No abstract available.
Cholangitis, Sclerosing*

No abstract available.
Cholangitis, Sclerosing* ; Diagnosis* ; Immunoglobulins*

No abstract available.
Cholangitis*

No abstract available.
Cholangitis*

Cholangitis, Sclerosing ; diagnosis ; therapy ; Humans

No abstract available.
Cholangitis, Sclerosing ; Critical Illness ; Humans

Immunoglobulin G4-related disease (IgG4-RD) is a systemic fibroinflammatory condition of which IgG4-related sclerosing cholangitis (IgG4-SC) is the biliary manifestation. In this review, we provide an overview of IgG4-RD, with a focus on the biliary manifestations. In particular, we describe the important differential diagnoses of IgG4-SC, namely, primary sclerosing cholangitis and cholangiocarcinoma, outline diagnostic criteria for IgG4-SC, provide insight into possible pathophysiological mechanisms underlying the disease and discuss short and long-term management options of this recently described disease.
Cholangiocarcinoma ; Cholangitis, Sclerosing* ; Diagnosis, Differential ; Immunoglobulins*

Primary sclerosing cholangitis, a chronic cholestatic liver disease, is uncommon and is characterized byinflammation and fibrosis of the bile ducts. It frequently occurs in association with ulcerative colitis. Wedescribe two cases of primary sclerosing cholangitis in patients with ulcerative colitis.
Bile Ducts ; Cholangitis ; Cholangitis, Sclerosing* ; Colitis, Ulcerative* ; Fibrosis ; Humans ; Liver Diseases ; Ulcer*

Cholangitis ; classification ; diagnosis ; etiology ; Cholangitis, Sclerosing ; diagnosis ; Diagnosis, Differential ; Humans ; Immunoglobulin G

Primary sclerosing cholangitis (PSC) is a rare disease entity. The medical therapy for PSC has not been reasonably beneficial. Thus liver transplantation is known to be the ultimate therapy. Because liver transplantation for PSC has been performed rarely in Korea, we report a case of liver transplantation for PSC with a review of the literature. A 35-year-old male was admitted to our hospital with recurrent jaundice for seven years. ERCP showed multiple strictures of intrahepatic duct and an irregularity of the extrahepatic duct wall. Despite medication and endoscopic treatment, liver functions did not imporve and clinical status got worsened. Thus liver transplantation was performed for the correction of hepatic failure. Two months after transplantation, liver functions and general weakness gradually improved and now, one year after liver transplantation, the patient is in normal life.
Adult ; Cholangitis, Sclerosing/diagnosis/*surgery ; Humans ; *Liver Transplantation ; Male