy
Congenital and/or Idiopathic Causes Choledochal cyst (eg, Caroli disease)
Progressive familial intrahepatic cholestasis

IgG4, immunoglobulin G subclass 4; PSC, primary sclerosing cholangitis.